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    Food & Materials Purchasing Coordinator  

    - Des Plaines
    Job Title: Food & Materials Purchasing Coordinator Job Location: Des... Read More

    Job Title: Food & Materials Purchasing Coordinator
    Job Location: Des Plaines-USA-60016
    Work Location Type: On-Site
    Salary Range: $14.25 - 22.27 per hour

    About us

    LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.

    Role Purpose Statement

    Responsible for purchasing materials for the Materials department from suppliers; ensure orders are accurate and complete in a timely manner.

    Main Accountabilities

    Principal Duties and Responsibilities:
    • Determine quantity of food products to order based on forecast, on hand inventory, lead-time, and supplier delivery schedule
    • Create purchase orders
    • Reconcile purchase order against supplier invoices and what is in system
    • Conduct daily/weekly/monthly inventory using order guides and EOM process
    • Communicate with supplier regarding order and pricing discrepancies
    • Determine product overages/stockouts and communicate to manager; assist with reallocation or substitution of product
    • Responsible for days on hand (DOH)
    • Ensure addresses are up to date in the purchasing system
    • Assist the Materials department on other projects as needed
    • Perform other duties and responsibilities as assigned by management

    Knowledge, Skills and Experience

    • High school diploma or general education degree (GED)
    • One to three years materials, purchasing, and/or clerical experience required
    • SAP MM experience preferred
    • Strong interpersonal/communication skills
    • Must be able to perform in a high stress environment
    • Strong organizational skills
    • Basic knowledge of Microsoft office programs
    • Intermediate math skills (add, subtract, multiply, divide)
    • Must be available to work nights, weekends, and holidays as needed

    LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

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    Transportation Coordinator-ORD Hourly  

    - Des Plaines
    Job Title: Transportation Coordinator-ORD Hourly Job Location: Des Pl... Read More

    Job Title: Transportation Coordinator-ORD Hourly
    Job Location: Des Plaines-USA-60016
    Work Location Type: On-Site
    Salary Range: $18.00 - 23.50 per hour

    About us

    LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.

    Role Purpose Statement

    Provide support to the Operations team by ensuring compliance across Quality, Safety, Transportation, and Security. Collaborate closely with the Transportation team to maintain daily staffing levels and ensure appropriate operational coverage.

    Main Accountabilities

    Safety, Security & Quality Compliance

    Safety, Security & Quality Compliance

    Support and administer Transportation requirements to ensure LSG Sky Chefs protocols are met, including maintaining appropriate staffing levels. Participate in required training to remain current with OVC-established compliance standards across all key compliance areas. Work collaboratively with Operations Management to communicate deficiencies and ensure consistent application of policies and procedures. Maintain all required documentation within key areas of compliance in accordance with established company standards. Proactively support other departments and functions as a Subject Matter Expert for compliance-related matters. Knowledge, Skills and Experience Prior experience in compliance and record keeping functions with a demonstrated understanding of staffing processes is required. Excellent communication skills with the ability to effectively engage with employees at all levels. Experience in Food Safety or Food Science is a plus. Associate's degree or a certification in a compliance related field preferred. Strong analytical, organizational, and problem-solving skills with exceptional attention to detail. Strong Excel skills and the ability to quickly become proficient in supporting software platforms. Team oriented individual who works well collaboratively. Must be avaialble to work rotating shifts that include, morning, afternoons, evenings, weekends and holidays.

    LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

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    Buyer Coordinator - Airline Catering HOURLY Position  

    - Lockhart
    Job Title: Buyer Coordinator - Airline Catering HOURLY Position Job L... Read More

    Job Title: Buyer Coordinator - Airline Catering HOURLY Position
    Job Location: Austin-USA-78719
    Work Location Type: On-Site
    Salary Range: $20.00 - 22.40 per hour

    About us

    LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.

    Position Overview

    We are seeking a highly organized and proactive Buyer Coordinator to support our fast-paced airline catering operations. This position is based in our Austin, TX Customer Service Center (CSC) servicing multiple airlines and charter flights. You will be responsible for sourcing and developing the supply chain for designated goods and services. The Buyer Coordinator also provides ongoing tactical procurement support for product transitions and updates related to non-strategic materials. This position requires a fast learner who is comfortable navigating proprietary systems, working with Excel, and effectively communicating across all departments.

    Work hours: 40-hour work week + occassional overtime Work schedule: 5 consecutive work days + 2 consecutive days off. Must be available to work a flexible, non-traditional schedule (including weekends) as needed, as operations demands vary Work location: Sky Chefs facility near Austin-Bergstrom International Airport What You'll Do Monitor inventory levels and initiate timely purchasing to ensure all operational departments are adequately stocked. Source and coordinate procurement of goods and services, ensuring adherence to customer specifications and cost parameters. Collaborate with internal teams (i.e. culinary, transportation, production) to understand sourcing needs and timelines. Track product line changes and adjust procurement plans as needed to meet customer and operational requirements. Evaluate supplier performance and escalate issues when necessary. Identify and onboard qualified vendors who meet company standards. Partner with Program Management and other internal stakeholders to ensure items are compliant and cost-effective. Support supply chain initiatives that drive standardization and year-over-year cost savings. Accurately maintain procurement data in SAP and internal proprietary systems. Use Excel and other tools to track order status, vendor performance, and purchasing trends. Provide reporting and insights to support inventory planning and operations. Act as a liaison between departments and procurement to ensure real-time support for operational needs. Communicate proactively to resolve order issues, shipment delays, or supply shortages. Contribute to a culture of continuous improvement and cross-functional teamwork What We Look for in a Candidate 1+ years of purchasing or related field experience required or inventory coordination experience in a fast-paced environment; operations or production facility experience strongly preferred. Bachelor's degree in Supply Chain, Business, or related field preferred. Strong Excel skills required; experience with SAP or ERP systems is a plus. Ability to learn and navigate proprietary systems quickly. Excellent organization, time management, and communication skills. Ability to work flexible hours as needed to meet operational demands. Demonstrated problem-solving skills and attention to detail Strong analytical skills for evaluating data

    LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

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    Buyer Coordinator - Airline Catering HOURLY Position  

    - Pflugerville
    Job Title: Buyer Coordinator - Airline Catering HOURLY Position Job L... Read More

    Job Title: Buyer Coordinator - Airline Catering HOURLY Position
    Job Location: Austin-USA-78719
    Work Location Type: On-Site
    Salary Range: $20.00 - 22.40 per hour

    About us

    LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.

    Position Overview

    We are seeking a highly organized and proactive Buyer Coordinator to support our fast-paced airline catering operations. This position is based in our Austin, TX Customer Service Center (CSC) servicing multiple airlines and charter flights. You will be responsible for sourcing and developing the supply chain for designated goods and services. The Buyer Coordinator also provides ongoing tactical procurement support for product transitions and updates related to non-strategic materials. This position requires a fast learner who is comfortable navigating proprietary systems, working with Excel, and effectively communicating across all departments.

    Work hours: 40-hour work week + occassional overtime Work schedule: 5 consecutive work days + 2 consecutive days off. Must be available to work a flexible, non-traditional schedule (including weekends) as needed, as operations demands vary Work location: Sky Chefs facility near Austin-Bergstrom International Airport What You'll Do Monitor inventory levels and initiate timely purchasing to ensure all operational departments are adequately stocked. Source and coordinate procurement of goods and services, ensuring adherence to customer specifications and cost parameters. Collaborate with internal teams (i.e. culinary, transportation, production) to understand sourcing needs and timelines. Track product line changes and adjust procurement plans as needed to meet customer and operational requirements. Evaluate supplier performance and escalate issues when necessary. Identify and onboard qualified vendors who meet company standards. Partner with Program Management and other internal stakeholders to ensure items are compliant and cost-effective. Support supply chain initiatives that drive standardization and year-over-year cost savings. Accurately maintain procurement data in SAP and internal proprietary systems. Use Excel and other tools to track order status, vendor performance, and purchasing trends. Provide reporting and insights to support inventory planning and operations. Act as a liaison between departments and procurement to ensure real-time support for operational needs. Communicate proactively to resolve order issues, shipment delays, or supply shortages. Contribute to a culture of continuous improvement and cross-functional teamwork What We Look for in a Candidate 1+ years of purchasing or related field experience required or inventory coordination experience in a fast-paced environment; operations or production facility experience strongly preferred. Bachelor's degree in Supply Chain, Business, or related field preferred. Strong Excel skills required; experience with SAP or ERP systems is a plus. Ability to learn and navigate proprietary systems quickly. Excellent organization, time management, and communication skills. Ability to work flexible hours as needed to meet operational demands. Demonstrated problem-solving skills and attention to detail Strong analytical skills for evaluating data

    LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

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    Buyer Coordinator - Airline Catering HOURLY Position  

    - Del Valle
    Job Title: Buyer Coordinator - Airline Catering HOURLY Position Job L... Read More

    Job Title: Buyer Coordinator - Airline Catering HOURLY Position
    Job Location: Austin-USA-78719
    Work Location Type: On-Site
    Salary Range: $20.00 - 22.40 per hour

    About us

    LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.

    Position Overview

    We are seeking a highly organized and proactive Buyer Coordinator to support our fast-paced airline catering operations. This position is based in our Austin, TX Customer Service Center (CSC) servicing multiple airlines and charter flights. You will be responsible for sourcing and developing the supply chain for designated goods and services. The Buyer Coordinator also provides ongoing tactical procurement support for product transitions and updates related to non-strategic materials. This position requires a fast learner who is comfortable navigating proprietary systems, working with Excel, and effectively communicating across all departments.

    Work hours: 40-hour work week + occassional overtime Work schedule: 5 consecutive work days + 2 consecutive days off. Must be available to work a flexible, non-traditional schedule (including weekends) as needed, as operations demands vary Work location: Sky Chefs facility near Austin-Bergstrom International Airport What You'll Do Monitor inventory levels and initiate timely purchasing to ensure all operational departments are adequately stocked. Source and coordinate procurement of goods and services, ensuring adherence to customer specifications and cost parameters. Collaborate with internal teams (i.e. culinary, transportation, production) to understand sourcing needs and timelines. Track product line changes and adjust procurement plans as needed to meet customer and operational requirements. Evaluate supplier performance and escalate issues when necessary. Identify and onboard qualified vendors who meet company standards. Partner with Program Management and other internal stakeholders to ensure items are compliant and cost-effective. Support supply chain initiatives that drive standardization and year-over-year cost savings. Accurately maintain procurement data in SAP and internal proprietary systems. Use Excel and other tools to track order status, vendor performance, and purchasing trends. Provide reporting and insights to support inventory planning and operations. Act as a liaison between departments and procurement to ensure real-time support for operational needs. Communicate proactively to resolve order issues, shipment delays, or supply shortages. Contribute to a culture of continuous improvement and cross-functional teamwork What We Look for in a Candidate 1+ years of purchasing or related field experience required or inventory coordination experience in a fast-paced environment; operations or production facility experience strongly preferred. Bachelor's degree in Supply Chain, Business, or related field preferred. Strong Excel skills required; experience with SAP or ERP systems is a plus. Ability to learn and navigate proprietary systems quickly. Excellent organization, time management, and communication skills. Ability to work flexible hours as needed to meet operational demands. Demonstrated problem-solving skills and attention to detail Strong analytical skills for evaluating data

    LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

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    Job Title: Buyer Coordinator - Airline Catering HOURLY Position Job L... Read More

    Job Title: Buyer Coordinator - Airline Catering HOURLY Position
    Job Location: Austin-USA-78719
    Work Location Type: On-Site
    Salary Range: $20.00 - 22.40 per hour

    About us

    LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.

    Position Overview

    We are seeking a highly organized and proactive Buyer Coordinator to support our fast-paced airline catering operations. This position is based in our Austin, TX Customer Service Center (CSC) servicing multiple airlines and charter flights. You will be responsible for sourcing and developing the supply chain for designated goods and services. The Buyer Coordinator also provides ongoing tactical procurement support for product transitions and updates related to non-strategic materials. This position requires a fast learner who is comfortable navigating proprietary systems, working with Excel, and effectively communicating across all departments.

    Work hours: 40-hour work week + occassional overtime Work schedule: 5 consecutive work days + 2 consecutive days off. Must be available to work a flexible, non-traditional schedule (including weekends) as needed, as operations demands vary Work location: Sky Chefs facility near Austin-Bergstrom International Airport What You'll Do Monitor inventory levels and initiate timely purchasing to ensure all operational departments are adequately stocked. Source and coordinate procurement of goods and services, ensuring adherence to customer specifications and cost parameters. Collaborate with internal teams (i.e. culinary, transportation, production) to understand sourcing needs and timelines. Track product line changes and adjust procurement plans as needed to meet customer and operational requirements. Evaluate supplier performance and escalate issues when necessary. Identify and onboard qualified vendors who meet company standards. Partner with Program Management and other internal stakeholders to ensure items are compliant and cost-effective. Support supply chain initiatives that drive standardization and year-over-year cost savings. Accurately maintain procurement data in SAP and internal proprietary systems. Use Excel and other tools to track order status, vendor performance, and purchasing trends. Provide reporting and insights to support inventory planning and operations. Act as a liaison between departments and procurement to ensure real-time support for operational needs. Communicate proactively to resolve order issues, shipment delays, or supply shortages. Contribute to a culture of continuous improvement and cross-functional teamwork What We Look for in a Candidate 1+ years of purchasing or related field experience required or inventory coordination experience in a fast-paced environment; operations or production facility experience strongly preferred. Bachelor's degree in Supply Chain, Business, or related field preferred. Strong Excel skills required; experience with SAP or ERP systems is a plus. Ability to learn and navigate proprietary systems quickly. Excellent organization, time management, and communication skills. Ability to work flexible hours as needed to meet operational demands. Demonstrated problem-solving skills and attention to detail Strong analytical skills for evaluating data

    LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

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    Director of Operations  

    - Des Plaines
    Job Title: Director of Operations Job Location: Des Plaines-USA-60016... Read More

    Job Title: Director of Operations
    Job Location: Des Plaines-USA-60016
    Work Location Type: On-Site
    Salary Range: Salary: $126,015 - $169.958

    About us

    LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.

    Role Purpose Statement We are seeking a dynamic, hands on Director of Operations who thrives in fast-paced environments and is passionate about leading large teams, optimizing processes, and driving performance at scale. If you're energized by operational complexity and inspired by the challenge of delivering excellence every single day, this is your opportunity to make an impact at a flagship operation.


    Main Accountabilities

    Business Strategy, Policies and Tools

    Execute the implementation of the CSC planning Ensure compliance with the policies provided by CSC and Corporate

    Managing Business

    Provide data for the development of an annual business plan and budgeting for the CSC Implement the short -term manufacturing (or operation) planning in coordination with other relevant interfaces. Ensure efficient and timely corrective actions in case of significant deviations Oversee the CSC economic and operating performance. Ensure that the CSC is managed and controlled efficiently in line with the company's framework and market requirements. Ensure optimal deployment of human, technical and material resources in the CSC Ensure the ordering of all materials needed at the CSC Ensure that the CSC work methods are in line with the company's standards and customer contracts Initiate Capex requests Initiate and control continuous optimization of processes Ensure the compliance with safety, health, environmental and quality guidelines provided by Corporate and local regula tions and customer requirements Ensure clear communication and close cooperation with all relevant internal and external interfaces

    Leadership

    Ensure that the area of responsibility is properly organized, staffed and directed Guide, motivate and develop the subordinate employees within the Human Resources Policy Participates in coaching the expanded Global Performance System (GPS) process, as well as additional career development activities to enhance the effectiveness and potential of the team Make the company's values and management principles live in the department(s) Plan / Implement and control the cost budget in the area of responsibility; initiate and steer corrective actions in case of deviations Participate and support company sponsored initiatives such as Global Quality Standard (GQS), Hazard Analysis and Critical Control Points (HACCP), Lean Manufacturing, Employee Safety
    Knowledge, Skills and Experience Bachelor's degree in Operations, Business, Supply Chain, or related field 5+ years of senior operations leadership experience in manufacturing, food service, aviation, logistics, or similar high-output environments Proven ability to lead large teams in a dynamic, multi shift operation Strong knowledge of safety and regulatory compliance (FAA, OSHA, FDA, USDA) Experience managing P&L, budgets, and operational KPIs Lean, Six Sigma, or continuous improvement experience Preferred Experience in airline catering or aviation services Background in operational transformation or large scale process optimization

    LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

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    Job Title: Buyer Coordinator - Airline Catering HOURLY Position Job L... Read More

    Job Title: Buyer Coordinator - Airline Catering HOURLY Position
    Job Location: Austin-USA-78719
    Work Location Type: On-Site
    Salary Range: $20.00 - 22.40 per hour

    About us

    LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.

    Position Overview

    We are seeking a highly organized and proactive Buyer Coordinator to support our fast-paced airline catering operations. This position is based in our Austin, TX Customer Service Center (CSC) servicing multiple airlines and charter flights. You will be responsible for sourcing and developing the supply chain for designated goods and services. The Buyer Coordinator also provides ongoing tactical procurement support for product transitions and updates related to non-strategic materials. This position requires a fast learner who is comfortable navigating proprietary systems, working with Excel, and effectively communicating across all departments.

    Work hours: 40-hour work week + occassional overtime Work schedule: 5 consecutive work days + 2 consecutive days off. Must be available to work a flexible, non-traditional schedule (including weekends) as needed, as operations demands vary Work location: Sky Chefs facility near Austin-Bergstrom International Airport What You'll Do Monitor inventory levels and initiate timely purchasing to ensure all operational departments are adequately stocked. Source and coordinate procurement of goods and services, ensuring adherence to customer specifications and cost parameters. Collaborate with internal teams (i.e. culinary, transportation, production) to understand sourcing needs and timelines. Track product line changes and adjust procurement plans as needed to meet customer and operational requirements. Evaluate supplier performance and escalate issues when necessary. Identify and onboard qualified vendors who meet company standards. Partner with Program Management and other internal stakeholders to ensure items are compliant and cost-effective. Support supply chain initiatives that drive standardization and year-over-year cost savings. Accurately maintain procurement data in SAP and internal proprietary systems. Use Excel and other tools to track order status, vendor performance, and purchasing trends. Provide reporting and insights to support inventory planning and operations. Act as a liaison between departments and procurement to ensure real-time support for operational needs. Communicate proactively to resolve order issues, shipment delays, or supply shortages. Contribute to a culture of continuous improvement and cross-functional teamwork What We Look for in a Candidate 1+ years of purchasing or related field experience required or inventory coordination experience in a fast-paced environment; operations or production facility experience strongly preferred. Bachelor's degree in Supply Chain, Business, or related field preferred. Strong Excel skills required; experience with SAP or ERP systems is a plus. Ability to learn and navigate proprietary systems quickly. Excellent organization, time management, and communication skills. Ability to work flexible hours as needed to meet operational demands. Demonstrated problem-solving skills and attention to detail Strong analytical skills for evaluating data

    LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

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    Buyer Coordinator - Airline Catering HOURLY Position  

    - Austin
    Job Title: Buyer Coordinator - Airline Catering HOURLY Position Job L... Read More

    Job Title: Buyer Coordinator - Airline Catering HOURLY Position
    Job Location: Austin-USA-78719
    Work Location Type: On-Site
    Salary Range: $20.00 - 22.40 per hour

    About us

    LSG Sky Chefs is one of the world's largest airline catering and hospitality providers, known for its outstanding reputation and dynamic approach in the industry. Voted "Airline Caterer of the Year in North America" for 2023 and 2024, we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America.

    Position Overview

    We are seeking a highly organized and proactive Buyer Coordinator to support our fast-paced airline catering operations. This position is based in our Austin, TX Customer Service Center (CSC) servicing multiple airlines and charter flights. You will be responsible for sourcing and developing the supply chain for designated goods and services. The Buyer Coordinator also provides ongoing tactical procurement support for product transitions and updates related to non-strategic materials. This position requires a fast learner who is comfortable navigating proprietary systems, working with Excel, and effectively communicating across all departments.

    Work hours: 40-hour work week + occassional overtime Work schedule: 5 consecutive work days + 2 consecutive days off. Must be available to work a flexible, non-traditional schedule (including weekends) as needed, as operations demands vary Work location: Sky Chefs facility near Austin-Bergstrom International Airport What You'll Do Monitor inventory levels and initiate timely purchasing to ensure all operational departments are adequately stocked. Source and coordinate procurement of goods and services, ensuring adherence to customer specifications and cost parameters. Collaborate with internal teams (i.e. culinary, transportation, production) to understand sourcing needs and timelines. Track product line changes and adjust procurement plans as needed to meet customer and operational requirements. Evaluate supplier performance and escalate issues when necessary. Identify and onboard qualified vendors who meet company standards. Partner with Program Management and other internal stakeholders to ensure items are compliant and cost-effective. Support supply chain initiatives that drive standardization and year-over-year cost savings. Accurately maintain procurement data in SAP and internal proprietary systems. Use Excel and other tools to track order status, vendor performance, and purchasing trends. Provide reporting and insights to support inventory planning and operations. Act as a liaison between departments and procurement to ensure real-time support for operational needs. Communicate proactively to resolve order issues, shipment delays, or supply shortages. Contribute to a culture of continuous improvement and cross-functional teamwork What We Look for in a Candidate 1+ years of purchasing or related field experience required or inventory coordination experience in a fast-paced environment; operations or production facility experience strongly preferred. Bachelor's degree in Supply Chain, Business, or related field preferred. Strong Excel skills required; experience with SAP or ERP systems is a plus. Ability to learn and navigate proprietary systems quickly. Excellent organization, time management, and communication skills. Ability to work flexible hours as needed to meet operational demands. Demonstrated problem-solving skills and attention to detail Strong analytical skills for evaluating data

    LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

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    Quality Assurance/EHS Supervisor  

    - Watertown
    Overview: Primo Brands is a leading branded beverage company in North... Read More
    Overview: Primo Brands is a leading branded beverage company in North America with a focus on healthy hydration. We are proud to offer an extensive and iconic portfolio of highly recognizable, sustainably sourced, and conveniently packaged branded beverages distributed across more than 150,000 retail outlets.

    We are currently seeking a Quality Assurance/EHS Supervisor. For the Quality/Safety Health and Environmental Compliance Supervisor role, this position involves leading the Food Safety Program and managing a team of Quality Assurance Technicians to ensure adherence to food safety, quality, and regulatory standards. You'll partner with cross-functional teams in planning, production, maintenance, and warehousing to maximize operational efficiency.

    If you are a current associate of Primo Brands, please apply via myADP.

    Base Salary: $107,101-$119,916 . This role is eligible for an annual bonus.

    Location: Watertown, CT

    Benefits of working for Primo Brands:

    Health Benefits: Medical, prescription, dental, vision, flexible spending account (FSA), dependent care flexible spending account (FSA), health savings account (HSA)

    Retirement/Investing:

    401K with a 5% match, Employee Stock Purchase Plan (ESPP)

    Insurance: Employee Life Insurance, short and long-term disability, critical illness, hospital indemnity, accident insurance, spouse/domestic partner/child life insurance, accidental death and dismemberment

    Other great benefits: Employee discounts, save on auto, home, and pet insurance, tuition reimbursement, paid vacation and sick time, 9 paid holidays and 3 paid floating holidays, paid leave for when you have a baby, adopt a child, or become a foster parent, legal services, identity theft protection, employee assistance program (EAP), adoption reimbursement benefit, FEDlogic, commuter benefits

    Responsibilities: Lead and train two shifts of operations team members to achieve quality metrics in a manner consistent with our culture and values Lead two shifts of operations both first and second shifts Supervise one direct report in the QA Tech position Partner with the Planning, Production, Maintenance and Warehouse teams to maximize results Implement and maintain Safety/Environmental programs appropriately and within budgetary limits Manage budgeting, purchasing, and inventory of plant operating supplies for quality and safety Lead all company and local quality/safety initiatives, audits, local SHE awareness & compliance while also meeting key performance indicators (KPIs) Track, analyze, and lead initiatives for all quality and customer complaint issues within the plant Use continuous improvement methodologies and projects to improve and streamline processes Ensure plant compliance and record retention in accordance with current federal, state, and local legislation on good hygiene practices, good manufacturing practices (GMP's), HACCP, NFPA, OSHA and EPA Ensure compliance and record keeping for all mandated quality checks, testing, sampling, and sanitation activities Support and maintain site-specific manuals, records of inspections, and incidents relating to Safety, Health, Security and Environment Offer expertise and assistance in managing the plant water sources and monitor over-fill and water usage reporting Cultivate relationships with local law enforcement, local fire department, and other emergency services to provide harmonious working relationships in the community Lead incident investigations, monitor incident root cause & corrective actions for issues such as fire, hazardous materials, unsafe situations, security issues and/or non-compliance issues to prevent recurrence Provide training and onboarding for new hires and factory employees as it relates to QA and Safety Additional duties as assigned. Qualifications: Bachelor's degree in chemistry or biology or equivalent combination of education and/or experience Three or more years of experience in quality assurance within clean (food, bev, pharma) manufacturing and two or more years of experience in a supervisory capacity Three or more years of experience in a workplace safety, security, and environmental programs Understanding of quality testing and standards within the food and beverage industry to include analytical, microbiological, and sensory Demonstrated application of Good Laboratory Practices (GLP's) and knowledge of GMP's A minimum of 2 years of administration and compliance with State/Federal OSHA, EPA, and local Air Quality Management District Knowledge of Statistical Process Control, HACCP, sanitation, and hygienic design Familiarity with quality and hygiene regulations as it relates to FDA and state requirements preferred. Knowledge and exposure to Six Sigma, and various problem-solving methodologies needed, TPM exposure preferred. Strong computer skills, including Word, Excel, PowerPoint, and business management software (SAP preferred) Ability to manage multiple projects and initiatives on tight deadlines and delegate accordingly. Effective communication skills with the ability to influence change and encourage action. Solid problem-solving abilities with the ability to coach and mentor others in this capacity. Demonstrated track record of developing employees. Ability and willingness to respond to after-hours calls for critical issues and provide weekend coverage a few times/year. Knowledge of principles, procedures, and standards for the receiving, handling, storage, shipment, and disposal of hazardous chemicals and materials. Knowledge of the nature and usage of a wide range of fire prevention, safety, health protection, and environmental protection equipment If you're ready to embark on an exciting journey with Primo Brands, apply now!

    Salary Range Disclaimer:

    The salary range provided for this position is an approximation based on market research, internal compensation data and the candidate's qualifications and experience. Final salary offers are determined through a comprehensive evaluation of candidate qualifications and may vary depending on factors such as skills, experience, and geographic location of the position. Other components of the compensation package, including benefits and bonuses, will also be considered. We are committed to fair and equitable compensation practices, and we encourage open dialogue about compensation during the interview process.

    Primo Brands' established portfolio includes billion-dollar brands Poland Spring and Pure Life , premium brands like Saratoga and Mountain Valley , regional leaders such as Arrowhead , Deer Park , Ice Mountain Ozarka , and Zephyrhills , purified brands, Primo Water and Sparkletts , and flavored and enhanced brands like Splash and AC+ION . Our extensive direct-to-consumer offerings and industry-leading line-up of innovative water dispensers create consumer connectivity through recurring water purchases across Water Direct, Water Exchange, and Water Refill. At Primo Brands, our more than 11,000 associates are at the heart of what we do and deliver on our mission to provide healthy hydration to consumers wherever, however and whenever they want it. We believe in fostering a respectful culture, which values our associates who are deeply invested in quality hydration, our communities, and the sustainability of our packaging and water sources for generations to come.

    Primo Brands is proud to be an Equal Opportunity and Affirmative Action employer, seeking to create a welcoming and diverse environment. We do not discriminate based on race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state, and local law.

    Candidates must possess strong English language skills to effectively communicate with customers and provide exceptional service. Proficiency in English is essential for understanding customer needs, resolving inquiries, and collaborating with team members.

    Read Less
  • P

    Production Lead  

    - Watertown
    Overview: Primo Brands is a leading branded beverage company in North... Read More
    Overview:

    Primo Brands is a leading branded beverage company in North America with a focus on healthy hydration. We are proud to offer an extensive and iconic portfolio of highly recognizable, sustainably sourced, and conveniently packaged branded beverages distributed across more than 150,000 retail outlets.

    If you are a current associate of Primo Brands, please apply here

    Compensation: $28.00/hour

    Location: Watertown, CT

    Shift: Monday to Friday 1:00pm-9:30pm

    Shift Differential: 6%-8% of the base hourly rate for applicable hours worked

    Additional Compensation: Two $0.50 increases-first after 90 days, second after 180 days.

    Responsibilities:

    The Team Leader Production role is responsible for teaching, training and driving performance within a factory. The Team Leader will report to the production resource who will provide direction and guidance for the respected shift. This role will serve as relief where needed and also be responsible to provide back up to the production resource. The Team Leader will coordinate with support departments, such as maintenance and quality; ensure goal alignment and proactive employee responsible for the following but not limited to complete end of shift reporting, updating production schedule when necessary, SAP related activity, lead/coach floor Shift Hand Offs, be and active participant daily ops review and facilitate all other duties as assigned by senior leadership.

    Responsibilities

    • Provide frontline leadership in day-to-day operations of getting bottles out the door safely and in accordance with quality standards.
    • Assist, as needed, during any safety issues and quality hold situations.
    • Develop team capability through training, coaching, role-modeling & assists Production Resource with managing skills matrix.
    • Leads onboarding process for new employees.
    • Enable effective communication by strengthening the use of standardized documentation & communication.
    • Ability to identify process failures when they happen and coach the team through problem solving.
    • Coordinate with business unit leaders to plan and manage the day to day allocation of resources (equipment, people, materials and systems)
    • Coach, mentor and develop team members to meet current and future business requirements.
    • Build relationships with frontline team members, colleagues and support services to ensure team-goal alignment.
    • Create and maintain a safe and positive work environment
    • Understand and adhere to internal/external regulations, procedures & policies
    • Actively pursue quality standards, specifically HAACP and GMP's
    • Review daily measures coordinate resources to drive business results
    • Communicate with planning and floor personnel ensure daily schedule changes and line management
    • Other duties as assigned by leadership

    Qualifications: Advanced understanding of at least 3 machine centers. Can effectively troubleshoot common faults. Ability to assist with changeovers, advanced CILs, PMs. Effective & impactful communication skills. Basic computer skills and ability to coach others in the creation of standards/OPL's/Maps. Ability to build relationships as a trustworthy & fair team member. At least 6 months in current internal position with fully completed & executed bootcamp/step-up-card.

    Primo Brands' established portfolio includes billion-dollar brands Poland Spring and Pure Life , premium brands like Saratoga and Mountain Valley , regional leaders such as Arrowhead , Deer Park , Ice Mountain Ozarka , and Zephyrhills , purified brands, Primo Water and Sparkletts , and flavored and enhanced brands like Splash and AC+ION . Our extensive direct-to-consumer offerings and industry-leading line-up of innovative water dispensers create consumer connectivity through recurring water purchases across Water Direct, Water Exchange, and Water Refill. At Primo Brands, our more than 11,000 associates are at the heart of what we do and deliver on our mission to provide healthy hydration to consumers wherever, however and whenever they want it. We believe in fostering a respectful culture, which values our associates who are deeply invested in quality hydration, our communities, and the sustainability of our packaging and water sources for generations to come.

    Primo Brands is proud to be an Equal Opportunity and Affirmative Action employer, seeking to create a welcoming and diverse environment. We do not discriminate based on race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state, and local law.

    Candidates must possess strong English language skills to effectively communicate with customers and provide exceptional service. Proficiency in English is essential for understanding customer needs, resolving inquiries, and collaborating with team members .

    Read Less
  • G

    Plasma Center Quality Manager  

    - Houston
    table.MiTabla max-width: 1020px;!important Would you like to join an i... Read More
    table.MiTabla max-width: 1020px;!important Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

    Quality Systems Manager (QSM)

    $3000 SIGN ON BONUS

    PRIMARY RESPONSIBILITIES: Evaluates processes, develops action plans, and coordinates the strategic implementation of quality system processes and corrective actions at the plasma donor center. Maintains oversight of the center's quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties. Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. Maintains oversight of center training program by ensuring compliance to program requirements promoting staff competency in their assigned job duties. Maintains and audits training records and files. Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained. Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks. Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required. Continuously assesses, promotes, and improves the effectiveness of quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations. Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Investigates identified trends and performs follow-up on corrective and preventative actions, system implementations, and process improvement plans to measure/determine effectiveness. Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation and authorizes final shipment. Performs a review of the documentation of unsuitable test results and unit lookback information. Performs a review of donor adverse event reports and the applicable related documentation. Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as required) is completed, documented, and on file. Performs employee training observations to ensure staff competency prior to releasing employees to work independently. Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-conformance. Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves of deferred donor reinstatement activities. Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented. Holds monthly Quality Meeting to communicate status updates and manage action outcomes.
    JOB REQUIREMENTS: Bachelor of Science degree or equivalent. Equivalency: Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an associate degree with 6 years of experience, or a master's degree with 2 years of experience. Typically requires 2 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood preferred.

    KNOWLEDGE, SKILLS, AND ABILITIES:

    Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.

    Occupational Demands Form # 6: Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32 degrees F, miscellaneous production chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

    Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals.

    Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues.

    Ability to apply abstract principles to solve complex conceptual issues.

    BENEFITS:

    We offer benefits including medical, PTO, up to 5% 401K match, and tuition reimbursement. We are committed to offering our employees opportunities for professional growth and career progression. Even though we are a global healthcare company with employees in 30 countries, Grifols prides itself on its family-like culture. Our company has more than tripled its workforce in the last 10 years - we're growing, and you can grow with us!

    Third Party Agency and Recruiter Notice:

    Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

    Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

    Location: NORTH AMERICA : USA : TX-Houston:USBEL - Houston TX-W Bellfort-BIO

    Learn more about Grifols

    Read Less
  • G

    Quality Manager for Plasma Center  

    - Lake Benton
    table.MiTabla max-width: 1020px;!important Would you like to join an... Read More
    table.MiTabla max-width: 1020px;!important
    Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

    We're Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit!

    If you enjoy working in an environment built around teamwork and trust, then consider furthering your career with us as a QUALITY SYSTEMS MANAGER ! Please read on

    Job Title: QUALITY SYSTEMS MANAGER

    SIGN-ON BONUS: $8,000 (30% at 6th month anniversary and 70% at 1st year anniversary)

    Summary:

    Evaluates processes, develops action plans, and coordinates the strategic implementation of system processes and corrective actions at the plasma donor center. Reports to the Regional Quality Manager.

    Primary Responsibilities for Role: Maintains oversight of the center's quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties. Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained. Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks. Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required. Continuously assesses, promotes, and improves the effectiveness of the quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations. Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Investigates identified trends and performs follow-up on corrective and preventive actions, system implementations, and process improvement plans to measure/determine effectiveness. Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment. Performs a review of the documentation of unsuitable test results and unit lookback information. Performs a review of donor adverse event reports and the applicable related documents. Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as may be required) is completed, documented, and on file. Performs employee training observations to ensure staff competency prior to releasing employees to work independently. Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-compliance. Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves deferred donor reinstatement activities. Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues. Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented. Holds monthly Quality Meeting to communicate status updates and manage action outcomes.
    Other Responsibilities for Role: Leads projects and initiatives as requested.
    This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.

    Job Requirements:

    EDUCATION: Bachelor of Science degree or equivalent. Certified and proficient in quality and compliance. EXPERIENCE: Typically requires 2-5 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood. EQUIVALENCY:

    Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

    KNOWLEDGE, SKILLS & ABILITIES:

    Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.

    Occupational Demands:

    Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32 , miscellaneous production Chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.

    "We are looking to grow our teams with people who share our energy and enthusiasm for creating the best experience for our donors/customers."

    Third Party Agency and Recruiter Notice:

    Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

    EEO:

    Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

    Location: NORTH AMERICA : USA : SD-Brookings

    Center Address: nd Ave South, Brookings, SD 57006

    Contact: Alex S. Contreras, Senior Talent Acquisition Partner -

    Learn more about Grifols Follow us on . click apply for full job details Read Less
  • G

    Quality Manager for Plasma Center  

    - Rexburg
    table.MiTabla max-width: 1020px;!important Would you like to join an... Read More
    table.MiTabla max-width: 1020px;!important
    Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

    We're Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit!

    If you enjoy working in an environment built around teamwork and trust, then consider furthering your career with us as a QUALITY SYSTEMS MANAGER ! Please read on

    Job Title: QUALITY SYSTEMS MANAGER

    Summary:

    Evaluates processes, develops action plans, and coordinates the strategic implementation of system processes and corrective actions at the plasma donor center. Reports to the Regional Quality Manager.

    Primary Responsibilities for Role: Maintains oversight of the center's quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties. Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained. Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks. Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required. Continuously assesses, promotes, and improves the effectiveness of the quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations. Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Investigates identified trends and performs follow-up on corrective and preventive actions, system implementations, and process improvement plans to measure/determine effectiveness. Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment. Performs a review of the documentation of unsuitable test results and unit lookback information. Performs a review of donor adverse event reports and the applicable related documents. Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as may be required) is completed, documented, and on file. Performs employee training observations to ensure staff competency prior to releasing employees to work independently. Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-compliance. Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves deferred donor reinstatement activities. Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues. Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented. Holds monthly Quality Meeting to communicate status updates and manage action outcomes.
    Other Responsibilities for Role: Leads projects and initiatives as requested.
    This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.

    Job Requirements:

    EDUCATION: Bachelor of Science degree or equivalent. Certified and proficient in quality and compliance. EXPERIENCE: Typically requires 2-5 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood. EQUIVALENCY:

    Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

    KNOWLEDGE, SKILLS & ABILITIES:

    Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.

    Occupational Demands:

    Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32 , miscellaneous production Chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.

    "We are looking to grow our teams with people who share our energy and enthusiasm for creating the best experience for our donors/customers."

    Third Party Agency and Recruiter Notice:

    Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

    EEO:

    Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

    Location: NORTH AMERICA : USA : ID-Rexburg

    Center Address: 18 E Main St, Rexburg, ID 83440

    Contact: Alex S. Contreras, Senior Talent Acquisition Partner -

    Learn more about Grifols Follow us on Facebook: Follow us on LinkedIn: . click apply for full job details Read Less
  • G

    Quality Manager for Plasma Center  

    - Toronto
    table.MiTabla max-width: 1020px;!important Would you like to join an... Read More
    table.MiTabla max-width: 1020px;!important
    Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

    We're Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit!

    If you enjoy working in an environment built around teamwork and trust, then consider furthering your career with us as a QUALITY SYSTEMS MANAGER ! Please read on

    Job Title: QUALITY SYSTEMS MANAGER

    SIGN-ON BONUS: $8,000 (30% at 6th month anniversary and 70% at 1st year anniversary)

    Summary:

    Evaluates processes, develops action plans, and coordinates the strategic implementation of system processes and corrective actions at the plasma donor center. Reports to the Regional Quality Manager.

    Primary Responsibilities for Role: Maintains oversight of the center's quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties. Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained. Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks. Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required. Continuously assesses, promotes, and improves the effectiveness of the quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations. Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Investigates identified trends and performs follow-up on corrective and preventive actions, system implementations, and process improvement plans to measure/determine effectiveness. Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment. Performs a review of the documentation of unsuitable test results and unit lookback information. Performs a review of donor adverse event reports and the applicable related documents. Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as may be required) is completed, documented, and on file. Performs employee training observations to ensure staff competency prior to releasing employees to work independently. Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-compliance. Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves deferred donor reinstatement activities. Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues. Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented. Holds monthly Quality Meeting to communicate status updates and manage action outcomes.
    Other Responsibilities for Role: Leads projects and initiatives as requested.
    This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.

    Job Requirements:

    EDUCATION: Bachelor of Science degree or equivalent. Certified and proficient in quality and compliance. EXPERIENCE: Typically requires 2-5 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood. EQUIVALENCY:

    Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

    KNOWLEDGE, SKILLS & ABILITIES:

    Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.

    Occupational Demands:

    Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32 , miscellaneous production Chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.

    "We are looking to grow our teams with people who share our energy and enthusiasm for creating the best experience for our donors/customers."

    Third Party Agency and Recruiter Notice:

    Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

    EEO:

    Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

    Location: NORTH AMERICA : USA : SD-Brookings

    Center Address: nd Ave South, Brookings, SD 57006

    Contact: Alex S. Contreras, Senior Talent Acquisition Partner -

    Learn more about Grifols Follow us on . click apply for full job details Read Less
  • G

    Quality Manager for Plasma Center  

    - Brookings
    table.MiTabla max-width: 1020px;!important Would you like to join an... Read More
    table.MiTabla max-width: 1020px;!important
    Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

    We're Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit!

    If you enjoy working in an environment built around teamwork and trust, then consider furthering your career with us as a QUALITY SYSTEMS MANAGER ! Please read on

    Job Title: QUALITY SYSTEMS MANAGER

    SIGN-ON BONUS: $8,000 (30% at 6th month anniversary and 70% at 1st year anniversary)

    Summary:

    Evaluates processes, develops action plans, and coordinates the strategic implementation of system processes and corrective actions at the plasma donor center. Reports to the Regional Quality Manager.

    Primary Responsibilities for Role: Maintains oversight of the center's quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties. Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained. Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks. Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required. Continuously assesses, promotes, and improves the effectiveness of the quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations. Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Investigates identified trends and performs follow-up on corrective and preventive actions, system implementations, and process improvement plans to measure/determine effectiveness. Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment. Performs a review of the documentation of unsuitable test results and unit lookback information. Performs a review of donor adverse event reports and the applicable related documents. Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as may be required) is completed, documented, and on file. Performs employee training observations to ensure staff competency prior to releasing employees to work independently. Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-compliance. Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves deferred donor reinstatement activities. Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues. Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented. Holds monthly Quality Meeting to communicate status updates and manage action outcomes.
    Other Responsibilities for Role: Leads projects and initiatives as requested.
    This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.

    Job Requirements:

    EDUCATION: Bachelor of Science degree or equivalent. Certified and proficient in quality and compliance. EXPERIENCE: Typically requires 2-5 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood. EQUIVALENCY:

    Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

    KNOWLEDGE, SKILLS & ABILITIES:

    Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.

    Occupational Demands:

    Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32 , miscellaneous production Chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.

    "We are looking to grow our teams with people who share our energy and enthusiasm for creating the best experience for our donors/customers."

    Third Party Agency and Recruiter Notice:

    Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

    EEO:

    Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

    Location: NORTH AMERICA : USA : SD-Brookings

    Center Address: nd Ave South, Brookings, SD 57006

    Contact: Alex S. Contreras, Senior Talent Acquisition Partner -

    Learn more about Grifols Follow us on . click apply for full job details Read Less
  • G

    Quality Manager for Plasma Center  

    - Sinai
    table.MiTabla max-width: 1020px;!important Would you like to join an... Read More
    table.MiTabla max-width: 1020px;!important
    Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

    We're Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit!

    If you enjoy working in an environment built around teamwork and trust, then consider furthering your career with us as a QUALITY SYSTEMS MANAGER ! Please read on

    Job Title: QUALITY SYSTEMS MANAGER

    SIGN-ON BONUS: $8,000 (30% at 6th month anniversary and 70% at 1st year anniversary)

    Summary:

    Evaluates processes, develops action plans, and coordinates the strategic implementation of system processes and corrective actions at the plasma donor center. Reports to the Regional Quality Manager.

    Primary Responsibilities for Role: Maintains oversight of the center's quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties. Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained. Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks. Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required. Continuously assesses, promotes, and improves the effectiveness of the quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations. Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Investigates identified trends and performs follow-up on corrective and preventive actions, system implementations, and process improvement plans to measure/determine effectiveness. Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment. Performs a review of the documentation of unsuitable test results and unit lookback information. Performs a review of donor adverse event reports and the applicable related documents. Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as may be required) is completed, documented, and on file. Performs employee training observations to ensure staff competency prior to releasing employees to work independently. Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-compliance. Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves deferred donor reinstatement activities. Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues. Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented. Holds monthly Quality Meeting to communicate status updates and manage action outcomes.
    Other Responsibilities for Role: Leads projects and initiatives as requested.
    This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.

    Job Requirements:

    EDUCATION: Bachelor of Science degree or equivalent. Certified and proficient in quality and compliance. EXPERIENCE: Typically requires 2-5 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood. EQUIVALENCY:

    Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

    KNOWLEDGE, SKILLS & ABILITIES:

    Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.

    Occupational Demands:

    Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32 , miscellaneous production Chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.

    "We are looking to grow our teams with people who share our energy and enthusiasm for creating the best experience for our donors/customers."

    Third Party Agency and Recruiter Notice:

    Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

    EEO:

    Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

    Location: NORTH AMERICA : USA : SD-Brookings

    Center Address: nd Ave South, Brookings, SD 57006

    Contact: Alex S. Contreras, Senior Talent Acquisition Partner -

    Learn more about Grifols Follow us on . click apply for full job details Read Less
  • G

    Quality Manager for Plasma Center  

    - Oldham
    table.MiTabla max-width: 1020px;!important Would you like to join an... Read More
    table.MiTabla max-width: 1020px;!important
    Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

    We're Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit!

    If you enjoy working in an environment built around teamwork and trust, then consider furthering your career with us as a QUALITY SYSTEMS MANAGER ! Please read on

    Job Title: QUALITY SYSTEMS MANAGER

    SIGN-ON BONUS: $8,000 (30% at 6th month anniversary and 70% at 1st year anniversary)

    Summary:

    Evaluates processes, develops action plans, and coordinates the strategic implementation of system processes and corrective actions at the plasma donor center. Reports to the Regional Quality Manager.

    Primary Responsibilities for Role: Maintains oversight of the center's quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties. Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained. Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks. Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required. Continuously assesses, promotes, and improves the effectiveness of the quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations. Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Investigates identified trends and performs follow-up on corrective and preventive actions, system implementations, and process improvement plans to measure/determine effectiveness. Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment. Performs a review of the documentation of unsuitable test results and unit lookback information. Performs a review of donor adverse event reports and the applicable related documents. Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as may be required) is completed, documented, and on file. Performs employee training observations to ensure staff competency prior to releasing employees to work independently. Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-compliance. Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves deferred donor reinstatement activities. Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues. Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented. Holds monthly Quality Meeting to communicate status updates and manage action outcomes.
    Other Responsibilities for Role: Leads projects and initiatives as requested.
    This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.

    Job Requirements:

    EDUCATION: Bachelor of Science degree or equivalent. Certified and proficient in quality and compliance. EXPERIENCE: Typically requires 2-5 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood. EQUIVALENCY:

    Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

    KNOWLEDGE, SKILLS & ABILITIES:

    Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.

    Occupational Demands:

    Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32 , miscellaneous production Chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.

    "We are looking to grow our teams with people who share our energy and enthusiasm for creating the best experience for our donors/customers."

    Third Party Agency and Recruiter Notice:

    Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

    EEO:

    Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

    Location: NORTH AMERICA : USA : SD-Brookings

    Center Address: nd Ave South, Brookings, SD 57006

    Contact: Alex S. Contreras, Senior Talent Acquisition Partner -

    Learn more about Grifols Follow us on . click apply for full job details Read Less
  • G

    Quality Manager for Plasma Center  

    - Volga
    table.MiTabla max-width: 1020px;!important Would you like to join an... Read More
    table.MiTabla max-width: 1020px;!important
    Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

    We're Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit!

    If you enjoy working in an environment built around teamwork and trust, then consider furthering your career with us as a QUALITY SYSTEMS MANAGER ! Please read on

    Job Title: QUALITY SYSTEMS MANAGER

    SIGN-ON BONUS: $8,000 (30% at 6th month anniversary and 70% at 1st year anniversary)

    Summary:

    Evaluates processes, develops action plans, and coordinates the strategic implementation of system processes and corrective actions at the plasma donor center. Reports to the Regional Quality Manager.

    Primary Responsibilities for Role: Maintains oversight of the center's quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties. Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained. Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks. Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required. Continuously assesses, promotes, and improves the effectiveness of the quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations. Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Investigates identified trends and performs follow-up on corrective and preventive actions, system implementations, and process improvement plans to measure/determine effectiveness. Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment. Performs a review of the documentation of unsuitable test results and unit lookback information. Performs a review of donor adverse event reports and the applicable related documents. Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as may be required) is completed, documented, and on file. Performs employee training observations to ensure staff competency prior to releasing employees to work independently. Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-compliance. Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves deferred donor reinstatement activities. Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues. Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented. Holds monthly Quality Meeting to communicate status updates and manage action outcomes.
    Other Responsibilities for Role: Leads projects and initiatives as requested.
    This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.

    Job Requirements:

    EDUCATION: Bachelor of Science degree or equivalent. Certified and proficient in quality and compliance. EXPERIENCE: Typically requires 2-5 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood. EQUIVALENCY:

    Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

    KNOWLEDGE, SKILLS & ABILITIES:

    Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.

    Occupational Demands:

    Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32 , miscellaneous production Chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.

    "We are looking to grow our teams with people who share our energy and enthusiasm for creating the best experience for our donors/customers."

    Third Party Agency and Recruiter Notice:

    Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

    EEO:

    Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

    Location: NORTH AMERICA : USA : SD-Brookings

    Center Address: nd Ave South, Brookings, SD 57006

    Contact: Alex S. Contreras, Senior Talent Acquisition Partner -

    Learn more about Grifols Follow us on . click apply for full job details Read Less
  • G

    Quality Manager for Plasma Center  

    - Bruce
    table.MiTabla max-width: 1020px;!important Would you like to join an... Read More
    table.MiTabla max-width: 1020px;!important
    Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

    We're Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 100 countries, have an unmatched record of product quality and safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit!

    If you enjoy working in an environment built around teamwork and trust, then consider furthering your career with us as a QUALITY SYSTEMS MANAGER ! Please read on

    Job Title: QUALITY SYSTEMS MANAGER

    SIGN-ON BONUS: $8,000 (30% at 6th month anniversary and 70% at 1st year anniversary)

    Summary:

    Evaluates processes, develops action plans, and coordinates the strategic implementation of system processes and corrective actions at the plasma donor center. Reports to the Regional Quality Manager.

    Primary Responsibilities for Role: Maintains oversight of the center's quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties. Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance. Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained. Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks. Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required. Continuously assesses, promotes, and improves the effectiveness of the quality and training systems in the donor center through recognition of trends, investigation of failures in the execution of procedures, and direct observations. Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. Investigates identified trends and performs follow-up on corrective and preventive actions, system implementations, and process improvement plans to measure/determine effectiveness. Oversees product and biohazard waste shipments: Ensures shipments meet regulatory specifications and product release requirements; ensures accurate labeling and documentation; and, authorizes final shipment. Performs a review of the documentation of unsuitable test results and unit lookback information. Performs a review of donor adverse event reports and the applicable related documents. Ensures that job and center annual training (i.e. Advanced cGMP, Blood Borne Pathogen, and others as may be required) is completed, documented, and on file. Performs employee training observations to ensure staff competency prior to releasing employees to work independently. Ensures that all supplies and materials ordered meet quality requirements prior to use and are always stored in appropriate temperature/facility conditions. Initiates appropriate investigations if these requirements are not met. Initiates rejection of supplies for non-compliance. Determines donor suitability activities and manages donor deferrals as appropriate. Reviews and approves deferred donor reinstatement activities. Prepares quality analysis reports to track issues and set goals. Does in depth research and analysis to resolve systemic compliance issues. Ensures that Clinical Laboratory Improvement Amendments (CLIA) proficiency test surveys, complaint investigations, and training have been properly documented. Holds monthly Quality Meeting to communicate status updates and manage action outcomes.
    Other Responsibilities for Role: Leads projects and initiatives as requested.
    This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.

    Job Requirements:

    EDUCATION: Bachelor of Science degree or equivalent. Certified and proficient in quality and compliance. EXPERIENCE: Typically requires 2-5 years of related experience in a medical and/or cGMP regulated environment. Experience with plasma or whole blood. EQUIVALENCY:

    Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

    KNOWLEDGE, SKILLS & ABILITIES:

    Command of interpersonal communication, organizational and problem-solving abilities. Ability to understand and assess FDA regulations. Strong integrity and commitment to quality and compliance. Full command of mathematics. Legible handwriting. High level of proficiency with computers. Proficient in root cause analysis and corrective/preventative actions. Ability to balance multiple competing priorities. Strong time management abilities. Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team. Ability to work with minimal supervision. Ability to travel when needed for meetings, events, and occasional support of other centers.

    Occupational Demands:

    Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32 , miscellaneous production Chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.

    "We are looking to grow our teams with people who share our energy and enthusiasm for creating the best experience for our donors/customers."

    Third Party Agency and Recruiter Notice:

    Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

    EEO:

    Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

    Location: NORTH AMERICA : USA : SD-Brookings

    Center Address: nd Ave South, Brookings, SD 57006

    Contact: Alex S. Contreras, Senior Talent Acquisition Partner -

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