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Nutramax Laboratories
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  • Nutramax desires to provide a drug-free, healthful, and safe workplace... Read More
    Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check and drug screen (subject to applicable law). This position is 100% on site, Monday through Friday - 8:30am - 5pm, and you may be required to work in any SC location based on need. Summary of the Position: Lead all warehouse and distribution functions across multiple sites with multiple shifts. This leadership role requires both customer-facing and manufacturing-facing interaction. Essential skill requirements include: Strong, positive people skills Analytical, hands-on problem solving ERP systems and spreadsheet capabilities Cross-functional team building experience Ideal candidate will have experience dealing with distributors, brick and mortar retailers, and ecommerce customers, particularly Amazon. This role requires a quick learner capable of growing along with the organization. This position will work with operations, marketing/business teams, finance, and other functional partners to deliver the desired product to the intended customer in a timely, cost-efficient manner. Roles and Responsibilities: Lead all warehouse and distribution processes in a safe, professional, quality-focused, efficient manner while adhering to the company's Leadership Model Maintain accurate inventory levels for all materials Partner with Distribution and Warehouse managers to negotiate and bid freight rates for inbound and outbound freight Drive productivity, quality, and efficiency improvements Assure product arrives at customer on time Develop measurable goals that support corporate strategies and objectives Review/recommend purchases and coordinate maintenance on all support equipment – forklifts and pallet jacks Deliver all materials on time to Manufacturing Move, store, and deliver all materials in a cGMP compliant manner Create, maintain, and revise all relevant SOPs Identify and communicate all potential obsolete inventory issues preventing costly material write-offs Develop facility and network designs insuring long-term success Perform other assigned duties as required in meeting company objectives Communicate effectively with other departments within the organization and function within a team environment. Regular attendance is required Minimum Requirements: Strong organizational and leadership skills with the ability to handle multiple projects. Must be able to work in a fast-paced environment. Strong written and verbal communication skills required. Must be computer literate. Must have proficient working knowledge of SAP; S4/HANA preferred. Education and Experience: A Bachelor's Degree in a business, engineering, or supply chain discipline with a minimum of seven years of supply chain management experience, preferably in a manufacturing environment. Read Less
  • Nutramax desires to provide a drug-free, healthful, and safe workplace... Read More
    Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check and drug screen (subject to applicable law). This position is 100% on site in our Lancaster, SC Headquarters (roughly 45 min - 1 hour south of Charlotte, NC). Position Summary: The Associate Director, Clinical Research will provide scientific support across Nutramax Laboratories Veterinary Sciences, Inc. research development and commercial programs. This position will report to the Director of Clinical Development and work with cross-functional multidisciplinary study teams on clinical trial strategy, design and execution and ensure Good Clinical Practices (GCPs) are followed. This individual will help develop protocols, review trial data, interact with external stakeholders, and participate/contribute scientific expertise for ongoing research focusing on all body systems for animal species. Responsibilities : Direct, plan and lead clinical research and develop timetables, budgets and resource analysis for clinical research and personnel administration. Participate in due diligence activities for potential business development opportunities from a research perspective. Design, implement and monitor clinical research to ensure timely completion of studies. Monitor and assist in reporting clinical trial data for safety and efficacy. Liaise with site investigators and study staff to ensure safety of subjects and compliance with the protocol. Partner with data management personnel to plan data entry and analysis and recruit, screen and select qualified investigators. Strong ability to organize and excellent presentation skills Ensures that Good Clinical Practices (GCPs) are followed. Responsible for writing clinical reports upon completion or termination of studies. Establish and maintain relationships with alliance partners, external companies, investigators and key opinion leaders to optimize performance on clinical trial activities. Lead team in the preparation of manuscripts for scientific and medical journals and prepare and present at scientific meetings. Work with project management to keep project plan current Work cross functionally with other departments on specific projects Perform other assigned duties as may be required in meeting company objectives Requirements : A PhD in Animal Sciences or Animal Nutrition, OR Doctor of Veterinary Medicine (DVM/VMD) with special interest in nutrition desired. A minimum of 5-8 years of relevant experience conducting clinical research. Ability to solve complex scientific problems and to work equally effectively as a leader with external partners, or as a member within a matrixed, team environment. Ability to work effectively and collaboratively with scientists on cross-functional projects teams, and comfortable to work at a fast-paced environment. Read Less
  • Quality Assurance Inspector I The hours for this position are Monday -... Read More
    Quality Assurance Inspector I The hours for this position are Monday - Thursday 3:15pm - 11:30pm and Friday 3:15pm - 10:15pm. Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check, drug screen (subject to applicable law) and reading comprehension test. Summary of the Position: The Quality Assurance Inspector I reports to Quality Assurance Management. This position is responsible for the daily Quality Assurance support in the Manufacturing and Packaging process on site. They will be required to review all appropriate documents during the production process. In this role, the Quality Assurance Inspector is required to maintain and have a consistent presence on the production floor during the shift and be readily available to support the production processes in their assigned areas. Roles and Responsibilities: Providing Quality Assurance presence in production areas through the daily execution of Product Packaging lines, Product Manufacturing Processes, room clearances and release of cleaned equipment/rooms/areas, and in-process inspections in all Nutramax manufacturing areas. Providing input for the revision process of SOPs to cover work requirements in the assigned facility or process. Assisting in the investigation of deviations Reviewing the pest control and environmental monitoring system Issuance of Labels and/or other printed material to operations as per current production schedule Assist with identification of minor and major errors and deficiencies found within batch records Organize work to achieve daily goals with no errors or deficiencies Providing impact on issues that could affect product quality, safety and purity Assisting Quality Assurance management with the daily operation of the QA Hold area Submitting thorough End of Day reports including detail summary of daily activities, issues and actions taken Must be able to effectively communicate with other departments and function within a team environment Training on all SOPs, safety procedures and cGMPs as required and must be current Regular attendance is required. Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives. Communicate effectively with your team, supervision and other departments within the organization and function within a team, promoting positive work environment This position will be closely associated and work with the following: Manufacturing and Packaging Operators Quality Associates (QA team lead, QA Management, QC, Label Issuance, Quality Assurance Document Specialist) Safety, Security and Environmental Services Departments Training Department Supply Chain Team Product Development Minimum Requirements: The Quality Assurance Inspector I must have two years' experience in the pharmaceutical, food, dietary supplement manufacturing environment or any other government regulated environment preferred. Auditing experience and troubleshooting is a plus. Great enthusiasm and hard work ethic is a must. Detail oriented and team centered approach is required. Good computer skills on all general software is needed Microsoft Office Suite. The ability to lift 50lbs. Must wear Personal Protective Equipment and follow all appropriate written and verbal instructions and procedures. Education and Experience: This position requires a High School Diploma or equivalent. Supervisory Responsibilities: None Read Less

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Astrid-Lindgren-Weg 12 38229 Salzgitter Germany