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Joulé
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  • Material Handler I  

    - Rockville
    Job Title: Material Handler I Location: Rockville, MD Duration: 12-mon... Read More
    Job Title: Material Handler I Location: Rockville, MD Duration: 12-month contract Pay Rate: $20-$27/hr Overview: The Material Handler I will support warehouse operations by managing the receipt, inspection, and movement of materials used in GMP manufacturing. This individual will ensure compliance with all internal procedures and applicable regulations, maintain accurate inventory control, and collaborate with cross-functional teams to ensure timely material flow to manufacturing. Responsibilities: Receive, inspect, and disposition incoming materials to ensure compliance with company, GMP, and regulatory requirements. Ensure accurate inventory control of all controlled materials and execute required cycle counts and inventory reconciliations. Execute material flow and warehouse operations in accordance with SOPs, GMP, FDA, OSHA, IATA, DOT, TSA, and other applicable regulations. Coordinate with Quality Control and Quality Assurance to ensure sampling and release of materials for GMP manufacturing. Operate warehouse equipment, including forklifts and pallet jacks, in a safe manner compliant with OSHA standards. Support shipping, receiving, labeling, and storage of materials as required. Requirements: High School Diploma or equivalent required. Previous experience in materials management, warehousing, or logistics within the biotech or pharmaceutical industry. Working knowledge of GMP, FDA, and OSHA regulations. Ability to operate forklifts and pallet jacks safely; forklift certification preferred. Strong attention to detail, organizational skills, and ability to work in a fast-paced, regulated environment. Ref: Read Less
  • (Cosmetics/Skincare Focused) Resident Sales Associate (Temp)  

    - Jersey City
    Job Title: Resident Sales Associate (Temp) Location: Jersey City, New... Read More
    Job Title: Resident Sales Associate (Temp) Location: Jersey City, New Jersey Type: Contract To Hire Compensation: $27 - $27 hourly + commission Company Overview: Our company is a recognized global leader in medical biotechnologies, specializing in cellular therapies. We are seeking talented and competitive Inside Sales professionals who thrive in a sales and manufacturing-driven environment. Responsibilities: Conduct outreach to skincare clinics, med-spas, and dermatology offices to present product lines and build relationships. Follow up on prospective and existing clients, documenting all outreach in CRM (Salesforce). Deliver strong customer service and product education, explaining features and benefits of topical skincare and PRP-based products. Identify cross-sell and upsell opportunities within existing accounts. Manage inbound inquiries and resolve product or order issues. Collaborate with marketing and customer support teams to ensure a positive client experience. Maintain consistent sales activity and meet weekly outreach metrics. Participate in ongoing product knowledge and sales development sessions Requirements: Bachelor's degree in Biology or related field strongly preferred. 1-2 years of inside sales experience, ideally in skincare, cosmetics, or aesthetic product sales. 1+ years' experience with CRM. Strong phone presence with high call activity. Excellent verbal/written communication and organizational skills. Ability to multi-task, prioritize, and manage time effectively. Local to Jersey City, NJ. Must be in-office daily. Must not have previously interviewed with the company. Read Less
  • OMICS Laboratory Research Technician IV  

    - Pittsburgh
    Title: OMICS Laboratory Research Technician IV Location: Onsite, Pitts... Read More
    Title: OMICS Laboratory Research Technician IV Location: Onsite, Pittsburgh, PA 15219 Type: 6-month contract to hire Hours: 8AM-5PM Start: December Overview: Join a vital institutional core research team to support biological research by using techniques from various fields like genomics, proteomics, and transcriptomics. Also, analyzes and interprets data, compiles results, and prepares reports. Maintains inventory, ordering, and logs. Writes manuscripts and grant proposals and prepares data visualizations. If you're passionate about advancing research through independent and complex laboratory work, apply today! Responsibilities Perform a variety of independent and complex laboratory experiments, including determining experimental protocols, preparing laboratory specimens, and maintaining cell cultures in compliance with established SOPs. Independently perform clinical and research testing following CLIA/CAP and institutional standards. Process clinical, QC, and PT specimens through established workflows while demonstrating strong analytical and problem-solving skills. Accurately record and maintain all experimental and clinical data, ensuring completeness in logbooks, laboratory notebooks, and Laboratory Information Management Systems (LIMS). Utilize barcode scanning to verify chain-of-custody and track sample progression through multiple workflows. Maintain proficiency in molecular biology and genomic techniques, including but not limited to: Nucleic acid extraction and quantitation PCR, RT-PCR, and qPCR Sanger sequencing, methylation analysis, LOH, and MassARRAY MALDI-TOF Next-Generation Sequencing (NGS) Operate, calibrate, and perform routine maintenance on laboratory instrumentation. Troubleshoot issues related to instruments, methodology, or specimens and implement corrective actions per established protocols. Perform high-volume sample triage and accessioning of various sample types (blood, plasma, urine, saliva, swabs, stool, tissue-derived materials) following CAP/CLIA SOPs, ensuring accurate labeling, barcoding, and traceability within LIMS. Analyze experimental and clinical data, interpret results, and compile findings into detailed reports, charts, and summaries for internal and publication use. Contribute to manuscript preparation, grant proposals, and literature reviews, summarizing data to support research and regulatory documentation. Develop and recommend improvements to laboratory operations, methodologies, and workflows to enhance research efficiency and quality. Serve as Safety Officer or equivalent as needed, ensuring adherence to all laboratory safety, biosafety, and compliance regulations. Participate in continuing education, seminars, and internal development programs to maintain and expand professional and technical expertise. Effectively communicate with team members and leadership to ensure smooth daily operations and consistent quality outcomes. Requirements Bachelor'sdegree 3+ years of relevant experience Proficiency in molecular biology and genomic techniques, including but not limited to: Nucleic acid extraction and quantitation sample preparation PCR, RT-PCR, and qPCR Next-Generation Sequencing (NGS) Advanced Excel skills Strong organizational skills, attention to detail, problem-solving abilities, and the capacity to work both independently and as part of a collaborative team System One, and its subsidiaries, including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: Read Less
  • OMICS Laboratory Lead/Manager II  

    - Pittsburgh
    Title: OMICS Laboratory Manager II Location: Onsite, Pittsburgh, PA 15... Read More
    Title: OMICS Laboratory Manager II Location: Onsite, Pittsburgh, PA 15219 Type: 6-month contract to hire Hours: 8AM-5PM Start: December Overview: Join as a Laboratory Manager II to monitor personnel and workflow in the area. Track and monitor QA/QC in conjunction with other laboratory leadership. Oversee laboratory throughput metrics and workflow optimization, ensuring balanced workloads, adherence to deadlines, and high data fidelity under time-sensitive conditions. Responsibilities Manages daily laboratory operations of a division, department, function, or program, including conducting and overseeing quality assurance and quality control. Perform clinical testing in accordance with established SOPs. Maintain oversight of all clinical testing. Maintain clinical workflow for area to meet established quality and TAT, including technologist and bench schedule, status of cases (STAT, special request, etc). Maintain competency for all benches in area. Rotate regularly through clinical workflow. Be able to step in and help clinical work when necessary. Troubleshoot problematic cases, including when to repeat case and when to cancel testing. Act as point-person for communication with vendors regarding problems with instruments and/or software. Update SOPs, as needed, to maintain current accurate procedure documentation. With support and guidance from laboratory leadership and Medical Director, oversee supplemental validations and implementation of procedural changes. Write-up all supplemental validations and compile supporting data. Oversee training of technologists, including new hires and cross training of current technologists. Monitor and assess competency for all area technologists. Adhere to CAP and other regulatory agency regulations for competency assessment. Monitor Proficiency Testing for assays in area. Track all results for concordance and document as appropriate. Work with MGP QA and lab leadership and Medical Director as needed for preparation for inspections. Complete performance reviews for all area Molecular Genomic Specialists. Monitor and approve reagent/supply orders for area. Act as liaison for daily happenings in clinical workflow between technologists and laboratory leadership. Track area technologist indirect hours (MRS). Work with laboratory leadership including Medical Director for ideas for, validation of and implementation of development projects. Maintain track of technical and professional development, including but not limited to attendance at seminars/webinars and participation in educational programs and activities. Oversee sample triage, barcoding, and data integrity across all omics workflows. Ensure consistent application of CAP/CLIA-compliant procedures for sample tracking, storage, and LIMS documentation across genomic, proteomic, metabolomic, and lipidomic assays. Coordinate operation, scheduling, and maintenance of high-throughput automation platforms (Eppendorf, Tecan, Hamilton) and analytical instruments (Orbitrap Exploris, Stellar, SomaLogic, iScan). Provide mentorship and cross-training on multi-omics sample preparation, instrument workflows, and data tracking protocols to ensure consistency and scalability across teams. Lead validation and process harmonization for new assays across omics platforms. Collaborate with QA and regulatory teams to maintain CAP/CLIA readiness and audit documentation. Requirements Bachelor's degree required Minimum of 3 years of relevant experience in a high-volume, complex clinical or research laboratory setting Advanced Excel skills Proficient in molecular biology techniques, including Illumina NGS Next-Generation Sequencing, PCR, library preparation, and barcoding Troubleshooting, mentoring and QC review experience Experience with laboratory automation and robotic systems, such as Hamilton instruments and automated liquid handlers System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: Read Less
  • OMICS Laboratory Manager I  

    - Pittsburgh
    Title: OMICS Laboratory Manager I Location: Onsite, Pittsburgh, PA 152... Read More
    Title: OMICS Laboratory Manager I Location: Onsite, Pittsburgh, PA 15219 Type: 6-month contract to hire Hours: 8AM-5PM Start: December Overview: Join as a Laboratory Manager I to manage day-to-day laboratory operations while ensuring compliance with safety regulations and best practices. Works with, adapts, and installs scientific equipment in research laboratories. Collaborates on routine projects and procedures. Manages inventory and equipment and performs budget functions Responsibilities Manages daily laboratory operations of a division, department, function, or program, including conducting and overseeing quality assurance and quality control. Maintains and adapts scientific equipment for experimental needs of the department. Troubleshoots, installs, and adapts electronic devices and other samples for research investigations. Confers with researchers and faculty concerning research needs and methods. Prepares budget requests and manages approved budget. Keeps accurate and timely data logbooks. May perform duties of lower-level roles e.g. Laboratory Research Technician, Research Program Coordinator, etc. Ensures compliance with all applicable regulations for waste disposal; acts as department safety officer Requirements Bachelor's degree required Minimum of 3 years of relevant experience in a high-volume, complex clinical or research laboratory setting Advanced Excel skills Proficient in molecular biology techniques, including Illumina NGS Next-Generation Sequencing, PCR, library preparation, and barcoding Experience with laboratory automation and robotic systems, such as Hamilton instruments and automated liquid handlers System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. LI-MD1 Ref: Read Less
  • Chemistry Laboratory Technician  

    - Bridgewater
    Job Title: Chemistry Laboratory Technician Location: Bridgewater, NJ H... Read More
    Job Title: Chemistry Laboratory Technician Location: Bridgewater, NJ Hours/Schedule: Monday-Friday, 8 am to 5 pm Compensation: $30.00 - $35.00/hr Type: Contract, Potential for extension or conversion to permanent Overview This role supports laboratory testing and formulation work for chemistry-based adhesive products. The position conducts testing, documentation, and compliance activities to ensure product quality and adherence to safety and regulatory requirements. It works independently and collaboratively with internal partners to deliver accurate test data and support ongoing development work. Responsibilities Handle and test multiple chemistry-based adhesive products Develop and execute test plans for formulations Perform tests independently according to product requirements Conduct gauge R&R on lab-produced batches Generate test data, documentation, and reports Ensure laboratory safety, hygiene, and compliance with SHE standards Communicate results and needs with internal teams Lift materials and operate equipment required for laboratory procedures Qualifications Bachelor's degree in Chemistry or Materials Science with 3+ years of experience in rubber, plastics compounding, or coatings; or Associate's degree in Chemistry or Materials Science with 5+ years of related industry experience; or Equivalent combination of education and experience in rubber, plastics compounding, or coatings Experience performing laboratory tests and generating technical documentation Ability to work independently and follow established testing protocols Familiarity with SHE/lab safety practices Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan. Ref: Read Less
  • Animal Research Technician  

    - Athens
    Job Title: Animal Care Technician Location: Athens, GA Hours/Schedule:... Read More
    Job Title: Animal Care Technician Location: Athens, GA Hours/Schedule: M-F, 8-4:30 Type: Contract Job Overview The Animal Care Technician is responsible for providing animal husbandry, health care, and research support in compliance with federal regulations, study protocols, and accreditation standards. This role involves daily animal care, health monitoring, sample collection, equipment and facility maintenance, and assisting with scientific procedures under Biosafety Level 1 and 2 conditions. The technician may also provide guidance to junior staff and support site-level committees or workgroups. Responsibilities Perform daily animal husbandry including feeding, watering, enrichment, and facility sanitation. Monitor animal health and welfare, recognize abnormal conditions, and report to the Site Veterinarian or Group/Team Leader. Restrain animals for routine and emergency procedures; administer treatments under veterinary direction. Conduct scientific observations, disease assessments, and record study data per protocol. Assist with clinical R&D sample collection (blood, feces, swabs, tissues) and necropsy procedures. Support experimental treatment administration and, under supervision, sedation monitoring or euthanasia. Maintain, adjust, and repair pens, feeders, drinking systems, and handling equipment. Perform biosecurity tasks such as water sanitation, feed/fomite decontamination, and environmental sampling. Document and maintain records for animal care, preventive medicine, USDA compliance, and study protocols. Provide guidance to junior team members and participate in site-specific committees or workgroups. Qualifications High School Diploma or GED required; additional training in animal science, veterinary technology, or related field preferred. Experience working with livestock or laboratory animals preferred. Ability to lift up to 70 lbs occasionally and 50 lbs frequently; capable of working in hot, cold, noisy, or humid environments. Willingness to work directly with animals during ante-mortem and post-mortem procedures. Must not have allergies to animals or livestock/feed dust. Ability to comply with biosafety requirements and maintain accurate documentation. Benefits System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan. Ref: Read Less
  • Ingredient Compliance Specialist  

    - Parsippany
    Job Title: Ingredient Compliance Specialist Type: Direct Hire Location... Read More
    Job Title: Ingredient Compliance Specialist Type: Direct Hire Location: Morris County, NJ (Whippany/Parsippany, NJ) Schedule: Hybrid 9:00 a.m.-5:00 p.m. Salary: $70,000-$85,000 + performance bonus About the Opportunity We are seeking an Ingredient Compliance Specialist to join our Qualityto. This role is ideal for professionals with experience in food, beverage, functional ingredients, nutraceuticals, dietary supplements, or contract manufacturingb/ co-packing environments. You will play a key role in ensuring quality and regulatory compliance across raw materials and finished goods, working closely with suppliers, co-packers, CMOs, and internal teams. This position supports a diverse portfolio of food, beverage, ingredient, and dietary / nutritional products, combining technical expertise with practical problem-solving in a fast-paced supply chain setting. What We're Looking For Experience with Contract Manufacturing Organizations (CMOs), co-packers, or ingredient suppliers in food, beverage, supplement, or nutraceutical industries. Proven expertise in company and supplier quality management and product approvals. Preventive Controls Qualified Individual (PCQI) Certification (or willingness to obtain). 3-5 years of Quality Assurance (QA) experience in food, beverage, ingredients, dietary supplements, or nutraceutical manufacturing. Strong understanding of U.S. Food and Drug Administration (FDA) regulations, dietary ingredient and beverage requirements, Hazard Analysis Critical Control Point (HACCP), Hazard Analysis and Risk-Based Preventive Controls (HARPC), and general quality compliance standards. Working knowledge of Food Safety Modernization Act (FSMA), including Foreign Supplier Verification Program (FSVP) / Foreign Supplier Verification Activities (FSVA). Technical documentation expertise: Safety Data Sheets (SDS), specifications, allergen/GMO statements, BSE/TSE letters, nutritional data, test methods, certifications, and Supplier Ingredient Data Information (SIDIs). Proficiency in Microsoft Excel, Word, and Outlook, and experience with Customer Relationship Management (CRM) or Quality Management Systems (QMS) (Salesforce, ComplianceQuest preferred). Key Responsibilities Review and assess supplier-provided technical documents, including specifications, SDSs, flow charts, allergen/GMO statements, BSE/TSE letters, nutritional data, test methods, certifications, and SIDIs. Lead product and supplier approval processes, ensuring compliance with internal SOPs, regulatory standards, and customer expectations. Partner with co-packers, CMOs, and ingredient suppliers to gather updated documentation and evaluate change notifications. Manage change control workflows, ensuring timely and accurate communication across internal and external stakeholders. Respond to customer documentation requests related to ingredients, products, beverages, and manufacturing facilities. Confirm alignment between customer and supplier specifications for product approvals, orders, and custom requests. Oversee product release, ensuring all items meet testing, documentation, and quality standards before distribution. Maintain and upload current technical data and quality documentation in ComplianceQuest. Support sample management processes, including storage, tracking, and outgoing shipments with proper documentation. Perform additional duties as assigned by Quality leadership (Associate Director or Vice President of Quality). System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: Read Less
  • Social Media Intern  

    - Edison
    Job Title: Social Media Intern Location: Edison, NJ Type: Contract Com... Read More
    Job Title: Social Media Intern Location: Edison, NJ Type: Contract Compensation: $18.00 hourly Contractor Work Model: Hybrid - 3 days onsite, 2 days remote Hours: 8-5 M-F POSITION SUMMARY: As a Social Media Intern at Joule, you will gain practical experience in developing and executing marketing strategies with a strong emphasis on video content creation. Working closely with our Brand Awareness Manager and VP of Recruitment, you will contribute to content creation, manage the social media calendar, and engage with the Joule community across various platforms. ESSENTIAL FUNCTIONS: Under the guidance and support of a marketing team, the responsibilities listed below highlight the key tasks you will undertake during specific timeframes, which will be established throughout the training and development period. Content Creation (Video Focus): Develop engaging video content for various platforms (LinkedIn, Facebook, Instagram, Twitter, TikTok, and others). Assist in planning and producing video shoots, including storyboarding, filming, and editing. Create other content formats such as blog posts, infographics, and social media graphics. Social Media Management: Assist in planning and developing social media campaigns. Schedule, post, and execute content across multiple social media platforms. Engage with the audience on all social media channels. Monitor social media channels for trending topics and opportunities. Marketing Campaign Support: Contribute to the development and execution of candidate and client outreach campaigns. Brainstorm digital marketing and campaign ideas. Performance Analysis and Reporting: Track user engagement and performance on various social media platforms. Assist in analyzing analytics on a weekly/monthly basis. SECONDARY FUNCTIONS: Stay up-to-date on social media trends and emerging platforms. Participate in marketing team meetings and brainstorming sessions. Perform other duties as assigned. EDUCATION, EXPERIENCE, and SKILLS REQUIRED EDUCATION Currently pursuing a BS in Business, Marketing, Communications, or related field. EXPERIENCE No prior professional experience required; relevant coursework, extracurricular activities, or personal projects (especially in video creation) are a plus. Demonstrated interest in social media marketing and content creation. SKILLS REQUIRED Proficiency with social media platforms (LinkedIn, Instagram, Facebook, Twitter, TikTok, etc.). Basic video editing skills Strong written and verbal communication skills. Creative thinking and a passion for content creation. Ability to work independently and as part of a team. Basic understanding of social media analytics. Familiarity with graphic design tools (Canva or similar) is a plus. CORE VALUES Teamwork Coachability Results-Oriented Communication Ownership Reliability System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: Read Less
  • Temporary Senior Corporate Counsel, Contracts Attorney  

    - Alameda
    Job Title: Senior Corporate Counsel, Contracts Attorney Location: Alam... Read More
    Job Title: Senior Corporate Counsel, Contracts Attorney Location: Alameda, CA (100% Onsite - Remote candidates will not be considered) Hours/Schedule: Contract Compensation: $115-$135/hour doe Type: Contract Overview A leading biotechnology company located in Alameda, California is seeking a Senior Corporate Counsel, Contracts Attorney to support its growing Legal team. This role plays a key part in advancing R&D operations through expert contract drafting, negotiation, and risk management. Candidates must work onsite daily; remote work is not available. If you're ready to bring your legal expertise to a fast-paced biotech environment, apply today for immediate consideration. Responsibilities Draft, review, and negotiate a wide range of R&D, manufacturing, licensing, and supply agreements. Serve as the primary legal contact for R&D-related contracts and vendor agreements. Provide practical, business-focused legal advice and risk assessments to internal stakeholders. Collaborate across departments to ensure contracts align with operational goals and compliance standards. Maintain and update standard agreement templates and support continuous process improvement. Oversee and guide junior attorneys or contract managers during review and negotiation processes. Requirements J.D. and active U.S. bar membership required. 5+ years of transactional legal experience, ideally in biotech or pharmaceutical R&D environments. Proven ability to draft and negotiate complex agreements independently and efficiently. Strong written, verbal, and interpersonal communication skills with attention to detail. Proficiency in Microsoft Office, document management systems, and redlining tools. Highly organized, adaptable, and able to manage multiple priorities under tight deadlines. System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: Read Less

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