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  •  ...Job Posting Implement, control and coordinate changes in documentation. Facilitates the updating and routing of controlled documents, including, but not limited to, Governance and Procedure documents, Master Forms and Master Batch Records within the eDMS. Review documents... 
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    Katalyst HealthCares & Life Sciences

    Neshanic Station, NJ
    1 day ago
  •  ...Documentation Manager The mission for this position is to manage internal and external documentation requests and updates. These include but are not limited to policies, procedures, specification review and data analysis, customer complaints, and customer documentation... 
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    All shifts
    Monday to Friday

    Stahlbush Island Farms

    Corvallis, OR
    3 days ago
  •  ...Job Description: Implement, control and coordinate changes in documentation. Facilitates the updating and routing of controlled documents, including, but not limited to, Governance and Procedure documents, Master Forms and Master Batch Records within the eDMS.... 
    Suggested

    Katalyst Healthcares and Life Sciences

    Neshanic Station, NJ
    4 days ago
  • $23 per hour

    A staffing company is seeking a Bilingual Documentation Specialist to support Quality Assurance in a laboratory environment. Responsibilities include maintaining accurate documentation, managing stability programs, and ensuring compliance with cGLP/GMP regulations. The... 
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    Hourly pay
    Monday to Friday

    5TH HQ

    Florida, NY
    21 hours ago
  • A healthcare services provider is seeking a QA Specialist in Jacksonville, Florida. This role emphasizes the review and improvement of documentation and operational outputs, ensuring compliance with quality standards. The ideal candidate will have a certification in a... 
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    Wellbox Health

    Jacksonville, FL
    21 hours ago
  • A dynamic telecommunications company based in Tampa is seeking a QA & Documentation Specialist. This role is pivotal in ensuring reliable feature releases, documenting processes clearly, and providing resources for users. Ideal candidates should possess 1-3 years in software... 
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    TeleVoIPs, LLC

    Tampa, FL
    4 days ago
  • A well-known health supplement company seeks a Documentation Specialist in El Segundo, CA, for a 3-month hybrid contract covering maternity leave...  ...ERP systems. Ideal candidates should have at least 2 years of QA experience and a relevant bachelor's degree. #J-18808-Ljbffr... 
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    Contract work

    Vaco

    Los Angeles, CA
    2 days ago
  • Job Description The QA Engineer is responsible for ensuring timely development, review, and approval of engineering, validation, and lifecycle documentation in alignment with corporate procedures, SOPs, cGMP, and industry best practices. This role supports manufacturing... 
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    Katalyst CRO

    Tampa, FL
    3 days ago
  • $20 - $25 per hour

    JOB TITLE: QA & Documentation Specialist LOCATION: Tampa, FL EMPLOYMENT TYPE: Full-time STATUS: Non-Exempt HOURS: 40 hours per week; Monday - Friday, 8:00AM - 5:00PM COMPENSATION: $20/hr - $25/hr (Based on experience) ABOUT US: TeleVoIPs is a rapidly growing cloud-based... 
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    Full time
    Local area
    Monday to Friday

    TeleVoIPs, LLC

    Tampa, FL
    4 days ago
  • A leading company in dietary supplements is looking for a Documentation Specialist for a 3-month contract role. This hybrid position requires support...  ...The ideal candidate will have over 2 years of experience in QA within the food or dietary supplement industry and possess... 
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    Contract work

    Vaco by Highspring

    El Segundo, CA
    2 days ago
  • A leading company in food and beverage is seeking a Documentation Specialist for a 3-month contract to support their Quality Assurance team. The...  ...Tuesdays and Thursdays. Ideal candidates will have 2+ years of QA/Regulatory experience and a Bachelor's degree in a related... 
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    Contract work

    Vaco Recruiter Services

    Los Angeles, CA
    2 days ago
  •  ...is seeking dedicated individuals to join their Material Review Board team in Indianapolis. This role is focused on reviewing and documenting Non-Conformances, ensuring all records are accurate and comply with company standards. Ideal candidates will possess strong communication... 
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    Day shift

    TechDigital Group

    Indianapolis, IN
    21 hours ago
  • $22.6 - $38 per hour

    A pharmaceutical company in Bedford, Ohio is seeking a Document Associate to manage document control for the manufacturing site. Responsibilities include creating and filing GMP documentation, authoring SOPs, and liaising with various functional groups. The ideal candidate... 
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    Hourly pay

    Hikma Pharmaceuticals

    Bedford, OH
    2 days ago
  • $22 - $24 per hour

     ...QA/QC Documentation Specialist We are seeking a meticulous and dedicated QA/QC Documentation Specialist to join our team. The successful candidate will ensure compliance with regulations and internal quality control practices, with a focus on document review, verification... 
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    Temporary work
    Work at office
    Immediate start
    Monday to Friday

    Actalent

    Grove City, OH
    29 days ago
  • $38.41 - $41.55 per hour

    A pharmaceutical company located in New York seeks a Quality Compliance Reviewer to ensure quality standards for laboratory data. Candidates should possess a Bachelor's degree in the Physical Sciences or Mathematics, and have at least 2 years of experience in a laboratory...
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    Hourly pay

    American Regent, Inc.

    Shirley, NY
    1 day ago
  • $28.98 per hour

     ...provisional reduction/avoidance plan, among other critical functions. Position Responsibilities We are seeking a Training QA & Documentation Specialist to join the eLearning team within the Bureau of Workforce Operations. This role ensures that all online training content... 
    Work at office

    City of New York

    New York, NY
    4 days ago
  • A leading contract research organization in Tampa is seeking a QA Engineer to ensure compliance with quality standards and regulatory...  .... The ideal candidate will review and approve validation documents, support the validation lifecycle, and help maintain inspection... 
    Contract work

    Katalyst CRO

    Tampa, FL
    3 days ago
  •  ...Responsibilities include creating and verifying product labels, maintaining inventory levels, and ensuring compliance with customer documentation. Candidates should possess strong attention to detail, critical thinking skills, and the ability to multi-task. The position... 

    Knowles Precision Devices

    Cazenovia, NY
    21 hours ago
  • A manufacturing company in the Town of Cazenovia, NY is seeking a Closing Desk Operator. This role involves supporting the Quality Assurance Department's operations, including labeling, packaging, and scanning records. Strong attention to detail and basic skills in Microsoft...
    Work at office

    Knowles Corporation

    Cazenovia, NY
    2 days ago
  •  ...Role Summary Supports quality assurance, documentation development, business-rule reviews, and standardization of processes for national...  ...Procedures (SOPs) and detailed desktop procedures. Conduct QA reviews of data-collection products, reports, methodologies, and... 

    Silo Smashers

    Clarksburg, WV
    2 days ago
  •  ...Our client, a leader in the food and beverage industry, is seeking a QA Document Control Specialist to join their team. As a QA Document Control Specialist, you will be part of the Quality Assurance department supporting documentation management and compliance efforts... 
    Weekly pay
    Temporary work
    Work experience placement
    Flexible hours

    Experis/Manpower Group

    Upper Deerfield, NJ
    4 days ago
  • $72k - $90k

     ...QA Document Control Specialist Location: On-site (Connecticut) Schedule: Full-Time Salary Range: $72,000 - $90,000/year (based on experience) Position Overview The QA Document Control Specialist will play a key role in maintaining... 
    Full time

    Affinity Executive Search

    Vernon, CT
    2 days ago
  •  ...Responsibilities: Manage and maintain paper-based controlled documentation systems (no electronic document management system), ensuring...  ...presenting documentation Collaborate cross-functionally with QA, Manufacturing, Engineering, and Validation teams to support documentation... 

    Harba Solutions Inc.

    Fishers, IN
    21 hours ago
  •  ...Quality Assurance Document Management This is a 100% onsite position. Assists in maintaining a compliant, efficient Quality Assurance Document Management program. Under direct supervision, perform day-to-day Document Control activities: process DCR packages and review... 

    Collins Consulting

    Worcester, MA
    3 days ago
  •  ...creating a world of pure chemistry! About the role: We are seeking a Document Control Specialist that will report directly to our Quality Manager. This individual will provide support in all aspects of the QA/QC department in processing documentation requests. The role is... 
    Work at office

    iS CLINICAL

    Arizona City, AZ
    4 days ago
  • Legend Biotech is seeking QA Document Control Specialist I/II/III as part of the Quality team based in Raritan, NJ. Role Overview The QA Document Control Specialist role is an exempt level position with responsibilities for supporting the document management process within... 
    Permanent employment
    Contract work
    Temporary work
    Work experience placement
    Local area
    Flexible hours
    Afternoon shift

    Legend Biotech USA

    Raritan, NJ
    1 day ago
  • A leading pharmaceutical company in New Jersey is seeking a QA Document Control Specialist to manage documentation for manufacturing processes. Responsibilities include ensuring compliance with regulations and maintaining accurate records. The ideal candidate holds a Bachelor... 
    Work at office

    Veranova

    Thorofare, NJ
    4 days ago
  • A global biotechnology company is seeking a QA Document Control Specialist I/II/III in Raritan, NJ. This role involves ensuring compliance with GMP documentation processes, supporting both clinical and commercial activities. Candidates need a Bachelor's degree and at least... 
    Full time
    Shift work

    Initial Therapeutics, Inc.

    Raritan, NJ
    4 days ago
  • An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP Document Control operations. This role involves managing an electronic document system, ensuring compliance with policies and procedures, and supporting audits... 

    TechDigital Group

    Summit, NJ
    4 days ago
  •  ...Healthiest 100 Workplaces in America” — is focused on the mind/body/soul of team members through our Culture of Care . Document Control Specialists are responsible for collecting, maintaining and distributing all documents necessary to define product configuration and... 
    Full time
    Work at office
    Monday to Friday
    Flexible hours

    FTI

    Olathe, KS
    21 hours ago