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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...Suggested
- ...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...SuggestedAll shiftsMonday to Friday
- ...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
$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...SuggestedHourly payMonday to Friday- 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...Suggested
- 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...Suggested
- 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...SuggestedContract work
- 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...Suggested
$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...SuggestedFull timeLocal areaMonday to Friday- 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...SuggestedContract work
- 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...SuggestedContract work
- ...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...SuggestedDay shift
$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...SuggestedHourly pay$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...SuggestedTemporary workWork at officeImmediate startMonday to Friday$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...SuggestedHourly pay$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- 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
- ...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...
- 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
- ...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...
- ...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 payTemporary workWork experience placementFlexible hours
$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- ...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...
- ...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...
- ...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
- 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 employmentContract workTemporary workWork experience placementLocal areaFlexible hoursAfternoon shift
- 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
- 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 timeShift work
- 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...
- ...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 timeWork at officeMonday to FridayFlexible hours

