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- DEKA Research & Development in Manchester, NH, is looking for a QA Admin focusing on Document Control. This role supports the Quality Management System by managing document control processes in a medical device research environment. Responsibilities include performing document...SuggestedWork at office
$27.56 per hour
A national staffing firm is seeking a QA Associate for a prominent client in Mountain View, CA. The role involves providing clerical and administrative support for documentation processes, including scanning, verifying, and archiving documents. Candidates should possess...Suggested- ...reputable staffing company in Maryland is seeking a detail-oriented candidate to provide clerical and administrative support related to documentation processes. Responsibilities include maintaining controlled documents and records, ensuring data input accuracy, and assisting...Suggested
- A staffing and consulting company is looking for a QA Document Control Associate to provide clerical and administrative support in documentation processes. The role involves creating logbooks, maintaining document archives, filing controlled documents, and ensuring data...Suggested
- ...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
- 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
- ...leading company in food and beverage based in California seeks a Documentation Specialist for Quality Assurance and Regulatory Affairs. This is a 3-month hybrid contract position, requiring 2+ years of QA experience. Responsibilities include managing quality documentation...SuggestedContract work
$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$31 - $35 per hour
...recruitment firm in Los Angeles is seeking a detail-oriented Documentation Specialist to cover a maternity leave for a leading health supplement... ...hybrid role requires strong Excel skills and at least 2 years of QA/Regulatory experience in the food or dietary supplement...SuggestedHourly payContract workImmediate start- 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
- 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
$20 - $22 per hour
A staffing and consulting firm in Elgin, IL is seeking a meticulous Quality Assurance Document Specialist responsible for ensuring the accuracy and completeness of quality documentation. This role involves regular review of batch records and adherence to SOPs, with scheduled...SuggestedHourly payAfternoon shift- 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
- ...construction materials and workmanship, ensuring compliance with established standards. Duties include maintaining construction documentation and assisting in monitoring regulatory compliance. The ideal candidate has a high school diploma, NICET level 3 certification, and...Suggested
- The Associated General Contractors Of America is hiring a Construction Manager Technician in Middletown Township, Pennsylvania. This role involves inspecting construction materials and workmanship on projects to ensure compliance with standards. Key requirements include...SuggestedFor contractors
- A leading pharmaceutical company in West Warwick is seeking a Documentation Coordinator to maintain and control GMP documentation according to FDA regulations. The role requires managing the document lifecycle, supporting inspections, and ensuring compliance with quality...
- **Number of Openings: 1****Home-Based QA, Documentation & Executive Support Specialist** to join our DCX team. In this role, you will work closely with the CEO of a growing technology and consulting firm, supporting software quality assurance, documentation, client onboarding...Permanent employmentFull timeWork from homeMonday to FridayShift workNight shift
- 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
- ...Job Title: QA Document Control Specialist Location: Central Islip, NY 11722 Work Hours/Shift: Onsite, 8:30 AM - 5:00 PM (Monday - Friday) Position Overview The QA Document Control Specialist will play a key role in managing, organizing,...Monday to FridayShift work
- ...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
$62.5k - $93.7k
MilliporeSigma is seeking a Quality Assurance Document Control Specialist in St. Louis, Missouri. This position involves supporting documentation systems, ensuring compliance with regulations, and managing document creation and distribution. Ideal candidates should have...$70.67k - $92.76k
QA Document Control Specialist I/II/III Legend Biotech is a global biotechnology company dedicated to treating life‑threatening diseases. Headquartered in Somerset, New Jersey, we develop advanced cell therapies across multiple technology platforms. Role Overview The...Work experience placementFlexible hours- An established industry player is seeking a detail-oriented QA Associate Specialist to enhance their Document Control operations. This role is vital in supporting the cGMP Document Control processes, including document approvals and change control. The ideal candidate will...
- A leading biotechnology firm in Raritan, New Jersey, is seeking a QA Document Control Specialist to support the document management process within its manufacturing facility. The ideal candidate will have a Bachelor's degree in a related field and at least 2 years of experience...
- A design firm is seeking an Architectural Document Quality Control Associate in Collegeville, PA. The role involves reviewing construction documents for accuracy, collaborating with teams to resolve project issues, and interacting with clients to implement changes. Candidates...
- Job Title: Quality Assurance Document Control (QADC) Associate Specialist Location: Bothell, WA*Onsite Shift: Friday- Monday 2pm-10:30pm Top Skills: Strong communication and customer service skills. Innovation Able to prioritize, manage time well, multi-task, and troubleshoot...Local areaShift work
$54.5k - $65k
...for their Quality Assurance department. This role involves managing electronic quality systems, providing training and oversight on document control, and ensuring compliance with GMP practices. Candidates should have an Associate’s degree and 2+ years of experience in a...- 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 regulatory standards, and supporting audits...
- An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP Document Control operations. This role involves managing document change control processes, issuing batch records, and ensuring compliance with regulatory...
