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- ...Qa Documentation Specialist Visa status: U.S. citizens and those authorized to work in the U.S. are encouraged to apply. Tax terms: W2, 1099 Corp-Corp or 3rd parties: yes Foster City, CA local candidates only Required to come in the office at a minimum of 3 days...SuggestedWork at officeLocal areaFlexible hours3 days per week
Keylent Inc
San Mateo, CA1 day 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, NJ3 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...Suggested
- A leading QA services provider is seeking a QA Documentation Specialist III in Tampa, FL, for a 12-month on-site role. The specialist will be responsible for the timely development and approval of engineering and validation documentation. Key responsibilities include ensuring...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
- 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
$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- Role Summary The Quality Assurance Documentation Specialist I is a quality-focused individual who ensures documentation and record keeping processes conform to approved procedures and output documents are accurate. This role will support the organization by maintaining...SuggestedFor contractors
$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- ...effective corrective and preventative actions (CAPAs) Translate complex technical scenarios into clear, concise, and audit-ready documentation Identify trends across deviations, nonconformances, and quality events to support continuous improvement initiatives Manage...Suggested
$40 - $41 per hour
JOB TITLE: QA Documentation Specialist III LOCATION: Tampa, FL DURATION: 12 Months Pay rate: $40-$41 per hour 100% on-site Summary: The QA Engineer is responsible for ensuring the timely development, review and approval of all engineering, validation and lifecycle documentation...SuggestedHourly payLocal area$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- ...seeking dental hygienists or assistants to transition into administrative roles. This position involves ensuring quality control in documentation and contributing to the preparation and review of healthcare R&D studies. Ideal candidates will have a background in dentistry...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
- 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...Contract work
- ...leading company in the food and beverage industry is seeking a Documentation Specialist to support its Quality Assurance team during maternity leave... .... Ideal candidates should have 2+ years of experience in QA/Regulatory roles within food or beverage industries and a bachelor...Contract work
- A leading pharmaceutical company in New Bedford seeks a Quality Assurance Documentation Specialist I to maintain essential documentation for compliance with quality management standards. This role includes managing document workflows, issuing batch records, and ensuring...Full time
$33 - $35 per hour
A well-known health supplement company is seeking a Documentation Specialist to cover maternity leave for 3 months. The role involves maintaining quality and regulatory documentation to ensure compliance while supporting the Quality & Regulatory team. Ideal candidates...Hourly payWork 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
- ...services company in Minnetonka is seeking a Commercial Quality Assurance Associate III. This role involves reviewing commercial loan documentation to ensure accuracy and compliance with regulatory standards. The ideal candidate holds a Bachelor’s degree and has 5-7 years of...
- ...wealth bank in Minnesota is seeking a Commercial Quality Assurance Associate III. This position involves reviewing commercial loan documentation for accuracy and compliance, conducting portfolio management, and training team members. The ideal candidate will have a...
- ...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
Manpower Group Inc.
Bridgeton, NJ4 days ago - ...Document Control Specialist You've discovered something special. A company that cares. Cares about leading the way in construction, engineering, manufacturing and renewable energy. Cares about redefining how energy is designed, applied and consumed. Cares about thoughtfully...Full timeWork at officeMonday to FridayFlexible hours
- ...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...
$30 - $35 per hour
...Job Description Job Description Job Title: Quality Assurance Documentation Specialist Job Description We are seeking a dedicated Quality Assurance Documentation Specialist who will play a crucial role in supporting the building and control of Standard Operating...Contract workTemporary workMonday to FridayActalent
Fairfield, Essex County, NJ15 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...
- 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
- 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...
