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- A nuclear technology company in Bellevue, WA is looking for a Document Control Specialist. This full-time position requires an associate degree and 3+ years of experience in document control in the nuclear energy sector. The responsibilities include managing regulatory...SuggestedFull time
- A biotechnology company in Raritan, NJ is looking for a Document Control Specialist to manage and support the document management process in a GMP environment. The role involves reconciling GMP documents, creating logbooks, and ensuring the compliance of document storage...Suggested
- A leading global manufacturer in St. Louis, MO, is seeking a QC Documentation Specialist for the Day Shift (M-F). This role involves processing Raw Material documentation, responding to customer inquiries, and supporting quality improvement initiatives. Ideal candidates...SuggestedDay shift
- A biotechnology company is seeking a QA Document Control Specialist I/II/III in Raritan, NJ to support document management in a GMP environment. The ideal candidate will have a Bachelor's degree in a relevant field and at least 2 years of related experience, preferably...SuggestedAfternoon shift
$22.6 - $38 per hour
Document Associate, QA Job Title: Documentation Specialist Location : Bedford, Ohio Job Type : Full-time About Us: As a developer, manufacturer... ...management system SKILLS Ability to write, revise and review SOPs Strong interpersonal skills and great attention to detail...SuggestedHourly payFull timeWork at office$21 - $23 per hour
...mission-driven team. Position Overview We are seeking a Legal Document Specialist with a legal or paralegal background to support our... ...Key Responsibilities Prepare and Edit Legal Affidavits : Draft, review, and edit service of process affidavits for accuracy, completeness...SuggestedHourly payFull timeFlexible hours- Document Controller - Environment Division Location - Hampton, Middlesex Purpose of the Role Provide a consistent support to project teams... ..., RDD, RFI and Change Control within our system(s) Carry out QA check within agreed Workflows. Support the Commercial and Design...SuggestedFull timeContract workFor contractorsApprenticeshipFor subcontractorWork at office
$22 per hour
We’re seeking a Document Control Assistant to work at a leading organization in Dallas, TX.... ...Writing, updating, issuing, and maintaining QA documents such as SOPs, Work Instructions... ...control process. Coordinating periodic review of SOPs and collaborating with subject...SuggestedTemporary workWork experience placementWork at officeLocal areaMonday to FridayShift work- A healthcare organization in St. Louis seeks a Document Coordinator II responsible for managing quality assurance documents. Key duties include document control, label reconciliation, and training employees on document management systems. Candidates should have a high...SuggestedWork at office
- ...company in Wichita, Kansas is seeking a Quality Assurance Assistant to ensure compliance in a GMP environment. The role involves reviewing documentation, supporting manufacturing processes, and conducting assessments. Candidates should be detail-oriented with a relevant high...Suggested
- ...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....SuggestedWeekly payTemporary workWork experience placementFlexible hours
Manpower Group Inc.
Bridgeton, NJ1 day ago - ...Description: Implement, control and coordinate changes in documentation. Facilitates the updating and routing of controlled documents,... ..., Master Forms and Master Batch Records within the eDMS. Review documents, review document change requests and route document...Suggested
Katalyst Healthcares and Life Sciences
Neshanic Station, NJ1 day ago $68.8k - $123.8k
The QA Document Control Quality Specialist III maintains, develops, and supports the Jabil Gurnee Quality Document System, driving efficiency... ...way to employees. Support Bi-Annual Quality Management Review by working with the Quality Engineers, Quality Control and Quality...SuggestedWork at office- A leading manufacturing company is seeking a QA Document Control Quality Specialist III to manage the quality document system and ensure compliance with regulatory requirements. Responsibilities include modifying documents, collaborating with cross-functional teams, supporting...Suggested
$31 - $44 per hour
Documentation Specialist - covering a maternity leave. El Segundo, CA (Hybrid - Tues/Thurs in... ...Specialist. Expect a healthy mix of: Reviewing and maintaining quality & regulatory documentation... ...ERP systems and SharePoint 2+ years of QA/Regulatory experience Bachelor’s degree...SuggestedPermanent employmentContract workWork at officeLocal areaImmediate startRelocationMonday to Friday- POSITION DESCRIPTION Title: Training and Documentation Specialist Classification: Salaried, exempt Position Type: Full Time Reports to: Director... ...and version control, and overseeing Quality Assurance (QA) processes for continuous compliance and strategic improvement....Full timeWork experience placement
- ...Document Control Specialist You've discovered something special. A company that cares. Cares about leading the way in construction,... ...the lives of team members and their families. You're invited to review the full list of FTI benefits available to regular/full-time team...Full timeWork at officeMonday to FridayFlexible hours
$38.41 - $41.55 per hour
...To provide a comprehensive Quality compliance review of cGMP analytical data and results for raw... ...systems, operations and personnel relating to the QA Data Review process. Writes and revises SOP's and other GMP documentation as needed. Ensures all work is performed...Hourly payAmerican Regent, Inc.
Shirley, NY2 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... ...PM - 12:30 AM Key Responsibilities Serve as a Document Control reviewer for new and revised procedures and documents to ensure...Permanent employmentContract workTemporary workWork experience placementLocal areaFlexible hoursAfternoon shift
- 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...
- ...Quality Assurance Document Management This is a 100% onsite position. Assists in maintaining a compliant, efficient Quality Assurance... ...-to-day Document Control activities: process DCR packages and review for correctness and completeness; monitor and... Collins Consulting
- 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...
$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...Hourly pay- A leading biotechnology company is seeking a Manufacturing Documentation Specialist II in Hercules, California. This role requires collaboration with the Quality department to manage change requests, review and create various documents, and maintain the Document Storage...
- Role Summary The Quality Assurance Documentation Specialist I is a quality-focused individual who ensures documentation and record keeping... ...packaging batch records to meet production schedule requirements. Review records for accuracy and good documentation practices. Provide...For contractors
- 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...
- ...complex technical scenarios into clear, concise, and audit-ready documentation Identify trends across deviations, nonconformances, and... ...instructions, specifications, and batch records Issue, reconcile, and review GxP documentation to ensure compliance with internal standards...
$70.67k - $92.76k
QA Document Control Specialist I/II/III Legend Biotech is a global biotechnology company dedicated to treating life‑threatening diseases... ...reconciliation. Key Responsibilities Serve as a Document Control reviewer for new and revised procedures and documents to ensure...Work experience placementFlexible hours- 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...
