qa documentation specialist

QA Document Coordinator Job Type: Contract Education: Associate’s Degree Required Job Summary We are seeking a detail-oriented QA Document Coordinator to support document control and administrative activities within a regulated GMP environment. This role will be responsible for maintaining accurate document tracking, scanning and verifying records,...

QA Document Coordinator Job Type: Contract Education: Associate’s Degree Required Job Summary We are seeking a detail-oriented QA Document Coordinator to support document control and administrative activities within a regulated GMP environment. This role will be responsible for maintaining accurate document tracking, scanning and verifying records,...

job summary: Advance your career with a top-tier global pharmaceutical leader in Melrose Park, IL! We are seeking a reliable, detail-oriented QA Documentation Specialist for an immediate, full-time on-site role (Monday-Friday, 8:00 AM-5:00 PM). This 3-month contract position offers strong potential for extension or conversion based on performance and...

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.Join Kite, as we make even...

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.Join Kite, as we make even...

QA Document CoordinatorJob Type: ContractEducation: Associate’s Degree RequiredJob SummaryWe are seeking a detail-oriented QA Document Coordinator to support document control and administrative activities within a regulated GMP environment. This role will be responsible for maintaining accurate document tracking, scanning and verifying records, managing...

Penumbra, Inc. in Alameda, CA is seeking a QA Document Specialist II to support quality processes and regulatory compliance. You will process Engineering Change Orders, verify English usage and Penumbra formatting, and communicate with all levels to maintain document integrity. The role requires a high school diploma or AA with 2+ years in regulated...

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even...

As a QA Document Specialist II, you will play a pivotal role at Penumbra providing timely and accurate support of quality processes related to Document Services to ensure compliance with Penumbra procedures and regulatory requirements. Following standards and procedures and analyzing data, you will develop knowledge of Penumbra processes and external...

Job Responsibilities: Support the implementation, execution and maintenance of the PQS integration and Quality Documents in Veeva at the Vacaville site. Support PQS integration by working with the Quality Document control group to complete workflows, document gating and coordinate elements of the document change process to ensure minimal disruption to...

Job Description We’re hiring a QA Documentation Specialist for our Northwest Houston client! We are looking for experienced, reliable, hard-working employees who can interview immediately! DESCRIPTION OF YOUR DREAM JOB: Job Title: QA Documentation SpecialistLocation: 77008Pay: $20.00/hourHours: Monday–Friday, 8:00 AM–5:00 PMDuration:...

Job Responsibilities: Control record management including receipt, reconciliation, scanning and verification, record check-out/check-in and maintain scanned record back-ups Controlled document issuance and tracking Support audit activities Controlled numbering, issuance and tracking Perform other duties as assigned Skills: 3-5 Years Experience ...

QA Documentation Specialist Location: San Diego, CAType: Full TimeIndustry: Pharmaceutical ManufacturingPosition OverviewOur client is seeking a QA Documentation Specialist to support the development, revision, and review of GMP manufacturing documentation. The ideal candidate will have pharmaceutical or life-sciences experience and a strong...

Job Responsibilities: Support the implementation, execution and maintenance of the PQS integration and Quality Documents in Veeva at the Vacaville site. Support PQS integration by working with the Quality Document control group to complete workflows, document gating and coordinate elements of the document change process to ensure minimal disruption to...

Job Responsibilities: Support the implementation, execution and maintenance of the PQS integration and Quality Documents in Veeva at the Vacaville site. Support PQS integration by working with the Quality Document control group to complete workflows, document gating and coordinate elements of the document change process to ensure minimal disruption to...

Job Title: QA Documentation Specialist I Job Duration: 6 months (onsite) Job Location: Vacaville, CA. 1st shift: M-F (8am - 5pm) Job Description: We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process...

Company DescriptionIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide...

Summary: The QA Specialist primary responsibility is the review and approval GMP documentation associated with Site operations, to include Manufacturing, Validation, MES, and Quality Control. This role is to serve as a Subject Matter Expert (SME) for QA document review relevant to Equipment/Instrumentation, Validation Maintenance, and relevant...

Job DescriptionProcesses IT controlled documents such as computer system procedures, forms, specifications and test documentation in the Electronic Document Management System (EDMS) following defined processes/procedures. Scans, verifies and archives IT records in accordance with record retention requirements. Ensures the consistent application of Good...

M-F 5x onsite 1st shift (8am - 5pm) We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process with document control and PQS integration, ensuring compliance with cGMP and global requirements. Key...