Qa Documentation - 101+ job offers

Actalent

QA Documentation Associate Urgently hiring a QA Documentation Associate in Grove City, OH. An ideal candidate will have at least 6 months of regulatory or quality documentation experience. This is a great opportunity to get your foot in the door and grow within this company! Job Description The Qual

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, review document change req

City of New York

Company Description Job Description DCAS's mission is to make city government work for all New Yorkers. From managing New York City's most iconic courthouses and municipal buildings, to purchasing over $1 billion annually in goods and services for more than 80 City agencies what we do ensures that a

TUV SUD America Inc., a global leader in testing, inspection and certification, has an immediate opening for a Documentation QC/QA Associate position available based in Peabody, MA. Your responsibilities will include, but are not limited to: Assist certification coordinators and specialists in ways

Manpower Group Inc.

Our client, a leading Pharmaceutical & Biotech Manufacturing company, is seeking a QA Associate (GMP Documentation Reviewer) to join their team. As a QA Associate, you will be part of the Quality Assurance department supporting Analytical, QC, and Manufacturing operations. The ideal candidate wi

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, review document change req

QA Documentation Specialist - I Contract Job Description Processes 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 reco

We are seeking a detail-oriented QA Documentation and FAI Technician to maintain the integrity of our quality records and manufacturing specifications. You will be responsible for ensuring all Quality documentation (e.g., Quality Control Instruction, test reports, FAIRs, and Quality SOPs) is accurat

AmbioPharm, Inc.

Summary Seeking a detail‑oriented intern to support the Quality Assurance (QA) Documentation team with organizing, digitizing, and managing GMP records. Great opportunity for students in Business Administration, Life Sciences, or anyone seeking professional office experience. Responsibilities Scan a

A biomedical research company located in Auburn, California, is seeking a Quality Assurance professional to support daily QA activities. The role involves monitoring compliance with GMP and contributing to overall QA system development. Candidates should have a Bachelor's degree in the biological sc

A leading consulting services provider in Winchester, KY, is looking for a Quality Assurance Associate to join their team. The right candidate will have a BS degree in Chemistry or Biochemistry, along with a minimum of 3 years of experience in GMP environments. Responsibilities include reviewing ana

Business Analyst (ERP/UAT) – requiring 3 years experience in BRDs, User Stories, UAT (planning & execution), test case development, QA/QC, process documentation, data analysis, and Oracle PeopleSoft/ERP projects (preferred) with Agile experience.-Onsite-Tallahassee, FL - About the Project OSCA i

Gilead Sciences Inc

Job Description Everyone at Kite is grounded by one common goal - curing cancer. Every day, we seek to establish a direct connection between that purpose and our work. Reporting to the Sr. Manager, Document Control, the QA Documentation Specialist I supports GMP documentation lifecycle activities wi

Nomilk2day

*Deze opdrachtgever heeft voor deze vacature Nomilk2day exclusief geselecteerd als enige recruitment partner.** *HIGHLIGHTS** Join a trusted North American food ingredients distributor as a QA-Regulatory Documentation Manager. In this role, you'll ensure regulatory compliance across all ingredient p

DCAS's mission is to make city government work for all New Yorkers. From managing New York City’s most iconic courthouses and municipal buildings, to purchasing over $1 billion annually in goods and services for more than 80 City agencies what we do ensures that all agencies can deliver on their mis

Stahlbush Island Farms

Job Description Job DescriptionThe 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 requests. Responsibil

Actalent

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, and formatting. Responsibi

SGS Consulting

*Description:** *100% on-site** The QA Engineer is responsible for ensuring the timely development, review and approval of all engineering, validation and lifecycle documentation, (i.e. SOPs, Change Controls, CAPAs, Deviations), ensuring compliance with corporate procedures, SOPs, cGMP, standards an

Katalyst Healthcares & Life Sciences

*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, engineering, validation,

Description We are seeking a detail-oriented QA Documentation and FAI Technician to maintain the integrity of our quality records and manufacturing specifications. You will be responsible for ensuring all Quality documentation (e.g., Quality Control Instruction, test reports, FAIRs, and Quality SOPs