QA Documentation Specialist I - Pharmaceutical Manufacturing

SRG, the leader in the Life Sciences human capital industry, is looking for a full-time, contract Quality Assurance Document Specialist I to join our client's pharmaceutical manufacturing team in Vacaville, Ca. This position provides support to the Quality System Management process with document control and PQS integration, ensuring compliance with cGMP and global requirements.

*W2 contracts only, no C2C.

Must Haves:

• 1-3 years of experience in Quality within the pharmaceutical or biopharmaceutical industry
• Understanding of supplier quality function
• Preferred experience with Veeva Quality Document Management System and Microsoft Teams, CAPA, Document oversight
• Preferred Technical writing experience

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 site operations
• Initiating and management of documents in Veeva Quality Docs.
• Formating and editing of control documents
• Track and log request of source documents
• Ensure all activities are conducted in compliance with cGMP and global requirements.

**Only candidates selected to be moved forward in the recruitment process will be contacted by SRG's Recruitment Team to schedule a conversation.

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting [email protected] or fill out this form to request accommodations.