No Software QA/Automation please!!
No H1B and/or C2C please!!
One of our leading Pharmaceutical client is looking for a Quality Assurance Specialist (Biologics Document), who will be responsible for tracking and monitoring Process Validation progress and deliverables. Also Coordinate Process Validation documentation.
Job Title: Quality Assurance Specialist (Biologics Document)
W2 Contract & Onsite role
Work Location: Foster City, CA
Required Experience:
- Minimum of four years experience in biotechnology, process validation, Quality, or a related area
- Must have understanding and application of GMP principles, concepts, and practices
- Knowledge of biochemical manufacturing process and terminology
- Strong project management skills
Responsibilities:
- Create, revise, and implement procedures, best practices, and business processes for the Biologics Process Validation program
- Act as a Project Manager to track and monitor Process Validation progress and deliverables
- Coordinate Process Validation documentation: Prepare, edit, proofread, coordinate and adjudicate reviewer comments with author and subject matter experts
- Perform Data Verification of completed Process Validation studies and reports
- Create study templates to drive alignment
- Work across Quality Assurance, Process Development, MSAT, and Contract Manufacturing Organizations
If you are a right fit and this job excites you then please apply quick!!
