We're looking for a Quality Control Analyst III, working in the Biotechnology/Medical Devices industry in Novato, California, United States.
Develops framework for critical materials management including inventory and documentation management.
Supports and develops statistical trending processes for stability, lot release and reference standard results.
Creates and/or revises SOPs.
Initiates and investigates deviations and CAPAs in validated system (e.g. Trackwise).
Supports GMP activities including regulatory agency audits and LIMS data management.
We're offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
B.S and/or M.S. in Biology or Biochemistry or similar field with 3-5 years of GMP experience.
Excellent knowledge of GMPs.
Experience with regulatory agency audits.
Experience with LIMS for data management and Trackwise for deviation/CAPA management.
Experience in statistical trending of stability, lot release and reference standard data.
Team player and work in collaboration with various groups within and outside quality control.
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.