We're looking for a Document Control Specialist II, working in the Pharmaceuticals & Medical Products industry in Sunnyvale, California, United States.
Executes and maintains compliant Quality Assurance Document Management systems and procedures.
Maintains and improves the Document Control Quality Systems in order to support the business and release of drug products and ensures compliance with regulations and established requirements.
Performs administrative tasks to maintain the electronic document management system (EDMS).
Provides user assistance and training on document control and record management systems, processes, and procedures.
We are 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
Bachelor's degree or equivalent professional experience
2 to 5 years of pharmaceutical experience in a GMP environment administering Document Control Systems
2 years of experience using and administering electronic document management tools
Working knowledge of Quality Systems, GMP-related requirements and ICH guidelines
Working knowledge of electronic documentation systems, data retrieval, and electronic file formats
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.