We're looking for a Associate Compliance Manager, working in the Biotechnology/Medical Devices industry in Foster City, California, United States.
Define and develop a global supplier management process.
Define and develop a vendor selection process.
Assist with supplier qualification activities of new and existing suppliers in support of clinical and commercial manufacturing activities.
Manage supplier changes and risk evaluation activities including supplier onboarding, supplier inactivation, change in material/services provided, name and location.
Proactively communicate supplier changes within SMA that impact activities such as QP release, audit scheduling, Quality Agreements, etc.
The pay range we're offering is 90 to 97 per hour. This position may present an opportunity to go permanent.
Our client is a people driven staffing company. Growing fast - 33% annually!
How? Building trusting relationships with top candidates. Like you! You’ll get one-on-one time focused on your skills, needs, and discovering opportunities in which you’ll thrive. The goal is to place you in the right position for you and your goals.
Where? Top IT and telecommunications companies. You’ll make a difference and grow in Technology, Government Services, Professional Services, or Engineering.
Helping you achieve your goals! It’s the right way and the only way to succeed in staffing.
Experience Required for Your Success
10+ years of relevant experience in the pharmaceutical industry and a BS or BA or 8+ years of relevant experience and an MS
Strong working knowledge of cGMP (FDA, EU, and ICH) requirements and the ability to assess compliance risks
Experience with supplier management and auditing
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.