Job Description
Work Flexibility: HybridPlan, execute, evaluate, and document biocompatibility studies and justifications in support of product safety and performance tests. And support product transfers to other plants/facilities. Partners with cross-functional project team members to define evaluation / verification strategies of medical devices and review, evaluate, interpret, and apply internal and external guidance documents as they relate to biocompatibility. Identify and analyze materials, design, and process challenges to achieve optimal solutions that satisfy cost and technical requirements as they relate to biological safety. Responsible for identifying critical process factors and their effects on biological safety. Develop technically sound test campaigns (i.e. biocompatibility and chemical testing)., protocols, reports, regulatory summaries, and verification of methods and results in collaboration with project team, test...
What you will do: