Biocompatibility Specialist
StrykerAbout the role
Stryker is hiring a Biocompatibility Specialist in Weston, Florida to support Joint Replacement! In this non-laboratory-based role, role, you will be performing biocompatibility assessments to determine product safety of the entire product portfolio.
What You Will Do:
Support decisions regarding chemistry and biocompatibility testing; role is conducted in a non-laboratory setting.
Support new product development and/or changes to medical devices currently on the market for biocompatibility/toxicology.
Support biocompatibility toxicological assessments, produce test data, and present results to cross-functional team.
Contribute to departmental initiatives.
Write technical and scientific documentation.
Support cross functional teams including (RA, AO, Ops) to ensure business unit project timelines are met.
Engage with team by supporting the development, maintenance, and improvements of the policies and procedures related to biocompatibility.
Participate in root cause analysis, problem solving, and out-of-specification investigations.
Contribute to validation & verification activities (i.e. product adoptions, testing plans, etc.).
What you need:
Required:
BS in Chemistry/Biochemistry/Toxicology or related discipline
0+ years related experience, medical device or pharmaceutical.
Preferred:
Strong self-motivation and able to take initiative!
Eager to learn and take on different challenges!
1+ years related experience, medical device, pharmaceutical or chemical industry
Knowledge of GDP, ANSI, AAMI, ISO, FDA, and USP guidelines related to biocompatibility assessments (i.e. ISO 10993, ISO 22442, etc.).
An effective communicator and can prioritize and manage multiple tasks simultaneously.
Strong problem-solving skills with a proactive, solution-focused mindset.
- Demonstrated ability to write technical documentation.
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