Biocom Materials Engineer
o Evaluating medical device products for safety per internal procedures, US and international regulations, and the ISO 10993 Standard series.
o Assisting in the design and implementation of biocompatibility testing systems and procedures for Ethicon and across the Johnson & Johnson Medical Device sector.
o Ensuring appropriate documentation is established and maintained to support that the biocompatibility and toxicity testing meets all US and international test requirements per ISO, FDA (US Food and Drug Administration), and GLPs (good laboratory practices).
o Coordinating, designing, implementing, and analyzing testing systems, procedures and test results for biocompatibility / toxicology evaluations and in vivo / in vitro studies.
o Reviewing, interpreting, and summarizing toxicological and material chemistry raw data from reports.
o Applying technical expertise to solve complex biocompatibility problems, utilizing ingenuity and business experience.
o Serving as the sponsor for applicable GLP / non-GLP biocompatibility studies per current, global regulatory and compliance requirements.
o Very strong in medical grade Materials identification and release process.
o Strong in Medical device standards.
Top Skills:
Biocompatibility testing Knowledge
Validating Toxicologist reports
Medical grade materials
Additional Details:
B.E. Mechanical , Biotechnology or Equivalent
Faizan Shaikh
Employers have access to artificial intelligence language tools (AI) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job
Dice Id:
10217521
Position Id:
8724721
o Evaluating medical device products for safety per internal procedures, US and international regulations, and the ISO 10993 Standard series.
o Assisting in the design and implementation of biocompatibility testing systems and procedures for Ethicon and across the Johnson & Johnson Medical Device sector.
o Ensuring appropriate documentation is established and maintained to support that the biocompatibility and toxicity testing meets all US and international test requirements per ISO, FDA (US Food and Drug Administration), and GLPs (good laboratory practices).
o Coordinating, designing, implementing, and analyzing testing systems, procedures and test results for biocompatibility / toxicology evaluations and in vivo / in vitro studies.
o Reviewing, interpreting, and summarizing toxicological and material chemistry raw data from reports.
o Applying technical expertise to solve complex biocompatibility problems, utilizing ingenuity and business experience.
o Serving as the sponsor for applicable GLP / non-GLP biocompatibility studies per current, global regulatory and compliance requirements.
o Very strong in medical grade Materials identification and release process.
o Strong in Medical device standards.
Top Skills:
Biocompatibility testing Knowledge
Validating Toxicologist reports
Medical grade materials
Additional Details:
B.E. Mechanical , Biotechnology or Equivalent
Faizan Shaikh
Employers have access to artificial intelligence language tools (AI) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job
Dice Id:
10217521
Position Id:
8724721
Job ID: 488998620
Originally Posted on: 8/11/2025
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