Biocompatibility Strategy Director (Regulatory Science)

Eurofins Scientific

United States

Remote

USD 150,000 - 210,000

Full time

5 days ago
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Benefits offered by this job

Medical insurance (health)
Dental insurance
Vision insurance
401(k) match
PTO

Job summary

Eurofins Scientific is seeking a senior leader to drive the scientific and commercial strategy for its medical device biocompatibility business. You will mentor staff, support Study Directors in compliant study conduct, and engage with clients and industry bodies to elevate Eurofins as a recognized leader in regulatory science.

The role requires an advanced degree with Ph.D. preferred, 10+ years in biocompatibility or regulatory science, and deep knowledge of ISO 10993, FDA guidance, EU MDR, and

Qualifications

  • Ph.D. preferred; advanced degree in biology, toxicology, biomedical engineering, or related discipline.
  • Minimum 10 years of experience in medical device biocompatibility or regulatory science.
  • Strong knowledge of ISO 10993, FDA guidance, EU MDR, and GLP requirements.

Responsibilities

  • Lead the scientific and commercial strategy for PSL’s medical device biocompatibility business.
  • Mentor technical staff and support Study Directors in regulatory-compliant study conduct.
  • Engage with clients and industry organizations to establish PSL as a recognized leader.

Skills

Regulatory science
Biocompatibility
Leadership
Client engagement

Education

Advanced degree in biology, toxicology, biomedical engineering, or related discipline; Ph.D. preferred

Job description

Eurofins Scientific is seeking a senior leader to drive the scientific and commercial strategy for its medical device biocompatibility business. You will mentor staff, support Study Directors in compliant study conduct, and engage with clients and industry bodies to elevate Eurofins as a recognized leader in regulatory science.

The role requires an advanced degree with Ph.D. preferred, 10+ years in biocompatibility or regulatory science, and deep knowledge of ISO 10993, FDA guidance, EU MDR, and

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