GLP Regulatory Study Director - Lab Lead

RXinsider LTD.; South Brunswick, Northern (NJ, KY); Hybrid; USD 95,000 - 135,000; Full time

Job summary

Eurofins USA BioPharma Services in Dayton, NJ seeks an experienced supervisor to oversee regulatory studies, ensure GLP compliance, and interpret data. You will develop protocols, train staff, and liaise with sponsors.

This role requires a BS degree, at least five years of biocompatibility study oversight, and strong knowledge of EPA, FDA, DOT, OECD, GLP, and ISO standards. Full-time with weekday hours and potential overtime.

Qualifications

• BS degree in a field related to their area of responsibility.
• Minimum of 5 years experience overseeing biocompatibility studies.
• Familiarity with EPA, FDA, DOT, OECD, GLP regulations and ISO standards.
• Hands-on working knowledge of the tests under their responsibility.
• Strong administrative and leadership skills; effective communication and writing.

Responsibilities

• Supervise study conduct.
• Oversee day-to-day laboratory operations and staff.
• Coordinate initiation and conduct of studies and track schedules and finances.
• Ensure GLP compliance and accurate data reporting.

Skills

Good administrative skills

Education

BS degree

Job description

Eurofins USA BioPharma Services in Dayton, NJ seeks an experienced supervisor to oversee regulatory studies, ensure GLP compliance, and interpret data. You will develop protocols, train staff, and liaise with sponsors.

This role requires a BS degree, at least five years of biocompatibility study oversight, and strong knowledge of EPA, FDA, DOT, OECD, GLP, and ISO standards. Full-time with weekday hours and potential overtime.