Senior GLP Study Director

Eurofins BioPharma Product Testing North America; South Brunswick (NJ); On-site; USD 90,000 - 130,000; Full time

Job summary

Eurofins USA BioPharma Services in Dayton, NJ seeks a seasoned supervisor to oversee regulatory biocompatibility studies, develop and implement test protocols, and ensure GLP compliance across all study phases.

You will supervise technical staff, interpret data, write study reports, and liaise with sponsors and regulatory agencies while coordinating study schedules, budgets and resource needs.

Qualifications

• BS degree in a related field and strong knowledge of GLP regulations.
• Minimum of 5 years experience overseeing biocompatibility studies.
• Familiarity with EPA, FDA, DOT, OECD and ISO GLP standards.
• Ability to lead a team and communicate effectively.
• Capable of training staff and maintaining sponsor relationships.

Responsibilities

• Supervise study conduct.
• Assist in protocol development, design and implementation.
• Ensure GLP compliance across all study phases.
• Data interpretation and reporting.
• Liaise with sponsors and regulatory agencies.
• Manage scheduling and study budgets.
• Instruct and train scientists in procedures.

Skills

Leadership

GLP regulations

Regulatory knowledge

Data interpretation

Scientific communication

Education

BS degree in a related field

Job description

Eurofins USA BioPharma Services in Dayton, NJ seeks a seasoned supervisor to oversee regulatory biocompatibility studies, develop and implement test protocols, and ensure GLP compliance across all study phases.

You will supervise technical staff, interpret data, write study reports, and liaise with sponsors and regulatory agencies while coordinating study schedules, budgets and resource needs.