Study Director, GLP Biocompatibility & Protocols

Eurofins USA BioPharma Services; Brunswick (GA); On-site; USD 90,000 - 130,000; Full time

Job summary

Eurofins USA BioPharma Services is seeking a qualified professional to supervise regulatory studies, oversee GLP-compliant protocols, and lead technical teams. You will develop and supervise study design, interpret data, and maintain sponsor communications.

The role emphasizes quality, regulatory compliance, and leadership in a fast-paced laboratory environment, with a focus on safety, protocol adherence, and timely reporting.

Qualifications

• BS degree in a field related to their area of responsibility (e.g. animal science, chemistry, biology, microbiology).
• Minimum of 5 years' experience overseeing biocompatibility studies.
• Extensive knowledge of EPA, FDA, DOT, OECD, GLP and ISO regulations.
• Hands-on knowledge of the tests under their responsibility.
• Strong communication, leadership and writing skills.

Responsibilities

• Supervise study conduct and data interpretation.
• Assist in protocol development, design, and implementation.
• Ensure GLP compliance and regulatory reporting.
• Maintain sponsor liaison and communicate test results.
• Oversee day-to-day lab operations and scheduling.

Skills

Administrative skills

Leadership

Communication

Technical writing

Education

BS degree in life sciences or related

5+ years experience overseeing biocompatibility studies

Job description

Eurofins USA BioPharma Services is seeking a qualified professional to supervise regulatory studies, oversee GLP-compliant protocols, and lead technical teams. You will develop and supervise study design, interpret data, and maintain sponsor communications.

The role emphasizes quality, regulatory compliance, and leadership in a fast-paced laboratory environment, with a focus on safety, protocol adherence, and timely reporting.