Senior GLP Study Director & Lab Lead

Eurofins USA BioPharma Services; Ten Mile Run (NJ); On-site; USD 70,000 - 100,000; Full time

Job summary

Eurofins USA BioPharma Services seeks a qualified supervisor to oversee regulatory studies, ensure GLP compliance, and interpret data. You will assist in protocol development, design, and reporting while supervising scientific staff. Position is full-time, Monday–Friday, with overtime as needed.

Minimum 5 years of experience in biocompatibility studies and a BS degree in a related field are required; strong regulatory knowledge of EPA, FDA, DOT, OECD, and ISO standards is essential.

Qualifications

• BS degree in a related field (e.g. animal science, chemistry, biology, microbiology).
• Strong leadership and oversight experience in regulated studies.
• Solid understanding of GLP, EPA, FDA, DOT, OECD and ISO standards.

Responsibilities

• Assist in protocol development, design and implementation.
• Ensure GLP compliance and proper data interpretation and reporting.
• Supervise and train technical staff across regulatory studies.

Skills

Leadership

Regulatory knowledge

Data interpretation

Written communication

Education

BS degree in a related field

Tools

GLP SOPs

Job description

Eurofins USA BioPharma Services seeks a qualified supervisor to oversee regulatory studies, ensure GLP compliance, and interpret data. You will assist in protocol development, design, and reporting while supervising scientific staff. Position is full-time, Monday–Friday, with overtime as needed.

Minimum 5 years of experience in biocompatibility studies and a BS degree in a related field are required; strong regulatory knowledge of EPA, FDA, DOT, OECD, and ISO standards is essential.