Eurofins: Study Director - Biocompatibility Studies — South Brunswick Township, NJ, United States

About Eurofins

Eurofins provides analytical testing and laboratory services across life sciences and other industries. Its work includes assessing food, water, pharmaceutical and cosmetic products for qualities such as safety, authenticity, composition and accurate labelling. The employer also describes activities in genomics, clinical-study support, biopharmaceutical development and manufacturing, and diagnostic testing. Scientific methods and dependable information are central to this business, supported by the technology and operational functions used to deliver laboratory services.

The position and its setting

Eurofins lists Study Director - Biocompatibility Studies in South Brunswick Township, NJ, United States, under reference REF80230V. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

• Department: Testing & Laboratory
• Employment type: Full-time
• Employer listing date: 23 October 2026
• Legal Entity: CUS027 - Eurofins Lancaster Laboratories, LLC
• Contract Type: Permanent
• Business Lines: Other Business Line
• Brands: Eurofins USA BioPharma Services

Responsibilities and work described

• Supervise and assist in the conduct of regulatory studies performed
• Responsibilities include:
• Supervise study conduct
• Support: protocol development, design and implementation
• Responsibilities as stated in GLP regulations
• Data interpretation and report writing
• Client liaison
• Management Responsibilities:
• Overall, day-to-day laboratory operation including supervision of technical staff assigned to your studies
• Scheduling and coordinating initiation and conduct of studies
• Quality / delivery: that the study schedule and financial aspects of each study that you are responsible for are accurately tracked on a regular basis
• Technical Responsibilities:
• Overall responsibility for the technical conduct of all studies and interpretation, analysis, documentation and reporting of results
• Specifically:
• Establishment: test protocols and corresponding SOP's
• Development: experimental design and supervise implementation of experiments (tests)

Essential requirements and candidate background

• Safely wear a respirator required
• 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
• Intimate working familiarity and/or ability to quickly learn and develop such familiarity with all government regulations dealing with testing particularly EPA, FDA, DOT, OECD, and GLP regulations in addition to ISO standards
• Hands-on working knowledge of the tests that will be under their responsibility
• Good administrative skills and leadership ability
• Must communicate effectively and write well

Location, schedule and contract conditions

For this overseas or regional listing, confirm work authorisation and any location restrictions with the employer. The location does not establish visa sponsorship or permission to work remotely from India.

• Work arrangement: On-site
• Advertised location: South Brunswick Township, NJ, United States

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Study Director - Biocompatibility Studies vacancy is not an offer for reference REF80230V; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Eurofins

Applications follow the official employer page linked below.

Open the official Eurofins posting below and match the title and reference REF80230V.

Compare your qualifications and experience with the essential conditions for the South Brunswick Township, NJ, United States position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: GLP

GLP-related experience should identify the laboratory activity and the controls or records you handled. Explain how work was documented, checked and traceable within the environment you actually worked in.

Relevant skills

• ISO
• GLP
• laboratory testing
• compliance
• microbiology
• chemistry