Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job Description
- Receive, evaluate and process test articles for testing
- Communicate and coordinate sample preparation and scheduling with scientific staff and Study Directors
- Determine the surface area and calculate required extraction ratio for test articles submitted for testing
- Prepare samples and dosing solutions according to PSL standard operating procedures and as directed by study protocols using aseptic technique
- Meticulously maintain precise records of all preparations in accordance with Good Laboratory Practices
- Maintain a clean and organized work area
- Ability to safely wear a respirator, as needed
- Follow all PSL safety requirements
- Other duties as assigned
Qualifications
- B.S. or Associate degree in toxicology, biology or equivalent experience in a laboratory environment is preferred.
- Authorization to work in the United States indefinitely without restriction or sponsorship
- Must have working knowledge of medical devices and ISO 10993.
- 1-3 years at a minimum in the CRO or medical device space and GLP experience
- The individual holding this position must be of the highest integrity and have a very strong sense of responsibility. He/she must be mature, well organized, capable of adapting to a broad spectrum of responsibilities and able to maintain meticulous and accurate records.
- Adherence to good laboratory practices (GLP) is of utmost importance. The ability to perform basic mathematical calculations and follow detailed instructions is critical to this role.
Additional Information
Position is full-time, Tuesday - Saturday 8:00am - 5:00pm. Candidates currently living within a commutable distance of South Brunswick Township, NJ are encouraged to apply.
The pay range of this role is from $25/h - $33/h depending on the related experience.
- Excellent full time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
