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 Organisation 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 Organisations. It also has a rapidly developing presence in highly specialised 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 decentralised 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.
*THIS IS NOT A DATA SCIENCE POSITION*
Employee Responsibilities:
Gain a technical understanding of the techniques for the assays in which review is being performed
Begin to gain industry knowledge of the testing being completed within the department
Document work as required for GMP compliance
The Ideal Candidate would possess:
One to two years experience in molecular and/or cell biology, mainly real-time PCR, ddPCR, ELISA, cell based plate reader, and nucleic acids sequencing.
Strong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Minimum Qualifications:
Bachelor’s degree in molecular/cellular biology or other related degree concentration, or equivalent directly-related experience.
At least one to two years hands on experience in a molecular/cell biology laboratory; industry and/or contract testing experience desired
Familiarity or experience with GMP setting highly preferred
Authorization to work in the United States indefinitely without restriction or sponsorship
Position is full-time, working 8:00 AM-5:00 PM Monday-Friday. Candidates currently living within commutable distance to Lancaster, PA are encouraged to apply.
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
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