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Job Description
Company DescriptionEurofins 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.
In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.
Job DescriptionThe Extractables & Leachables Testing department evaluates container closure systems, delivery systems, manufacturing components, and medical devices for extractable and leachable compounds that may pose health risks to the patient.
This individual will:
Perform various tasks and analyses of Bio/pharmaceutical ingredients and products with a high degree of accuracy and precisionReview/prepare standards and samples for analysis and running a variety of equipment or instrumentation independentlyTroubleshoot and solve instrumental and/or method problemsWork efficiently, proactively, and productively Ensure that client receives quality data by reviewing laboratory data for accuracy, clarity and adherence to GMP and/or GLP regulations;Evaluate current systems and suggest process improvements when appropriate;Write complete and detailed investigations independently;Support multiple projects simultaneously;Demonstrate leadership qualities and train newer analysts.
QualificationsMinimum Qualifications:
Bachelor's degree in chemistry, biology, biochemistry, or related degree concentrationAuthorization to work in the US indefinitely without restriction or sponsorship2 years of GMP laboratory experience1 year of experience with GC/MS in industry
Preferred Qualifications:
Experience operating GC/MS and/or ICP systems. Experience with extractables and leachables testingExperience with ISO 10993 and/or
ISO 18562
testingExperience in a cGMP, GLP, and/or
ISO 17025
compliant/accredited lab. Experience with method development and validationExperience identifying unknown compounds by mass spec. Polymeric experience/educationAdditional InformationWorking schedule will be Full-Time, M-F 8am-5pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. No relocation assistance will be given. 25% travel may be required. This position is NOT remote. What we
Offer:
Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.