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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 50,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.

In 2020, Eurofins generated total revenues of EUR 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Reference Material Scientist responsibilities include, but are not limited to, the following:

Inventory and Distribution

Monitor the Reference Material and Critical Reagents Database and inventoryReceive and ship Reference Materials and Critical Reagents (distribution onsite and globally)Fill/Finish onsite batches of Reference Materials and Critical Reagents

Material Qualification and Lifecycle Management

Perform sample testing, as needed (A280, DRID, Dot Blot, and other analytical testing)Write protocols, reports, and CofAs for Reference Materials and Critical ReagentsCoordinate testing at various sites for reagent qualification or requalification

General

Manage multiple projects based on priorityComply with FDA, EPA, DEP, DOT, OSHA, and client regulations and policies, as well as complete all required training by due datesProvide superlative service to clients by performing duties accurately and within the expected timeframe under minimal supervision following GMPDocument work accurately, clearly, and in compliance with client’s requirements

Qualifications

The ideal candidate would possess:

Strong computer, scientific, and organizational skillsExcellent communication (oral and written) and attention to detailAbility to work independently and as part of a team, self-motivation, adaptability, and a positive attitudeAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesA strong understanding of analytical methodsAt least 2 years of technical writing related to the pharmaceutical industry and relevant experience reviewing and trending data

Basic Minimum Qualifications:

Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)Familiarity with GMP/GLP1-2 years of relevant experienceAuthorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of Malvern, PA are encouraged to apply.

Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidays

 

 

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.