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.

Job Description

 

Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, aerosols, liquids, creams, and gels)Run the instrumentation independently including, but not limited to, various chromatographic systems, {NAME} (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatusPrepare samples for analysis and run some instrumentation with minimum supervisionSet up and validate new analytical or related processes used by the departmentPrepare standards and samples for analysisExecute method transfer protocolsDocument work as required for GMP compliancePerform monthly maintenance of laboratory equipmentDevelop and optimize analytical methods for the quantification of pharmaceutical compounds and their impuritiesCollaborate with cross-functional teams to support drug development projects and ensure analytical method suitabilityTroubleshoot and resolve analytical issues related to method development and validationParticipate in the writing and reviewing of Standard Operating Procedures (SOPs) and analytical reportsAssist in the training of junior scientists on analytical techniques and instrument operationStay current with relevant scientific literature and regulatory guidelines in the field of pharmaceutical analysisContribute to continuous improvement initiatives within the laboratory to enhance efficiency and data quality

 

QualificationsStrong 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 policies

Minimum Qualifications:

Bachelor's degree in chemistry or other related degree concentration, or equivalent directly-related experienceAuthorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with additional hours as needed as workloads demand. 

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

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.