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 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.

Job DescriptionFunction as an MS subject matter expert within Analytical Development and be viewed as peer to other MS SMEs within Eurofins networkPerform method development, feasibility, qualification and/or validation of methods in support of biopharmaceutical products using primarily Mass spectrometryExecute identification of unknown compounds with minimal supportDevelop and execute validation plansTroubleshoot method and instrumentation problemsGenerate complete, accurate, and concise documentation using electronic systems and laboratory notebookAuthor documents (e.g., development reports, methods and client reports)Give presentations for training and client reviewsHave a strong understanding of current regulatory expectationEffectively guide more junior scientists on technical issuesUse office and instrumentation specific computer softwareContribute to set up an oligonucleotide testing laboratory and establish processes, workflows and general operationsDeveloping and validating new QC methods to assess the suitability, stability, and functionality of a range of oligonucleotides through a variety of analytical and functional testsHPLC and high resolution mass spectrometry method development for oligonucleotide characterizationInstallation and verification of equipment, documenting processes, and training operatorsSupport various analytical instrument operation, maintenance and troubleshooting to sustain analytical performance, data reproducibility and reliability to deliver results to project teams within a timely mannerChampion and implement new and innovative analytical applications and technologyAdvise clients on analytical scope to meet technical and regulatory requirementsHandling any customer related queries where necessary and liaising with the team to problem solve these queries if neededProvide training/mentoring to junior staff

QualificationsB.S. / M.S. degree in Chemistry, Biology, biochemistry or related technical discipline with 4+ years of relevant experience, either post-doctoral or in the bio/pharmaceutical industryHands-on experience in use of multiple types of mass spectrometers (GC/MS, LC/MS, HRMS)Experience with identification of unknown materialsAbility to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude.Strong organizational and time management skillsExcellent communication (oral and written) and attention to detailAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesAuthorization to work in the United States indefinitely without restriction or sponsorship.Extensive knowledge of oligonucleotide based drug products including ASO, siRNA, mRNASubject matter expert analytical chemistry knowledge including theory and application of three or more chromatographic and spectroscopic techniques for identification, purity, and assay of various analytesOperate and troubleshoot available instruments including HPLC and MSExperience with an assortment of different HPLC separations which includes IEX, RP, SEC, etc.Hands-on experience in QC of oligonucleotides

Additional Information

Position is full-time position, Monday - Friday 8:00am - 4:00pm. Candidates currently living within a commutable distance of Lancaster, 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

To learn more about Eurofins, please explore our website www.eurofinsus.com.

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