Job DescriptionJob DescriptionCompany 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, , composition, authenticity, , traceability and purity of biological substances and products.
Job Description
Function as an MS subject matter expert within Analytical Development and be viewed as peer to other MS SMEs within Eurofins network
Perform method development, feasibility, qualification and/or validation of methods in support of biopharmaceutical products using primarily Mass spectrometry
Execute identification of unknown compounds with minimal support
Develop and execute validation plans
Troubleshoot method and instrumentation problems
Generate complete, accurate, and concise documentation using electronic systems and laboratory notebook
Author documents (e.g., development reports, methods and client reports)
Give presentations for training and client reviews
Have a strong understanding of current regulatory expectation
Effectively guide more junior scientists on technical issues
Use office and instrumentation specific computer software
Contribute to set up an oligonucleotide testing laboratory and establish processes, workflows and general operations
Developing and validating new QC methods to assess the suitability, stability, and functionality of a range of oligonucleotides through a variety of analytical and functional tests
HPLC and high resolution mass spectrometry method development for oligonucleotide characterization
Installation and verification of equipment, documenting processes, and training operators
Support various analytical instrument operation, maintenance and troubleshooting to sustain analytical performance, data reproducibility and reliability to deliver results to project teams within a timely manner
Champion and implement new and innovative analytical applications and technology
Advise clients on analytical scope to meet technical and regulatory requirements
Handling any customer related queries where necessary and liaising with the team to problem solve these queries if needed
Provide training/mentoring to junior staff
Qualifications
B.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 industry
Hands-on experience in use of multiple types of mass spectrometers (GC/MS, LC/MS, HRMS)
Experience with identification of unknown materials
Ability 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 skills
Excellent communication (oral and written) and attention to detail
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Authorization to work in the United States indefinitely without restriction or sponsorship.
Extensive knowledge of oligonucleotide based drug products including ASO, siRNA, mRNA
Subject matter expert analytical chemistry knowledge including theory and application of three or more chromatographic and spectroscopic techniques for identification, purity, and assay of various analytes
Operate and troubleshoot available instruments including HPLC and MS
Experience 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 options
Life and insurance
401(k) with company match
Paid vacation and holidays
To learn more about Eurofins, please explore our websitewww.eurofinsus.com.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
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