Job Description

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 Summary: Eurofins' BPT Small Molecule Method Development and Validation team is seeking an Scientist to join their team full time in Lancaster, PA. This individual will work in a duel analyst and data reviewer role. The Scientist will be able to:

• Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
• Execute specialized analyses and method transfer and feasibility testing
• Troubleshoot method and instrumentation problems
• Use office and instrumentation specific computer software
• Develop and execute validation plans
• Carry out method transfers and feasibility studies
• Train technical staff
• Some travel to client sites for technical meetings could be required
• Determine if data is compliant and defendable based on industry regulations and methodology
• Verify scientific data is of sound quality following all method, industry, and client requirements where applicable
• Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations
• Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate
• Diagnose problems, solve simple problems, and suggest solutions to complex problems in professional area
• Review methods to ensure procedures are followed
• Authorize written reports (e.g., SOP, OMC, client reports)

Qualifications

Minimum Qualifications:

• Bachelor's degree in chemistry, pharmaceutical science, or other related degree concentration and a minimum of 3 years of experience in a cGMP compliant industry lab.
• Master's degree in chemistry, pharmaceutical science, or other related degree concentration and a minimum of 1 year of experience in a cGMP compliant industry lab.
• Experience with HPLC and Empower
• Authorization to work in the U.S. without restriction or sponsorship

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 disability insurance
• 401(k) with company match
• Paid vacation and holidays

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

Job Tags

Full time, Contract work, Work at office, Monday to Friday,

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