Analytical Chemist- Method Development & Validation
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At a glance
Requirements
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Job overview
Eurofins Scientific is hiring an Analytical Chemist- Method Development & Validation. Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team is seeking candidates with expertise in Chromatography and method validation. This role applies GMP in all areas of responsibility and involves training junior staff and managing client projects.
Key focus areas include Apply GMP in all areas of responsibility, Perform analytical tasks for validation of analytical methods, and Read, understand, and interpret diverse analytical procedures.
Successful candidates bring BS Or MS In Analytical Chemistry, BS With 4+ Years Industry Experience, and MS With 2+ Years Industry Experience. Important skills include Chromatography, Method Validation, GMP, HPLC, GC, and UV/Vis. Preferred (not required): Collaboration.
Skills & qualifications
Skills
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Benefits
Full job description
Job Summary: Eurofins Small Molecule Method Establishment is seeking a Senior Scientist to perform method validations, method transfers, and method verification activities on APIs and finished products. The team is seeking candidates with expertise in Chromatography and method validation .
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Applies GMP in all areas of responsibility, as appropriate.
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Performing a large variety of analytical tasks for the validation of analytical methods used in the testing of drug products and raw materials by means of various procedures including HPLC, GC, UV/Vis, and dissolution.
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Reading, understanding, and interpreting diverse analytical procedures.
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Conducting analytical investigations.
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Troubleshoot instrumentation and communicate with vendors when required.
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Train and mentor junior staff in laboratory procedures.
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Manage and discuss projects with clients. Minimum Qualifications:
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BS or MS degree in analytical chemistry or other related degree concentration.
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BS and 4+ years of industry experience, MS and 2+ years of industry experience, or PhD and 1+ year of industry experience.
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3+ years of industry experience with chromatography
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3+ years of experience with LC chromatographic validation in a GMP environment.
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Authorization to work in the U.S. indefinitely without restriction or sponsorship The Ideal Candidate would possess:
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Excellent communication (oral and written) and attention to detail.
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Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
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Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Working schedule will be Full-Time, First Shift, Mon-Fri, 8am-4pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. 25% travel may be required. This position is NOT remote.
What we Offer:
- 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 Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
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