Eurofins is the world leader in the bio/pharmaceutical testing market. With over €5.3 billion in annual revenues and 55,000 employees across 900 sites in 50 countries, Eurofins is a leading international group of laboratories providing an unparalleled range of testing and support services to the pharmaceutical, biopharmaceutical, food, environmental, and consumer products industries and to governments.
The Eurofins BioPharma Product Testing (BPT) Group is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide. Eurofins BPT provides comprehensive CMC laboratory services for the world’s largest pharmaceutical and biopharmaceutical companies. The service portfolio supports all stages of the drug development process and all functional areas of bio/pharmaceutical manufacturing, including method development, microbiology, process validation and quality control.
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 method development and/or method validation.
The Ideal Candidate would possess:
Minimum Qualifications:
The position is full-time, Monday-Friday, 8am-4pm, with overtime as needed. Candidates within a commutable distance of Lancaster, PA are encouraged to apply.
Eurofins USA BioPharma Services is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
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If you're a dedicated and skilled individual looking for an exciting opportunity in method development, Eurofins is eager to welcome a Senior Scientist into our Small Molecule Method Development and Validation team based in Lancaster, Pennsylvania. At Eurofins, we take pride in being the world leader in the bio/pharmaceutical testing market, maintaining a steadfast commitment to quality while offering a vibrant workplace to our 55,000 employees. In this role, you will be at the forefront of method validations, transfers, and verifications for active pharmaceutical ingredients (APIs) and finished products. Your expertise in HPLC, GC, UV/Vis, and dissolution will be put to great use as you perform a broad range of analytical tasks critical to drug testing. The position also offers the chance to mentor junior staff and manage client projects, making it a perfect fit for someone who thrives in a collaborative environment. If you have 3-5 years of experience in a GMP context and a background in analytical chemistry, we’d love to see you bring your positive attitude and attention to detail to our innovative team. Don’t miss out on this chance to grow within a company dedicated to development and excellence in the pharmaceuticals sector together with Eurofins!
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