Principal Scientist, Small Molecule Method Development and Validation

Eurofins USA; Lancaster (Lancaster County); On-site; USD 80,000 - 110,000; Full time

Job summary

A leading company in bio/pharmaceutical testing is seeking a Principal Scientist for method development and validation. The role involves performing validations, transfers, and verifications on APIs and finished products. The ideal candidate will have experience in a GMP environment and strong analytical skills. Benefits include comprehensive insurance and a 401(k) plan.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

401(k) with company match

Paid vacation

Paid holidays

Qualifications

• 3-5 years of experience with LC chromatographic validation in a GMP environment.
• Excellent communication skills and attention to detail.

Responsibilities

• Perform analytical tasks related to method validation of drug testing procedures.
• Train and mentor junior staff.
• Manage and discuss projects with clients.

Skills

Communication

Attention to Detail

Self-Motivation

Adaptability

Education

Higher education degree in analytical chemistry

BS with 4+ years

MS with 2+ years

PhD with 1+ years

Tools

HPLC

GC

UV/Vis

Dissolution

Job description

Principal Scientist, Small Molecule Method Development and Validation

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 provides an extensive range of testing and support services to the pharmaceutical, biopharmaceutical, food, environmental, and consumer products industries, as well as to governments.

The Eurofins BioPharma Product Testing (BPT) Group is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide. Eurofins BPT offers comprehensive CMC laboratory services to the world’s largest pharmaceutical and biopharmaceutical companies, supporting all stages of drug development and manufacturing, including method development, microbiology, process validation, and quality control.

Job Summary: Eurofins Small Molecule Method Establishment is seeking a Senior Scientist responsible for performing method validations, transfers, and verifications on APIs and finished products. Candidates should have expertise in method development and/or validation.

• Apply GMP principles in all responsibilities.
• Perform analytical tasks related to method validation of drug testing procedures, including HPLC, GC, UV/Vis, and dissolution.
• Interpret diverse analytical procedures.
• Conduct analytical investigations and troubleshoot instrumentation issues, communicating with vendors as needed.
• Train and mentor junior staff.
• Manage and discuss projects with clients.

The Ideal Candidate would possess:

• 3-5 years of experience with LC chromatographic validation in a GMP environment.
• Excellent communication skills (oral and written) and attention to detail.
• Ability to work independently and collaboratively, with self-motivation and adaptability.
• Willingness to learn new techniques, perform multiple tasks, maintain accurate records, and follow company policies.

Minimum Qualifications:

• Higher education degree in analytical chemistry or related field.
• BS with 4+ years, MS with 2+ years, or PhD with 1+ years of relevant experience.
• Authorization to work in the U.S. without restrictions or sponsorship.

The position is full-time, Monday-Friday, 8 am-4 pm, with overtime as needed. Candidates within commuting distance of Lancaster, PA are encouraged to apply.

• Benefits include medical, dental, vision, life and disability insurance, 401(k) with company match, paid vacation and holidays.

Eurofins USA BioPharma Services is an Equal Employment Opportunity employer, supporting Disabled and Veteran applicants.