Senior Scientist, Small Molecule Method Validation

Eurofins US; Lancaster (Lancaster County); On-site; USD 80,000 - 100,000; Full time

Job summary

A leading company in bio/pharmaceutical testing is seeking a Senior Scientist for method validation and development. The role involves performing analytical tasks, training junior staff, and managing projects with clients. Ideal candidates will have a strong background in analytical chemistry and experience in a GMP environment.

Benefits

Comprehensive medical, dental, and vision coverage

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Qualifications

• 3-5 years of experience with LC chromatographic validation in a GMP environment.
• Ability to work independently and collaboratively.

Responsibilities

• Perform method validations, transfers, and verifications on APIs and finished products.
• Train and mentor junior staff in laboratory procedures.

Skills

Communication

Attention to Detail

Adaptability

Education

Higher education degree in analytical chemistry

BS

MS

PhD

Tools

HPLC

GC

UV/Vis

Dissolution

Job description

Senior 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 unparalleled 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 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 to perform method validations, transfers, and verifications on APIs and finished products. Candidates should have expertise in method development and/or validation.

• Apply GMP in all responsibilities as appropriate.
• Perform analytical tasks for validating methods used in testing drug products and raw materials, including procedures like HPLC, GC, UV/Vis, and dissolution.
• Read, interpret, and understand diverse analytical procedures.
• Conduct analytical investigations and troubleshoot instrumentation issues, liaising with vendors when needed.
• Train and mentor junior staff in laboratory procedures.
• 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, adaptability, and a positive attitude.
• Capacity to learn new techniques, handle multiple tasks, maintain accurate records, follow instructions, and adhere to 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 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 comprehensive medical, dental, and vision coverage.
• 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.