Eurofins

Global lab testing and analytics network

Analytical Chemist - Method Development & Validation

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeLancaster, PA, USANo salary listed

About the Job

Requirements

A BS with at least 4 years of industry experience, an MS with at least 2 years of industry experience, or a PhD with at least 1 year of industry experience is required.
At least 3 years of industry experience with chromatography is required.
At least 3 years of experience with liquid chromatography validation in a good manufacturing practice environment is required.
Authorization to work indefinitely in the United States without restriction or sponsorship is required.
Ability to communicate orally and in writing, with attention to detail, is required.
Ability to work independently and as part of a team is required.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies is required.

Responsibilities

Apply good manufacturing practices in all areas of responsibility, as appropriate.
Perform analytical tasks to validate analytical methods used in testing drug products and raw materials, including high-performance liquid chromatography, gas chromatography, ultraviolet/visible spectroscopy, and dissolution procedures.
Read, understand, and interpret diverse analytical procedures.
Conduct analytical investigations.
Troubleshoot instrumentation and communicate with vendors when required.
Train and mentor junior staff in laboratory procedures.
Manage and discuss projects with clients.

Desired Qualifications

Excellent communication (oral and written) and attention to detail.
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.

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.

Applies GMP in all areas of responsibility, as appropriate.
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.
Reading, understanding, and interpreting diverse analytical procedures.
Conducting analytical investigations.
Troubleshoot instrumentation and communicate with vendors when required.
Train and mentor junior staff in laboratory procedures.
Manage and discuss projects with clients.

Qualifications

Minimum Qualifications:

BS or MS degree in analytical chemistry or other related degree concentration.
BS and 4+ years of industry experience, MS and 2+ years of industry experience, or PhD and 1+ year of industry experience.
3+ years of industry experience with chromatography
3+ years of experience with LC chromatographic validation in a GMP environment.
Authorization to work in the U.S. indefinitely without restriction or sponsorship

The Ideal Candidate would possess:

Excellent communication (oral and written) and attention to detail.
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

Additional Information

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.

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size: 10,001+
Company stage: IPO
Headquarters: Luxembourg
Founded: 1987

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