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Full Time Method Validation Jobs in Pennsylvania

Frontage Laboratories

Associate Scientist

Exton, PA · On-site

... Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research ... The successful candidate will support bioanalytical method development, validation, and sample ...

Frontage Laboratories

Scientist Senior

Exton, PA · On-site

$88K - $120K/yr

Exton, PA Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract ... Conduct analytical method development and validation for drug substance and drug product. * Draft ...

Frontage Laboratories

Scientist

Exton, PA · On-site

Manager/Group Leader Full-time Location: Exton, PA Frontage Laboratories Inc. is an award winning ... The scientist's duties include analytical method development/method validation, protocol/report ...

Novocure

Digital Systems Validation Lead

Wayne, PA · Hybrid

$116K - $130K/yr

Digital Systems Validation Lead Chesterbrook, PA | Full-Time | Exempt At Novocure, we are patient ... Establish verification approaches, validation methods, and acceptance criteria, ensuring ...

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Infographic showing various Full Time Method Validation job openings in Pennsylvania as of August 2026, with employment types broken down into 89% Full Time, 3% Part Time, and 8% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution.

Analytical Chemist- Method Development & Validation

Eurofins Scientific

Lancaster, PA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted just now

Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

68th of 120 rated laboratories

Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.

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.

What Eurofins employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US

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