Associate Project Manager

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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. Eurofins 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. The Group also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Role Overview

The GMP Testing Project Manager is responsible for planning, coordinating, and overseeing Good Manufacturing Practice (GMP)-compliant testing projects within a regulated laboratory environment. This role ensures timely delivery of testing services, adherence to regulatory standards (FDA, EMA, ICH), and effective communication with internal teams and external clients.

Key Responsibilities

• Project Management

Lead and manage multiple GMP testing projects from initiation to closure.

Serve as the primary point of contact for clients, ensuring clear communication and accurate interpretation of technical data across functional teams.

Work closely with the Business Development team to grow client relationship and revenue through cross selling and managing assigned projects to provide exemplary customer experience and value

Ensure testing activities comply with GMP, GLP, and relevant regulatory guidelines.

Collaborate with cross-functional teams (Operations, QA, Sample Registration, Pricing, Business Development).

Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or related field

Strong background in pharmaceutical sciences, analytical chemistry, or biologics.

Knowledge of GMP regulations (21 CFR Part 210 / 211, EU GMP).

Position is full-time, Monday-Friday, 8 : 00 a.m.-4 : 00 p.m. with additional hours, as needed. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.

We offer excellent full-time benefits including :

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.