Pharmaceutical Product Quality Specialist

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.

Document receipt of stability samples and complete inventories. Appropriately handle documentation. Understand stability requirements - protocols, LIMS, storage chamber conditions, labeling of samples and storage positions. Provide support for project managers and laboratory staff. Compose business appropriate communication (i.e. e-mail, document) for client or internal use.

Essential Duties and Responsibilities :

• Applies GMP / GLP in all areas of responsibility, as appropriate
• Demonstrates and promotes the company vision
• Regular attendance and punctuality
• Applies quality to all areas of responsibility, understands and promotes quality culture.
• Understand and update LIMS appropriately for protocol and sample activities.
• Manage inventory for incoming project samples; set up stability studies, label samples, and place into chambers.
• Verify sample chamber placement, labeling, container counts, and LIMS entry
• Pull samples from chambers at appropriate intervals; perform periodic chamber inventories
• Maintain contents of stability chambers in an organized manner, monitor and change charts; clean inside of chambers
• Follow all department procedures and SOPs; understand and apply GMP / GLP regulations to daily work; document data according to regulatory requirements
• Attend department meetings
• Independently evaluate and / or provide shipment paperwork, package samples for shipment as needed with additional training.
• Effectively use word, tone, body language to share and receive information.
• Accept and implement process change to support business goals.
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Minimum Qualifications :

Working schedule will be Full-Time, First Shift, M-F 9am-5pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. No relocation assistance will be given. This position is NOT remote.

What we Offer :

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