Stability Specialist I

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.

• 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

• College degree in related field strongly preferred or High school diploma with 1+ year experience 

• Authorization to work in the United States indefinitely without restriction or sponsorship

Position is full-time, Monday - Friday 6:00am - 2:00pm . Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.

• 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 M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.