Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing.

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 specialised 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.

To perform this job successfully, the individual must be able to independently perform the following requirements below. 

• Support client driven audits and author audit response reports
• Technical writing and review
• Tracking action items and driving to completion
• Ability to identify trends in recurring events
• Batch record review, pharmaceutical testing and room clearance activities
• Ensure quality of operations and data being produced in the laboratories
• Ensure laboratory adherence to government regulations and client requirements

The ideal candidate would possess:

• To perform this job successfully, the individual must be able to independently perform the following requirements below.
• Support regulatory agency audits and response reports Investigation writing and review, including thorough root cause analysis
• Ability to work in a fast paced environment
• Excellent communication skills
• Knowledge in Data Integrity and the Change Control process.
• Computer skills including word processing, spreadsheets, power point, and database is also helpful
• Experience in regulatory compliance is preferred
• Experience with cGMP and/or FDA regulated environment a plus.
• Bachelor's degree in biology or related science preferred
• Authorization to work in the United States indefinitely without restriction or sponsorship

Position is Full Time, Monday-Friday, 8:00 a.m.-5:00 p.m., with additional hours, as needed.  Candidates currently living in a commutable distance to Lancaster, PA are encourage to apply. 

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