*THIS IS NOT A DATA SCIENCE POSITION*

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 Organisation 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 Organisations. It also has a rapidly developing presence in highly specialised 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 decentralised 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.

*THIS IS NOT A DATA SCIENCE POSITION*

Job Summary: Eurofins BPT Small Molecule Method Development and Validation is seeking a Data Review Scientist II to join their team in reviewing batch records and ensuring cGMP quality standards are met.

• Determine if data is compliant and defendable based on industry regulations and methodology
• Verify scientific data is of sound quality following all method, industry, and client requirements where applicable
• Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations
• Review simple and complex routine and non-routine data (for three or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; ensure all work is performed according to GLP/GMP requirements and apply GLP/GMP in all areas of responsibility as appropriate
• Diagnose problems, solve simple problems, and suggest solutions to complex problems in professional area
• Review methods to ensure procedures are followed
• Authorize written reports (e.g., SOP, OMC, client reports)
• Other job duties as required

The Ideal Candidate would possess:

• Strong scientific and organizational skills
• Strong attention to detail
• Previous experience with LIMS preferred 
• Previous experience with Excel
• 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

Minimum Qualifications:

• Bachelor's degree in chemistry, mathematics, physics, or other related degree concentration, or equivalent directly-related experience
• 3 years of experience in a cGMP environment
• Authorization to work in the United States indefinitely without restriction or sponsorship

Position is full-time position, Monday - Friday 8:00am - 4pm. 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

To learn more about Eurofins, please explore our website www.eurofinsus.com.

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