Bioassay Data Review Specialist

About the role

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.

Responsibilities

• Applies GMP/GLP in all areas of responsibility, as appropriate.
• Perform verification of data and confirm resolution of issues identified
• Anticipate quality events or issues and elevate them to appropriate management attention immediately
• Independently engage and collaborate with coworkers, customers, and management within a cGMP environment
• Must be able to identify problems and know when to solve proactively and seek advice
• Contribute and participate in investigations, as needed
• Support regulatory and client inspections, as needed

Qualifications

• Proficiency in cGMP and FDA-regulated clinical services laboratory environment
• Strong computer, scientific, and organizational skills
• Excellent written and oral communication with attention to detail
• Capability to work well on a team and be able to troubleshoot and problem-solve in cross-functional team setting
• Ability to read, comprehend, and present complex subjects

Bachelor's degree in biology, biochemistry, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)

At least 3 years of related GMP pharmaceutical experience in either an operations or testing role

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

Benefits

• 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

Schedule

Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as needed

Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply.