Quick overview
Job description
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.
2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.
Management of pharmaceutical microbiology testing (routine and non-routine):
Coordinates sample collection, data entry, and team operations for environmental and utility monitoring programs in cleanrooms, laboratories, and or industrial settings.
Apply GMP/GLP principles and maintain the highest quality standards in all areas of responsibility
- Ensure the quality policy program is understood, implemented, and maintained; identify and correct any departures from the quality system
- Supervise assigned employees in performing work and meeting client requirements; coordinate workflow and monitor daily operations to meet turnaround times
- Conduct semi-annual performance reviews, interview applicants, maintain training records, and develop succession plans for assigned employees
- Coach, train, and develop team members to maximize performance and support effective implementation of operational improvements
- Develop and implement operational improvements; continually evaluate systems and processes to enhance productivity and quality
- Demonstrate strong technical knowledge of instrumental and analytical theory; troubleshoot and resolve technical and method issues
- Communicate effectively with client staff members and support the writing of investigations to strengthen technical documentation
- Monitor and approve employee time entries; address performance issues and foster team motivation and morale
- Expand leadership skills through applicable training; perform all functions in compliance with state and federal employment regulations and safety requirements
- Perform additional duties as assigned to ensure smooth department operations
- Bachelor's degree in chemistry, biology, biochemistry, or related degree concentration and at least 3 years of laboratory experience
- Experience in conducting laboratory investigations and supporting audit responses
- Authorization to work in the United States indefinitely without restriction or sponsorship.
This is a full-time position, working Monday-Friday 8am-5pm, overtime as needed. Candidates currently living within commutable distance to Indianapolis, IN 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 Disabled and Veteran Equal Employment Opportunity employer.
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