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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, 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 in the support of clinical studies.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. 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, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Lead a large team executing multiple QC functions in a pharmaceutical manufacturing environment.

• Excellent knowledge of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs) on a daily basis.
• Good understanding of general Microbiology techniques such as gram staining; filtration testing, microbial identification, aseptic technique, and plate streaking techniques.
• Knowledge of USP and other regulatory requirements.
• Excellent attention to detail and problem solving skills.
• Outstanding organizational skills and ability to lead in a team environment
• Strong knowledge of pharmaceutical manufacturing regulatory process including the execution of investigations, deviations, and CAPA
• Strong verbal, written, and interpersonal communication skills are require

• 3-4 years of relevant experience in a GMP-regulated environment including leadership experience and a BS or higher in Microbiology, or degree in related fields

Position is full-time, 5 days per week, 8 hours per day, Monday - Friday, Hours: 10:00 am – 6 pm. Candidates currently living within a commutable distance of Frederick, MD 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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.