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.

• Execute sample receipt, processing, and aliquoting to support in-process testing, release testing, stability, or retains.
• Collaborate with other departments (Quality Control, Quality Assurance and Manufacturing) to support requirements for release testing, stability or retains.
• Perform routine review of records including, but not limited to, sample chain of custody, sample processing, logbooks, and other documentation generated.
• Performs routine and non-routine inspection of media fill samples (AOQ/APV), In-Process environmental monitoring, final product, validation-related, and critical utility samples according to SOPs.
• Handle bio-hazardous waste and coordinates its removal with qualified safety personnel.
• Perform routine laboratory maintenance per the SOPs
• Routine cleaning of laboratory equipment: Biosafety Cabinets, Centrifuge, Freezers & Incubators
• Complete required training assignments to maintain necessary technical skills and knowledge, and to ensure compliance with cGMP requirements.
• Supervising a team of analysts while performing client’s service requirement.
• Coach, train, and develop others within the group with respect to their personal development and effective implementation of operational procedures.

• 1-2 years of relevant experience in a GMP-regulated environment and a BS degree, or degree in related field

Preferred Requirements:

• Prior experience in biopharmaceutical or pharmaceutical industry
• Prior lab experience
• Basic Knowledge of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs) on a daily basis.
• Knowledge of USP and other regulatory requirements.
• Proficiency in Microsoft Office applications
• Ability to work effectively in a team environment.
• Strong verbal, written, and interpersonal communication skills are required.
• MODAL/LIMS proficiency.
• Leadership exposure

Position is full-time. The work schedule will be 4 days per week, 10 hours per day, Sunday through Wednesday or Wednesday through Saturday. Hours: 7:00am – 6:00pm for first shift, and 3:00pm – 2:00am for third shift. Candidates must be flexible to adapt to schedule changes requiring shift changes and/or weekend work, and overtime may be required as needed. 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.