Company 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 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.
Job Description
Lead a department supporting multiple analytical and development functions in a pharmaceutical R&D environment both in a GMP and non-GMP environment.
Role requires leadership experience and a good understanding of analytical testing operations in a pharmaceutical R&D environment.
•Outstanding organizational skills and ability to build and lead a strong team in a diverse environment
•Excellent attention to detail and problem solving skills. Ability to design and change work streams in organization
•Strong knowledge of pharmaceutical manufacturing regulatory and R&D process
• Good understanding of regulatory frameworks in the pharmaceutical sector including GMP and USP
•Strong verbal, written, and interpersonal communication skills are require
Qualifications
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