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Merck is a leading science and technology company in healthcare, life science and performance materials. Around 50,000 employees in 67 countries work to further develop technologies that improve and enhance life – from biopharmaceutical therapies to treat cancer or multiple sclerosis, cutting-edge systems for scientific research and production, to liquid crystals for smartphones and LCD televisions.
As Process Validation Engineer, you ensure the manufacturing of both Clinical Trials and Process Validation batches according to the Good Manufacturing Practices and Company’s Quality Standards. You elaborate the process validation and the Technology Transfer protocols and reports for both Clinical Trials phase III and submission batches to allow the registration of the drug products within the expected timelines. Finally, you ensure backup site readiness plan for commercial products.
What we offer:Your possibilities to develop in our growing company are just as manifold as our product portfolio. We offer a modern and international working environment to unleash your innovative potential in diverse teams, and take responsibility for our employees, products, the environment and society.
Curious? Apply and find more information at come2merck.com