Merck Gruppe
Work Your Magic with us Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. Your role: As member of the Quality Assurance group you will bring your support to validation of standard laboratory equipment, training of employee by supporting the administrator of HR4You learning system in training matrix definition and management, ticketing system, documentation management by writing, reviewing, and approving Operating Procedures, Reports, Protocols and other QC controlled documents. You will ensure: compliance of local Pharmaceutical Quality System with Merck Quality standards by ensuring that all documents are communicated and timely implemented across the site and also continuous improvement and performance management by monitoring quality KPI, issuing periodic reports and calculating quality index metrics. You will take part in discussion and actively participate to the continuous improvement of the team and to the daily activities of the QA System. Who you are: University degree (min Bachelor) in scientific education ( pharmacy, pharmaceutical chemistry, biochemistry, chemistry) At least 3 years in pharmaceutical industry and GMP environment Experience in Quality Systems management Methodic and well organized Fluent in English (written and spoken) Knowledge in analytical equipment validation is a nice to have What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress Apply now and become a part of our diverse team J-18808-Ljbffr
Per candidarti a questo lavoro visita www.adzuna.it.
