Senior Cleaning Validation CIP Scientist
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Kalundborg
Would you like to join a dynamic global company and work on an exciting new capacity expansion project? Are you interested in the opportunity to establish new active pharmaceutical ingredients (API) manufacturing facilities that bridges new and automated technologies with strong know-how and expertise in biotech manufacturing? Then join us as our new Senior Cleaning Validation CIP Scientist and be a part of our expanding team! Don't miss this opportunity. Submit your application today! We are hiring experienced colleagues to join the investment project. The position Novo Nordisk has announced plans to invest more than DKK42 billion to expand existing manufacturing facilities in Kalundborg, to support the current and future company portfolio within serious chronic diseases. As a Senior Cleaning Validation Process Scientist,you will participate in project activities for investigating design, constructability, schedule and cost for a new purification facility. The key design principle will be to implement the best-in-class design standards from other facilities. You can look forward to working with the following tasks: Participate in project activities such as design review, design risk assessments, FAT and SAT Test and documentation Validation of CIP (Cleaning-in-Place) of all process equipment, including ownership of CIP specific processes. Stakeholder management You will take an active part in a competent user organisation, integrating with engineering partners, and collaborating with contractors while supervising their activities, while managing project risks proactively and developing standards to ensure structure and transparency. Furthermore, we expect you to help us keep the team focused on implementing known solutions as well as developing new design solutions where relevant. We are open to adjusting the tasks and the level of the position to your experience. The activities will be carried out at our site in Kalundborg, Novo Nordisk hub for API manufacturing. Qualifications To be successful in this role, we imagine that you have: +6 years experience within Good Manufacturing Practice and ideally Active Pharmaceutical Ingredient manufacturing. Minimum a bachelor’s level education in in Natural Sciences, engineering or similar. A solid understanding of unit operations, pharmaceutical processes and documentation. Full professional English proficiency (verbal and written). It would be advantageous if you have knowledge and experience related to design review and validation of CIP On a personal level, you will thrive in this job if you enjoy close teamwork, can ride out a storm, and are a motivator for others. You thrive in a multicultural environment that demands independence to make critical decisions. Building structure comes naturally to you and you strive for simplicity. You are motivated to succeed and have the desire to set a very clear direction. About the department We are a rapidly growing purification department in Novo Nordisk API expansion area. We are designing and validating a new purification facility, together with numerous stakeholders. Our approach is innovative, stakeholder focused, and inclusive in everything we do. You will be part of a department with experienced and dedicated colleagues, where we take pride in collaboration, so we get access to all the knowledge and know-how that everyone in the team possesses. Working at Novo Nordisk Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat serious chronic diseases, built upon our heritage in diabetes. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 61,400 people in 80 countries and markets its products in around 170 countries. About Novo Nordisk Kalundborg Since 1969, Novo Nordisk Kalundborg has been a cornerstone in our production of API. With more than 50 years of expertise in large-scale biotech manufacturing, we are today the world’s largest insulin-producing facility. Our 4,400 employees at Novo Nordisk Kalundborg produce half of the world’s insulin, and a number of biopharmaceutical products. Together, we make a difference every day for more than 35 million people living with diabetes and other chronic diseases. Join our growing manufacturing hub in Kalundborg and gain thousands of dedicated colleagues. It is your drive and our passion, that makes a difference for their future. Are you ready for a life-changing career? Contact For further information, please contact Senior Project manager Trine Dissing Bøgh Olesen at +45 30777356. Deadline 15 December 2023. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Kalundborg.
Jobbet er oprettet på vores service den 13.11.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Kalundborg
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Statistik over udbudte øvrige i Kalundborg over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 2. juli 2024 | 38 |
| 1. juli 2024 | 39 |
| 30. juni 2024 | 50 |
| 29. juni 2024 | 51 |
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| 7. juni 2024 | 58 |
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| 5. juni 2024 | 55 |
| 4. juni 2024 | 57 |
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| 2. juni 2024 | 59 |