CVP Quality Partner
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Kalundborg
Looking for an exciting role in pharmaceutical manufacturing? Join our team at PS API Manufacturing Development! As part of the API Manufacturing Development Business Support department, you'll work alongside skilled colleagues in Bagsværd and Kalundborg, supporting manufacturing operations. Take on key responsibilities in Analytical Support and Process Support, contributing to late-phase development, process optimization, and quality control. Don't miss this opportunity for growth and development in a dynamic and impactful role. Apply now and be part of our mission to improve lives through high-quality pharmaceuticals. The Position PS API Manufacturing Development is situated in both Bagsværd and Kalundborg. You will be part of the API Manufacturing Development Business Support department and will be part of a team with highly skilled colleagues supporting Manufacturing Development. The main responsibility lies within the two biggest departments: Analytical Support and Process Support. Analytical support is responsible for the late-phase development and validation of analytical methods for new products, prior to transfer to QC departments. Process Support is responsible for process support and optimization for Novo Nordisk's API production of Diabetes. Lastly, the departments play a crucial role in supporting the production and Quality control laboratories. The Job Entails That You Work out of Bagsværd and Kalundborg, providing support for quality activities across Manufacturing Development, ensuring the appropriate level of compliance. These activities will span different quality levels, such as GSP and GMP Take responsibility for preparing and coordinating internal audits and inspections involving API Manufacturing Development Drive optimization, automation, and digitalization initiatives within the two departments acting as a challenger and collaborator with initiative owners to ensure the right level of quality—neither excessive nor insufficient. Be an integral part of the Quality Partner organization in PS API, supporting alignment and quality activities within the department. Support daily business operations related to quality, working alongside the departments and QA to ensure the appropriate level of quality is maintained. Qualifications To succeed in the role, we expect that you have Relevant degree in engineering, or another scientific background with an interest in data Deep understanding of GMP and quality in production and analytical laboratories from years of relevant experience in the Pharma industry Strong analytical mindset, holistic perspective on business processes, and ability to see what is important, and what is not Experience with project management in order to drive projects across MDev in collaboration with relevant colleagues and stakeholders On a personal level, we expect you to be committed and show a high level of independence. We also expect that you are good at creating a clear overview and prioritizing your tasks; even when the deadline is approaching. You never compromise on quality and are also good at completing your tasks on time, then moving on to the next task with enthusiasm and energy. You have good communication skills and feel comfortable collaborating with people on all levels. All in all, we offer a very exciting job, with good development opportunities for the right candidate. About Novo Nordisk Novo Nordisk in Kalundborg is the world's largest insulin production site - big enough to have a 5.5 km run around the site and to produce half of the insulin used worldwide. This is a workplace for more than 3000 dedicated Novo Nordisk employees who set ambitious goals and strive to make a difference for our more than 24 million patients through stable deliveries of high-quality products. The site is in rapid development with lots of exciting challenges. We solve them by being at the forefront of technology, systems, methods, and processes, and by assembling teams of talented employees. In Novo Nordisk, it is your ability, your commitment, and your ambitions that help us improve the lives of many people. On the other hand, we offer you the opportunity to work with talented colleagues and we offer you a wide range of opportunities for professional and personal development. Contact Do you have any questions regarding the position or want to know more? Feel free to contact Sr. Manager Maria Gullander at +45 3075 1258 or Associate Manager Maria Tonsgaard at +45 3075 1548. Due to the holiday season, you might experience delay in responses. Deadline 6th August 2023. Applications will be reviewed on an ongoing basis, so we encourage you to apply as soon as possible. You are welcome to send your application in English or Danish. To ensure an efficient and fair recruitment process, please refrain from adding a photo to 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 in 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 the 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 28.2.2023, 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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| 6. oktober 2024 | 50 |