Operational Responsible to Automatic Visual Inspection
Denne stilling er desværre ikke længere ledig.
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Kalundborg
Would you like to be part of ensuring that we can release our medicine in a way that meets all applicable regulatory requirements and guidelines, and that we are always ready for inspection? Do you dream of expanding your experience with inspection machines? Then you might be our new Operational Responsible! Read more and apply today. The Position As a Operational Responsible to Automatic Visual Inspection (AVI), you will be part of a team consisting of skilled and motivated employees who look forward to meeting you. In this position we work with many different professional groups, internal and external stakeholders where you will be responsible for the process of our automatic visual inspection machine. Your main focus will be on: Development and implementation of new processes.
Establishment and approval of new procedures.
A wide range of other quality-related tasks, like updating and innovating our procedures to make them even more robust in the future.
Qualifications The qualifications we value include having: A bachelor’s degree in mechanical engineering, production engineering, marine engineering or similar.
Experience with inspection or production machines from the pharma industry and knowledge of GMP.
Experience with validation is considered a plus.
Experience with writing and reading documents in Danish and English.
Fluency in English and Danish.
On a personal level, you are curious to learn and work with our Process Automation System. While being administratively strong, you proud yourself in having exceptional skills for creating and maintaining an overview of many different data. Our new colleague will enjoy working with optimization and validation tasks and thrive on thinking about innovative solutions that can improve the quality of operations and processes. Having great communication skills and stakeholder management skills are key to succeed in this role. About the department Biotech and rare disease (BRD) is part of Novo Nordisk Product Supply, which produces our life-changing medicines at five production sites in Denmark and the USA – together, we cover the entire production value chain, where raw materials are grown, purified, formulated, filled, assembled into units, packaged, and distributed worldwide. At the factory in Kalundborg, we fill BRD products, e.g., for patients with conditions such as growth disorders or hemophilia, and package them to comply with all applicable regulatory requirements and guidelines. In Inspection & Release Support, we ensure, in collaboration with production, that we release batches to our customers daily while continuously improving the process and optimizing the flow. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Tommy Bennet Busk at +45 3448 2246, Kim Steffensen Flugt at +45 3448 9672. Deadline Apply before March, 17 2024. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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 26.2.2024, 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 |