Associate Manager in CMC Development QA
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Måløv
Are you passionate about setting direction and ensuring timely delivery of development products to our patients in clinical trials? Are you motivated by developing both processes and people and continuously improving engagement and performance? Do you possess management experience, and would you like to be part of the growing business in CMC DP Development QA? If so, we have an exciting opportunity for utilising both professional and people skills. The position You will lead a team of 10-15 employees and refer to the Director in CMC DP QA. You will be a part of a department consisting of three teams where you will head up “Early Phase and CMO” where the main tasks in the team are supporting our aseptic pilot plant, releasing batches for early phase clinical trials internally produced as well as from external CMO collaborations. To be able to meet the new Annex 1 requirements for aseptic production there are different projects initiated and planned within the coming years to comply with the regulations. The major priority will be implementation of an isolator. As the department just last year went through an organisational change and we have welcomed several new colleagues, you will also have impact on establishing a new management group having a significant impact on the future strategic goals and directions within the department. Your responsibilities include: being able to maintain an overview, follow up on performances and set directions for everyone in the team ensuring the team/department solves the tasks timely under your guidance to work smarter and more efficiently building and maintaining a close collaboration with the stakeholders and ensure common alignment coordinating and exchanging experiences across teams and departments increasing focus and utilisation of LEAN and new technology such as digitalisation and automation to improve both performance and the working environment across the department Qualifications To succeed in this position, you: preferably have at least 2 years of relevant experience as a people manager have some experience related to quality assurance and/or pharmaceutical production/GMP preferably hold a degree in pharmacy, engineering or equivalent background may have experience working with CMOs possess good communication skills, and you express yourself clearly and distinctly in both Danish and English You are proactively striving for higher levels of performance, not being afraid of being challenged by peers and employees. You are well organized and create strong results by engaging your employees in taking pride in delivering on their objectives. It is natural for you to develop the people around you and you are motivated in creating a high level of commitment for your employees in everyday life. You are determined, decisive and have the will to take the lead both professionally and in collaboration with other professional groups - just as you dare to take the lead and pave the way in both team and department. Your natural sense of the right level of detail helps employees deliver what is needed. You have experience with GMP, quality management and maybe also with audits/inspections. About the department The department is a part of CMC Development QA and located primarily in Måløv and Bagsværd with assignments in other production sites in the greater Copenhagen area as well. We also work with CMO´s worldwide. Currently, we are around 30 highly qualified employees with even more colleagues to join us soon. We are responsible for assuring the quality and compliance of our aseptic filling line in CMC, approve development documents, releasing all parenteral development batches for our clinical trials as well as supporting the business by improving and simplifying processes. Working at Novo Nordisk At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth. Deadline July, 20 Contact For further information, please contact Marianne Mørch Hansen +45 3079 8154 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 Måløv.
Jobbet er oprettet på vores service den 5.7.2023, 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
- Måløv
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Statistik over udbudte øvrige i Måløv over tid
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| 21. september 2024 | 7 |
| 20. september 2024 | 6 |
| 19. september 2024 | 6 |
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| 17. september 2024 | 5 |
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| 12. september 2024 | 12 |
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| 23. august 2024 | 11 |
| 22. august 2024 | 12 |