Specialist for Oral Development and Due Diligence

Denne stilling er desværre ikke længere ledig.
Se alle ledige stillinger

Måløv

Do you want to be a true pioneer and contribute to the development of oral solid dosage forms? Are you passionate about drug product development and have a strong background in due diligence investigations? If so, read more below and apply now to become part of our team as a Specialist!

About the department In Oral Product Development, we develop drug products ensuring that we bring best-in-class treatments to the market. The department consists of 50+ dedicated and enthusiastic colleagues organised in 3 teams. We are responsible for developing and providing documentation for oral drug products for pre-clinical studies and clinical trials from phase I to phase III. Development of drug product formulations and processes for oral delivery is performed internally and externally. A broad and exciting range of process technologies for development of oral solid dosage forms are available in-house. The department is also responsible for performing due diligences in collaboration with cross-organizational teams.
The position We are seeking a highly motivated and detail-oriented Due Diligence and Product development Specialist to join our Drug Product Development team. In this role, you will be responsible for conducting due diligence investigations on potential drug product development opportunities, providing critical insights to support business decisions. Your main tasks will include:
• Conducting thorough research and analysis on potential drug product development opportunities, including scientific, regulatory, financial, and commercial aspects
• Identifying gaps in available information and working with internal and external stakeholders to fill them
• Collaborating with cross-functional teams to ensure due diligence is conducted effectively and efficiently
• Preparing clear and concise reports summarizing findings and recommendations
• Maintaining up-to-date knowledge of industry trends and regulations and applying that knowledge to inform due diligence investigations Finally, you will contribute to developing formulations and manufacturing processes for new oral drug products, by preparing, executing, and evaluating development studies to ensure the transition of new oral projects from research to clinical trials.
Qualifications
We are looking for someone with strong analytical and problem-solving skills, with the ability to identify and evaluate risks and opportunities. To succeed in this role, you:
• Have a master’s degree within Life Sciences or a related field
• Have at least 5 years’ experience in due diligence within product development
• Ideally have experience within pharmaceutical companies
• Ideally have knowledge of drug product development processes, including scientific, regulatory, and commercial aspects
• Are fully proficient in English

As a person, it comes naturally to you to take initiative and to have a strong personal drive. You thrive in a changing and dynamic environment, working independently and managing multiple projects simultaneously. You can maintain attention to detail, and you are structured when it comes to problem-solving. Furthermore, you have good stakeholder management skills with the ability to build relations and good communication skills, with the ability to collaborate effectively with cross-functional teams.
Working at Novo Nordisk
Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our careers is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 55,000 employees. Together, we go further. Together, we’re life-changing and do it all for our patients.

Contact
For further information please Scientific Director Helle Eliasen at
+45 3075 5574 or Associate Manager Lone Løgstrup Kimer at +45 3079 3569.
Deadline
11 June 2023

We will review applications and conduct interviews on an ongoing basis, so we encourage you to apply sooner rather than later. 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 18.5.2023, 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

Lignende jobs

  • Øvrige i København Ø

    Fri kontakt
    Senior Associates og Managere til Transaction Advisory Service i København. Vi mærker en stigende efterspørgsel efter rådgivning i forbindelse med køb og salg af virksomheder, herunder finansiel due diligence. Derfor søger vi Senior Associates og Managere til vores TAS team på Østerbro.
    • Øvrige
    • København Ø
    Få mere info
  • Øvrige i København Ø

    Fri kontakt
    Vi har travlt, og vi søger nu nye kolleger til vores Transfer Pricing-afdeling.
    • Øvrige
    • København Ø
    Få mere info
  • Øvrige i København K

    Fri kontakt
    Associate til IT Risk Assurance. Vi vækster i Grant Thorntons IT Risk Assurance & Advisory Services, og søger derfor en nyuddannet kollega. I afdelingen beskæftiger vi os med IT-revision, afgivelse af IT-erklæringer (ISAE 3402, ISAE 3000 mv.
    • Øvrige
    • København K
    Få mere info
  • Øvrige i København

    Fri kontakt
    Ansøg senest: 5. maj 2024 København On-site. Smiler du med øjnene, griber bolde fra alverdens retninger og elsker at hjælpe? Så tror vi på, at du er vores Bellboy på Scandic Spectrum. Vi ved, at du er skarp og handler hurtigt, når situationen kræver det.
    • Øvrige
    • København
    Få mere info

Statistik over udbudte jobs som øvrige i Måløv

Herunder ser du udviklingen i udbudte øvrige i Måløv over tid. Bemærk at jobs der ikke har en bestemt geografi ikke er medtaget i tabellen. I den første kolonne ser du datoen. I den næste kolonne ser du det samlede antal øvrige.

Se flere statistikker her:
Statistik over udbudte øvrige over tid

Dato Alle jobs som øvrige
27. april 2024 34
26. april 2024 32
25. april 2024 34
24. april 2024 37
23. april 2024 34
22. april 2024 37
21. april 2024 37
20. april 2024 37
19. april 2024 36
18. april 2024 32
17. april 2024 31
16. april 2024 29
15. april 2024 31
14. april 2024 31
13. april 2024 33
12. april 2024 29
11. april 2024 26
10. april 2024 28
9. april 2024 27
8. april 2024 29
7. april 2024 40
6. april 2024 41
5. april 2024 39
4. april 2024 38
3. april 2024 36
2. april 2024 44
1. april 2024 50
31. marts 2024 53
30. marts 2024 53
29. marts 2024 51
28. marts 2024 48