Drug Product Project Manager

at  Novo Nordisk

Måløv, Region Hovedstaden, Denmark -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate17 Nov, 2024Not Specified06 Nov, 2024N/ANatural Sciences,EnglishNoNo
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Description:

Drug Product Project Manager
Category: Engineering & Technical
Location:Måløv, Capital Region of Denmark, DK
Do you want to drive and impact a variety of early and late-stage drug product development projects? Are you motivated by combining your drug product skills with your passion for project management? And do you want to join a dynamic and highly competent team?
Then this is your call for action. CMC Drug Product and Analytical Development is looking for a new Drug Product Project Manager. Apply today and join us for a life-changing career.

QUALIFICATIONS

To succeed in this role you:

  • Hold a MSc in Pharmacy, Engineering, or another relevant field within natural sciences
  • Have min. 4-6 years of experience and gained in-depth knowledge of working within R&D, drug product development or QA
  • Have a high level of energy to drive activities and engage your colleagues forward
  • Are fluent in written and spoken Danish and English

Apart from that you are result-oriented, take pride in delivering on your milestones, and motivate your colleagues with a positive, forthcoming attitude. You work well independently, although you should also be motivated to cooperate with colleagues and stakeholders across functions and departments.

Responsibilities:

As the Drug Product Project Manager you will be responsible for:

  • The development activities and strategies for drug product formulation and manufacturing, through project management
  • Driving the projects through the different stages of clinical development and collaborate within CMC Development and with our colleagues in Product Supply as well as other areas of the R&D organization or contract manufacturers
  • Leading a sub-project team in an engaging and motivating way and participate in writing and compiling regulatory applications and various internal and external documentation
  • Coordinating the transfer of project activities from our research unit to CMC Development and further on to our manufacturing unit Product Supply or to a contract manufacturer
  • Communicating and coordinating with stakeholders within and outside CMC Developmen

To succeed in this role you:

  • Hold a MSc in Pharmacy, Engineering, or another relevant field within natural sciences
  • Have min. 4-6 years of experience and gained in-depth knowledge of working within R&D, drug product development or QA
  • Have a high level of energy to drive activities and engage your colleagues forward
  • Are fluent in written and spoken Danish and Englis


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

IT Software - Other

Clinical Pharmacy

MSc

Engineering, Relevant Field

Proficient

1

Måløv, Denmark