Drug Product Project Manager
at Novo Nordisk
Måløv, Region Hovedstaden, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 17 Nov, 2024 | Not Specified | 06 Nov, 2024 | N/A | Natural Sciences,English | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
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