Senior Project Manager for manufacturing development department
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- Manufacturing
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Do you want to work with a portfolio of Drug Substance improvement projects to continually support and strengthen Novo Nordisk as a world leading insulin and GLP1 manufacturer? If so, DAPI MDEV, Project Office offers you the opportunity to be part of a team where high engagement, innovation and ambition are key words in solving the everyday challenges.
About the department
DAPI Project Office is a department in Diabetes Active Pharmaceutical Ingredient Manufacturing Development. We execute quality improving, capacity expanding and cost saving projects. Supporting a project structure that secures continuous optimization across DAPI. We manage Development Projects in the phase from CMC-development to DAPI production (process challenge, establishing production facilities, production of API for clinical trials in DAPI, intermediate and API stability, TDR, TTD, validation of production facilities, transfer of analytical methods from CMC to DAPI, RA-documents).
In the team – and the department as a whole – we are proud about our balance between ambitious goals, working hard and maintaining a healthy and fun approach to our tasks. You will be joining an effective, skilful and inclusive team, where you will never be alone with the hard challenges or in celebrating your victories.
The Job
As Senior Project Manager you drive a portfolio of cross organisational projects with high impact on DAPI. You will be responsible of lifecycle management projects for Degludec and Detemir Substance and heading up the project groups with members from e.g. QA, RA, QC, Production and Manufacturing Development. Your main role will be to inspire and motivate the project group to deliver excellent results by ensuring clear project scopes, integrated use of risk management and project plans that secures transparency for all key stakeholders. Further, it is your responsibility to identify and capture improvement ideas securing an overload of opportunities making it possible to assess and prioritize the best project ideas to ensure a continuously improvement of the processes.
You will be responsible for project related communication to stakeholders (e.g. DAPIman, DFP, Sourcing, QA and RA) and act as the main entry for process/product related questions, including coordinate answers to questions from authorities and address patent questions/possibilities.
Qualifications
You hold a MSc in pharmacy, biology, engineering or similar, supplemented with a minimum of 5 years’ experience as a project manager within medical production. You are confident working in a GMP regulated environment. You have profound insight into systematic problem solving. On a personal level, you are a self-starter who thrives with driving tasks independently. As you have a structured approach to your work, you can juggle several processes while prioritising your efforts optimally. You have a global mind-set and enjoy building relations across organisational levels, work cultures and geography. Impeccable communication skills are a must as well as the ability to prepare presentation material in a high quality. Lastly, you must be confident in both written and spoken English.
Feel free to submit your application & CV in English or Danish.
Contact
For further information, please call Ulla Falkenberg on +45 3075 8890.
Deadline
8. January 2020
Information og data
Denne ledige stilling har jobtypen "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 17.12.2019, 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.
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