Senior Drug Product Project Manager
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Are you passionate about setting strategic direction and driving late-stage drug product development projects? Would you like to collaboration with experiences scientists and interact with stakeholders across the organization? If so, there is a unique job opportunity waiting for you, read more and apply today!
About the department
Oral Product Development (OPDEV) is part of Emerging Technologies (ET), a newly established area in Novo Nordisk. We have a growing pipeline of new products, many of which are based on emerging technology platforms coming into Product Supply via internal development projects and externally acquired assets.
In our department, we manage all oral drug development projects from clinical phase I to one year after launch and ensure robust business processes in the area. You'll be joining a diverse team of Drug Product Project Managers who all work together to make a positive impact on patients' lives.
We are well-known for having a pioneering spirit as well as a curious and daring approach. We play a key role in developing and producing future treatments for millions of patients around the world. By joining our team, you'll have the opportunity to make a real difference in people's lives and work alongside a diverse and supportive team of colleagues.
The position
As Drug Product Project Manager, you will be responsible for:
• Ensure development and manufacturing of drug products in clinical development phases
• Define a clear development strategy together with specialists and key stakeholders using your project management skills
• Drive the project through the different development stages and collaborate with Chemistry, Manufacturing and Control (CMC) project cores members as well as other areas of the R&D organization
• Lead sub-project teams in an engaging and motivating way and participate in writing and compiling regulatory applications and various internal and external documentation
• Communicate and coordinate with stakeholders within and outside ET
In addition, you will be a member of the CMC Project Core Team, where you will be responsible for planning and coordinating development activities within your expertise area and ensure deliverables according to the project plan.
Qualifications
To succeed in this role, you:
• Have a masters’ degree in pharmacy, engineering, chemistry or similar natural science subjects
• Have several years’ experience and gained in-depth knowledge of working within R&D, drug product development or QA in a pharmaceutical setting
• Have extensive project management experience, and qualifications
• Are fluent in English, both written and spoken
It is an advantage if you also have experience with external partnership and/or small molecule-based drug products..
As a person, you have a high-quality mindset and take pride in delivering on your deadlines. You work well independently, although you should also be motivated to cooperate with colleagues and stakeholder across the functions and departments. With your structured approach to your tasks, you maintain an overview - even in a changing environment where priorities can change quickly. Personal drive, energy and a positive attitude are essential.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact Director Lise Agersted at +45 30798459.
Deadline
12 November 2023
Applications for this position will be reviewed on an ongoing basis, so we encourage you to apply as soon as possible.
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.
About the department
Oral Product Development (OPDEV) is part of Emerging Technologies (ET), a newly established area in Novo Nordisk. We have a growing pipeline of new products, many of which are based on emerging technology platforms coming into Product Supply via internal development projects and externally acquired assets.
In our department, we manage all oral drug development projects from clinical phase I to one year after launch and ensure robust business processes in the area. You'll be joining a diverse team of Drug Product Project Managers who all work together to make a positive impact on patients' lives.
We are well-known for having a pioneering spirit as well as a curious and daring approach. We play a key role in developing and producing future treatments for millions of patients around the world. By joining our team, you'll have the opportunity to make a real difference in people's lives and work alongside a diverse and supportive team of colleagues.
The position
As Drug Product Project Manager, you will be responsible for:
• Ensure development and manufacturing of drug products in clinical development phases
• Define a clear development strategy together with specialists and key stakeholders using your project management skills
• Drive the project through the different development stages and collaborate with Chemistry, Manufacturing and Control (CMC) project cores members as well as other areas of the R&D organization
• Lead sub-project teams in an engaging and motivating way and participate in writing and compiling regulatory applications and various internal and external documentation
• Communicate and coordinate with stakeholders within and outside ET
In addition, you will be a member of the CMC Project Core Team, where you will be responsible for planning and coordinating development activities within your expertise area and ensure deliverables according to the project plan.
Qualifications
To succeed in this role, you:
• Have a masters’ degree in pharmacy, engineering, chemistry or similar natural science subjects
• Have several years’ experience and gained in-depth knowledge of working within R&D, drug product development or QA in a pharmaceutical setting
• Have extensive project management experience, and qualifications
• Are fluent in English, both written and spoken
It is an advantage if you also have experience with external partnership and/or small molecule-based drug products..
As a person, you have a high-quality mindset and take pride in delivering on your deadlines. You work well independently, although you should also be motivated to cooperate with colleagues and stakeholder across the functions and departments. With your structured approach to your tasks, you maintain an overview - even in a changing environment where priorities can change quickly. Personal drive, energy and a positive attitude are essential.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact Director Lise Agersted at +45 30798459.
Deadline
12 November 2023
Applications for this position will be reviewed on an ongoing basis, so we encourage you to apply as soon as possible.
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 "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 17.10.2023, 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.
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