Senior Project Manager

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Senior QA Project Managers for Product Development Projects We are looking for skilled and experienced Project Managers, to play a key role in ensuring quality oversight and deliveries for future products within diabetes and obesity care. In the role you will take the seat as QA in strategic product core groups and be responsible for coordinating input to quality/cGMP metrics for senior management, through collaboration with QA´s across the whole Novo Nordisk value chain. The role offers high impact and influence in ensuring quality throughout the late stages of product development. If this sounds like the job for you, then you might be the person we are looking for in our QA unit for IFP ManDev. The position As Senior QAProject Manager in IFP ManDev (Injectable Finished Products, Manufacturing Development) you will ensure that the quality agenda for our new products is maintained. You will be the central QA in strategic product core groups, representing QA’s across the whole value chain. Your main task is ensuring quality oversight from late product development phases into life cycle management phase. You will plan, coordinate and follow up on QA project activities and deliver ongoing quality status towards senior management. As part of this you will head up groups with “point of entry” area QA’s, from relevant areas across Novo Nordisk, to ensure oversight and deliveries from every corner of QA. Throughstrong coordination, communication and social skills, you will use your talents to set clear quality directions and strategies within product development and implementation stages. The role requires proactive oversight and early collaboration with various stakeholders. You will get great opportunities for both personal and professional development. The role gives you the opportunity to collaborate and network across Novo Nordisk. The area of Manufacturing development offers diverse and complex tasks, and as a team we are involved in various cases with high attention and impact, as well as innovation and digitalisation projects with impact beyond IFP. Qualifications
  • Master’s degree in Biology, Engineering, Pharmacy, Chemistry or similar
  • Proven record of cross functional GMP experience from pharmaceutical industry and strong knowledge within validation
  • Competencies within Project Management
  • You are a self-driven, proactive, and resourceful person
  • Ability to set the right and balanced quality standards and ensure compliance within regulatory requirements
  • You thrive in a dynamic environment where collaboration and communication with many different stakeholders will be crucial for your success
  • Capable of taking tough quality decisions
    • About the department You will become part of a great department with many interfaces around the organisation, both in Denmark and our international production sites. The department consists of around 40 people divided into three teams, with this position being in the Product & Processes team. The team consists of highly knowledgeable and skilled people, covering the diverse area of ManDev and supporting our global production sites. In the department, we take great pride in our work and value challenges as opportunities. We have a vibrant and positive working environment, good values and exchange of knowledge and experience. We all work towards continuously improving our competences, as well as making work processes more efficient and effective. 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 career 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 40,000 employees. Together, we go further. Together, we’re life changing. Contact For further information, please contact Associate Manager Andreas Dupont Rothemejer at +45 3077 6594. Deadline 28th of August 2023. You may submit your application in English or in Danish. We look forward to reading your application, and we will review applications received on an ongoing basis, so do not hesitate 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. 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.


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    Jobbet er oprettet på vores service den 14.6.2023, men kan have været deaktiveret og genaktiveret igen.

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