QA Senior Project Manager for Product Development
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Do you know how to set clear quality direction and give precise input to the management team and at the same time communicate it the right way and build strong relationships?
We are looking for a person that wants to use knowledge of different pharmaceutical areas to ensure that the quality status to management represents the correct risks from the various areas. As our new cross functional QA Project Senior Manager for Product Development you will get great possibilities to set your own footprint and be THE central QA. To ensure quality oversight across the different areas involved in product development, we are looking for a skilled and experienced Project Manager, to be the central QA in product development projects. For new products within diabetes and obesity care, the role includes taking 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 (Injectable finished products, Manufacturing Development). You will get great opportunities for both personal and professional development. The role gives you the opportunity to collaborate and network across Novo Nordisk, while building upon your personal skills. The position This role is anchored around ensuring quality overview, for our new products. You will be the central QA in strategic product core groups, where you will be representing QA across the whole value chain and set clear quality direction for the core groups. The projects in scope are for injectable diabetes and obesity products, where many different areas, e.g. QC, Raw Materials, API, are involved. This role will ensure centralized quality oversight from late product development phases into life cycle management phase, across the different areas. You will plan, coordinate and follow up on QA project activities and deliver ongoing quality status towards Senior Management. To ensure inputs from all relevant areas, you will have a network of “point of entry” area QA’s, from areas across Novo Nordisk, enabling oversight for every corner of QA.
To succeed in this role, with setting clear quality direction and giving precise input to management, you will use your: Strong communication, coordination and social skills. You will need to build strong relationships and networks to ensure we have the correct quality status at the right time. You will use knowledge of different pharmaceutical areas to ensure that the quality status to management represents the correct risks from the various areas.
Qualifications Master’s degree in Biology, Engineering, Pharmacy, Chemistry or similar Extensive 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 October 23rd 2023. You may submit your application in English or in Danish. 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 are looking for a person that wants to use knowledge of different pharmaceutical areas to ensure that the quality status to management represents the correct risks from the various areas. As our new cross functional QA Project Senior Manager for Product Development you will get great possibilities to set your own footprint and be THE central QA. To ensure quality oversight across the different areas involved in product development, we are looking for a skilled and experienced Project Manager, to be the central QA in product development projects. For new products within diabetes and obesity care, the role includes taking 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 (Injectable finished products, Manufacturing Development). You will get great opportunities for both personal and professional development. The role gives you the opportunity to collaborate and network across Novo Nordisk, while building upon your personal skills. The position This role is anchored around ensuring quality overview, for our new products. You will be the central QA in strategic product core groups, where you will be representing QA across the whole value chain and set clear quality direction for the core groups. The projects in scope are for injectable diabetes and obesity products, where many different areas, e.g. QC, Raw Materials, API, are involved. This role will ensure centralized quality oversight from late product development phases into life cycle management phase, across the different areas. You will plan, coordinate and follow up on QA project activities and deliver ongoing quality status towards Senior Management. To ensure inputs from all relevant areas, you will have a network of “point of entry” area QA’s, from areas across Novo Nordisk, enabling oversight for every corner of QA.
To succeed in this role, with setting clear quality direction and giving precise input to management, you will use your:
For further information, please contact Associate Manager Andreas Dupont Rothemejer at +45 3077 6594. Deadline October 23rd 2023. You may submit your application in English or in Danish. 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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Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 5.10.2023, 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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