QA Manager for Manufacturing Development

The position

As a Manager in IFP (Injected Finished Products) QA for Manufacturing Development, you will be responsible for a team of skilled and experienced QA professionals and specialists and report directly to the director. Your key responsibilities will include:• Motivating, leading, empower and setting directions for your team members• Supporting your team members in complex cases• Ensuring skills and competencies in the team are in place• Building and maintaining strong collaborations with our stakeholders• Keeping the processes simple and continuously striving for improvements You will be growing personally and professionally by developing your leadership competencies and responding to exciting challenges with a high impact on the results for both the CVP area as well as the entire IFP. Our working environment is flexible, dynamic, and informal with a strong culture of cross-functional collaboration. Qualifications To succeed in this position, you:• Hold a master’s degree in pharmacy or biotechnology or other nature science based relevant fields• Have acquired experience from a pharmaceutical industry and project or people management positions• Preferable have experience within production processes and/or QC/laboratory• Have a strong quality mindset, well-developed business sense and problem-solving skills• Communicate fluently in English, and preferably Danish We are looking for a visible leader who can see the big picture and proactively strives for higher levels of performance. Furthermore, you are structured and well organized and create strong results by engaging your employees in taking pride in delivering on their objectives and individual development. About the department IFP Manufacturing Development is a support function to IFP, supporting all processes and products within it. IFP QA Manufacturing Development is the quality department which ensures that quality is incorporated in all aspects. Our department consists of 48 highly qualified employees divided into teams of QC, Products & Processes, and Support. We are responsible for assuring quality and compliance of QC laboratories and Manufacturing Development activities for IFP production sites across the world as well as performing project management for cross-organizational projects, driving digitalization in IFP QA, and supporting with audits and inspections. You will be a part of a department that works in a vibrant and positive working environment and values the exchange of knowledge and experience. Networking, high level of knowledge and cooperation are key to our success. 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 careers 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 50. employees. Together, we go further. Together, we’re life-changing.