CVP GMP partner

Are you passionate about quality, compliance and continuous improvements and are you looking for an exciting development opportunity? Then you might be our new CVP GMP partner in the CVP area API Manufacturing 4 (M4).You will get a great opportunity to be part of an exciting area and the opportunity to work alongside experienced colleagues.Your new roleAs GMP Partner you will work across the area API M4 and report to the Senior Manager of API, M4 Business Support. In close collaboration with API, M4 management group, you will be responsible for securing product quality and inspection readiness at all time. Furthermore, with local employees in production you will be responsible for continuously improving the quality culture and systems in API, M4 productions.Your main tasks will be focused on:Always securing full GMP compliance and inspection readinessPlan, prepare, and execute audits and inspections (e.g. PLI)Drive the implementation, integration and coordination of projects coming from NN Global Quality, API or API M4 Management, as CVP implementation leadFollow up on quality problems and drive systematic problem solving to find solutionsDevelop cross functional systems and standards for quality and compliance Continuously contribute to improvement of quality mindset & culture.Joining our department means stepping into a role where you will play a vital part in defining further development of API M4 and API M4 Business Support.Your new departmentYou will be part of API, Manufacturing 4 Business Support, where the job is located. API Manufacturing 4 is part of API. At our sites in Gentofte, Hillerød, and Kalundborg, we are more than 600 colleagues working together to manufacture the API used in life-saving medicine for people living with serious chronic diseases. We work with advanced chemical and biotechnological processes such as cultivation, recovery, purification, and freeze-drying. We bring value to our patients by providing the cleanest possible high-quality API made in accordance with Good Manufacturing Practices (GMP) while constantly optimizing our processes.Your Skills And QualificationsWe're seeking candidates who fulfil the following prerequisites:You have a MSc degree in Chemistry or Pharmacy or another related fieldYou have several years of experience with GMP, compliance, and qualityYou have experience in a manufacturing environment, preferably within GMP and manufacturing processesYou have experience in project management, stakeholder management, and change management You have experience in Science and Risk based Validation (SRV)It is an advantage if you have experience in Six Sigma, but it is not a requirementProfessional proficiency in English and Danish is a must.On a personal level, you have an analytical and curious mindset, a high ability to navigate in complex stakeholder landscape and matrix organization and you negotiate at all levels in the organization. You are motivated by challenging assignments, and you absorb new knowledge quickly, demonstrating great cooperation skills, and your proficiency lies in fostering collaboration and ensuring engagement among other employees while setting the overall Strategic direction.Working at Novo NordiskEvery day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and constant curiosity. For over 100 years, this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.What We OfferThere is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.More information For further information, please contact Lene Bøje Madsen, Director, at +45 30 75 83 42 or lmad@novonordisk.comDeadline14th of November 2025Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.