Manager with Analytical and/or RA experience

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Gentofte

Do you want to collaborate on setting direction in a dynamic department with a diverse range of tasks within the implementation of new products, life cycle management of marketed products, and development of automation and new technologies? Are you eager to lead and develop a team of regulatory writers and reference material coordinators? If so, we have a great opportunity in our fantastic department Biotech and Rare Disease (BRD) Analytical Manufacturing Development. Join us, apply today! The position You will lead the Analytical Product Support team of 12 highly skilled professionals. The team is responsible for writing regulatory documents throughout the product lifetime as well as ensuring that we always have reference materials available at the right time and quality. Your focus area is to set direction for the team together with developing and supporting the employees. Besides collaboration in the management team, you will be in close dialogue with a variety of departments across Novo Nordisk, among others BRD Quality Control (QC) and Regulatory Affairs. Qualifications To succeed in this position, you: • Hold a Master’s degree in Science within Pharmacy, Chemistry, or a similar field • Have a minimum of 2 years of managerial experience and thrive in the leadership role • Preferably, you have worked within Regulatory Affairs for a shorter or longer period • Are fluent in English, and preferably in Danish Moreover, as a leader, you earn trust and respect from colleagues and employees and know how to motivate others. You have a can-do approach and get energized by delivering results for our business. While enabling others to succeed, you enjoy succeeding yourself. About the Department Our department is part of BRD Manufacturing Development, also known as MSAT (Manufacturing, Science and Technology). We are situated in Gentofte close to Copenhagen. There are five teams in the department. In total we are around 65 colleagues who are responsible for supporting QC with new analytical technology and automation. We validate analytical methods during transfer from Chemistry Manufacturing Control (CMC) to QC; we manage the analytical part of BRD projects when new products are handed over from CMC, and throughout life cycle management; we ensure excellent internal and external analytical documentation of our products; and we ensure presence and documentation of reference materials for all BRD products. A department with complex challenges, a great work environment, and good collaboration across the department. Working at BRD, Novo Nordisk BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD, we are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology. Working at Novo Nordisk At Novo Nordisk your skills, dedication and ambition help us change lives for the better. In exchange we offer you to work with extraordinary talent and give you the opportunity to get an insight into a complex business area where culture, politics, a broad product range and various manufacturing sites are part of the daily business. Contact For further information, please call Director Ann J.L. Mürer at mobile +45 3075 7796. Deadline 26th of October 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 Gentofte.

Jobbet er oprettet på vores service den 16.10.2023, men kan have været deaktiveret og genaktiveret igen.

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  • Øvrige
  • Gentofte
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