Senior Process Manager for Stability of Drug and Combination Product Process
Novo Nordisk
Would you like to be a part of shaping the future of manufacturing? Are you motivated by leading the Stability of Drug and Combination Product Process to excellence across our global sites and do you have exceptional skills in stakeholder management?If so, come join us as a Senior Process Manager for the Stability Drug and Combination Product Process in our business unit Aseptic Manufacturing (AM)!The position
As a Senior Process Manager for the Stability Drug and Combination Product Process, you will be the lead of the process across our global manufacturing sites in the Aseptic Manufacturing (AM) unit and leading the process across Novo Nordisk. You will collaborate with stakeholders both locally and globally and work closely with Senior Process Manager for other processes. You will set direction for the Stability process across all our global sites and ensure that the process is in compliance, standardized and simplified. In this role, you will strengthen and scale our Stability process and shape it with process groups across our sites. Additionally, you will manage a few other processes within the Develop Methods area, focusing on AM.Your key responsibilities will include:Being close to the Stability process and local responsibles across AM sites located in Europe, North and South America, and Asia to understand challenges and close the process in other organisations in Novo Nordisk.Working closely with other processes and groups (improvement groups, different network groups, other process groups etc.)Working with various stakeholders along the value stream.In this role you will be tasked with setting direction and delivering results that have a significant impact on our Stability process. You will be responsible for analyzing data to make sure we focus our efforts where the value and impact is most needed and drive/own initiatives to continues improve the process.Travelling to other sites can be expected aside from the virtual collaboration.QualificationsTo succeed in this role, you have:An Academic Degree within pharmacy or similar field combined with at least 7 years of experience within GMP manufacturing with some of the years being within or close to the stability testing process related to Aseptic GxP production.Experience with project management within a global stakeholder landscape as well as experience within GxP regulated pharmaceutical manufacturing environmentLeadership experience is an advantage.Track record in creating followership through changes in how we work.Professional proficiency in English.On a personal level, you excel in fast-paced environments, maintain high work quality, and enjoy cross-cultural collaboration. Strong leadership skills with a proven track record, direct management experience, and the ability to lead stakeholders indirectly are preferred. With a background in business strategy, project management, and implementation within a global organization, you are a team player with a “can-do” attitude. You are eager to learn, innovate, and improve process efficiency.
Bagsværd, Hovedstaden
Wed, 23 Oct 2024 22:06:44 GMT
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