Quality Process Manager

at  Novo Nordisk

Quality Process Manager
Category: Manufacturing
Location:Bagsværd, Capital Region of Denmark, DK
Would you like to be a part of shaping the future of manufacturing? Are you motivated by leading Quality Processes to excellence across our global sites and do you have exceptional skills in stakeholder management?
If so, come join us as a Quality Process Manager in Aseptic Manufacturing (AM)!

QUALIFICATIONS

We seek a candidate who excels in a dynamic environment, maintaining high work quality. Our ideal candidate collaborates effectively with diverse stakeholders, possesses practical knowledge of manufacturing quality processes, and demonstrates strong leadership skills. While direct management experience is preferred, success in this role hinges on indirect leadership within the network. A background in project management coupled with leadership skills is advantageous.

To succeed in this role, you have:

• An Academic Degree in engineering, pharmacy or similar field.
• At least 5 years of experience within Aseptic Manufacturing with at least some of the years being within or close to the quality processes related to production.
• Experience with project management within a global stakeholder landscape as well as leadership skills.
• Experience within GxP regulated pharmaceutical manufacturing environment.
• Professional proficiency in English.

Additionally, you have experience with LEAN. Moreover, your professional background includes business strategy and projects implementation within global organization. As a person you are a team player with a great ability to collaborate and have strong leadership skills with a proven track record of guiding and motivating teams. You have a “can-do” attitude and believe that no challenges are too big or too small to handle. You are interested in finding new and improved ways to make our processes more efficient. Furthermore, you are a dedicated professional who is eager to learn and develop new skills.

Your key responsibilities will include:

• Setting direction for the Quality processes within compliance.
• Initiating and driving various initiatives and projects to support the above direction.
• Overall responsible for quality process groups focusing on shared success related to the direction for the quality processes.
• Being close to the Quality processes across Aseptic Manufacturing in Europe, North and South America, and Asia.
• Working in close collaboration with other groups (improvement groups, different network groups, other process groups etc.) as well as various stakeholders along the value stream

To succeed in this role, you have:

• An Academic Degree in engineering, pharmacy or similar field.
• At least 5 years of experience within Aseptic Manufacturing with at least some of the years being within or close to the quality processes related to production.
• Experience with project management within a global stakeholder landscape as well as leadership skills.
• Experience within GxP regulated pharmaceutical manufacturing environment.
• Professional proficiency in English