Associate Manager in Oral Product Development

2 weeks ago


Måløv, Denmark Novo Nordisk AS Full time

Are you a strong people leader motivated by building the right team and making it thrive and perform? Are you ready to make a difference and join an area where the pioneering spirit drives us forward? If yes, we are looking for an Associate Manager with a strong strategic mindset and excellent leadership skills to join us in Oral Product Development (OPDev), a part of the expanding tablet area in Måløv.

The Position

As an Associate Manager, you will lead a team of approximately 15 highly dedicated academics and technicians.

The main tasks will be to:

• Guide, coach, and lead your employees in the team.

• Set the direction for the team and mentor members of your team for individual growth.

• Ensure GMP production activities are compliant and in control, which covers both clinical phase I and II GMP production and development.

• Introduction of new production process concepts coming from early development departments.

• Ensure timely and compliant release of the Phase I and 2 GMP batches.

Your focus must be to drive performance and work with continuous improvements and innovation. You will be a part of an ambitious leadership team who supports and helps each other to reach results for the business.

Qualifications

To succeed in this role, you have:

• A Master’s degree in Pharmacy, Engineering, or similar.

• Several years of experience as a leader and a strong GMP and LEAN mindset.

• Additionally, experience with pharmaceutical processes and preferably tablet production

• Fluency in Danish.

On a personal level, you have a positive can-do attitude. You must have excellent communication skills and a passion for setting structure and standards in an ever-changing complex environment. Furthermore, you must be able to translate strategy into ambitious goals. You can prioritize and make bold decisions. People skills are a must.

About the Department

The department OPDev Pilot Plant consists of 38 highly dedicated employees divided into 3 teams. The department is responsible for the production of tablets for Phase I and II Clinical studies as well as process development productions and tests of our new products, not yet on the market. Furthermore, we are responsible for developing, maturing, and securing the best process to produce our tablets for the benefit of our future patients.

Our department is highly motivated, and this position offers you a unique opportunity to use and strengthen your leadership skills in an exciting environment together with great employees and colleagues. You will experience an enthusiastic working climate where we take personal responsibility for quality, delivery, and each other.



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