Associate Manager for Market Release QC

at  Novo Nordisk

Måløv, Region Hovedstaden, Denmark -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate24 Nov, 2024Not Specified19 Nov, 2024N/AGmp,Deliverables,Leadership,Communication Skills,Biochemistry,Independence,Pharmaceutical Industry,English,Chemical Engineering,Interpersonal SkillsNoNo
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Description:

Associate Manager for Market Release QC
Category: Quality
Location:Måløv, Capital Region of Denmark, DK
Are you an authentic people leader with a track record of leading a team to success? Do you have natural talent for both changing and running the business? If so, this might be the right opportunity for you!

QUALIFICATIONS

To be successful in this role, you have:

  • A Bachelor’s, Master’s, or equivalent degree in Pharmacy, Biochemistry, Chemical Engineering or related field.
  • Proven experience as a people leader, who builds trust, drives engagement and ensures wellbeing in the team.
  • Experience with and understanding of GMP.
  • Preferably experience from QC, but as a minimum you have an understanding for the analytical field preferably from the pharmaceutical industry.
  • Fluency in Danish and English.

As a person, you have solid stakeholder management and communication skills, and you are authentic with strong interpersonal skills that enables you to build trust. We expect you to be a people leader by nature with the ability to coach and lead others in a busy environment. You are robust and renowned for your strong interpersonal skills and ability to set challenging goals and challenge status quo. By working in a structured manner with a non-compromised focus on quality and deliverables, you have a can-do mind-set and focus on opportunities rather than limitations and provide the right balance between leadership and management to your team.
Lastly, you have a high degree of independence and take initiative to challenge ways of doing things and to drive innovative improvements.

Responsibilities:

Your key responsibilities will be to:

  • Ensure efficient daily operations in compliance with GMP and corporate standards, whilst optimising our internal flow.
  • Make sure high performance is met and that the team meets project, quality, and organisational goals.
  • Lead and participate actively in board meetings, process confirmation and structured use of problem-solving tools to locate and eliminate the root cause of an error.
  • Foster a climate of high well-being and innovation within own team and across related organisational departments.
  • Motivate your team towards what is best for both the business and the team, together with your team ensure prioritisation and willingness to adapt to changes and new priorities

To be successful in this role, you have:

  • A Bachelor’s, Master’s, or equivalent degree in Pharmacy, Biochemistry, Chemical Engineering or related field.
  • Proven experience as a people leader, who builds trust, drives engagement and ensures wellbeing in the team.
  • Experience with and understanding of GMP.
  • Preferably experience from QC, but as a minimum you have an understanding for the analytical field preferably from the pharmaceutical industry.
  • Fluency in Danish and English


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Information Technology/IT

Pharma / Biotech / Healthcare / Medical / R&D

Software Engineering

Graduate

Chemical, Engineering

Proficient

1

Måløv, Denmark