Global Quality Assurance Manager

2 weeks ago


Hillerød, Hillerød Kommune, Denmark Novo Nordisk AS Full time
Job Overview

We are seeking an experienced Senior GMP Expert to join our Device Manufacturing Development (DMD) team at Novo Nordisk A/S. As a key member of our Product Control and Global Support department, you will be responsible for managing quality-related activities and driving quality improvement initiatives.

Key Responsibilities
  • Lead and coordinate root cause investigations for potential quality and compliance issues.
  • Drive and implement quality improvements within the department.
  • Ensure a high level of GMP overview, reporting quality trends to management, and supporting daily QC operations.
Requirements
  • Masters degree in pharmacy, biochemistry, production engineering, or similar with practical experience in the pharmaceutical industry.
  • Strong understanding of GMP regulations and requirements.
  • Practical experience with investigations, inspections, and deviations, along with a solid LEAN mindset and experience in using LEAN tools.
  • Excellent stakeholder management skills, setting direction and guiding/coaching.
  • Professional proficiency in English, both spoken and written.
About the Role

This is an excellent opportunity for a motivated and results-driven professional to join our dynamic team and contribute to ensuring the highest quality standards in our products.

You will work closely with cross-functional teams, providing guidance and coaching to colleagues and contributing to the development of quality-focused processes.

What We Offer

In this role, you will have the opportunity to work on challenging projects, develop your skills and expertise, and grow professionally in a supportive and inclusive environment.

We offer a competitive salary package, including a base salary of approximately 120,000 DKK per year, depending on experience, as well as opportunities for career growth and professional development.



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