Global Quality Assurance Manager
2 weeks ago
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.
- 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.
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 OfferIn 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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