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Senior Quality Specialist for Diagnostics Development
1 week ago
We are seeking a Senior Quality Specialist to join our team in Novo Nordisk A/S's R&D Quality Operations department. The ideal candidate will have a strong background in quality assurance, regulatory affairs, or clinical research, with a focus on In-Vitro Diagnostics.
In this role, you will be responsible for providing quality assurance support to our research and development teams, ensuring compliance with IVD regulations and other relevant requirements. You will also collaborate with cross-functional teams to drive the development of our IVD solutions.
Your Key Responsibilities:
- Ensure compliance with IVD regulations and other relevant requirements.
- Support the development of our IVD solutions through quality assurance and risk management.
- Collaborate with cross-functional teams to drive project execution and delivery.
- Develop and maintain quality management systems to ensure efficient and effective quality processes.
- Participate in audits, inspections, and supplier qualifications to ensure compliance with regulatory requirements.
What We Offer
At Novo Nordisk A/S, we offer a dynamic and challenging work environment that fosters innovation and growth. Our employees enjoy a range of benefits, including competitive salaries, comprehensive health insurance, and opportunities for professional development.
We value diversity and inclusion in the workplace and strive to create an environment where everyone feels welcome and empowered to contribute. If you are passionate about quality and regulatory affairs, and want to be part of a leading global healthcare company, we encourage you to apply for this exciting opportunity.