Quality Assurance Professional for Global Pharmaceutical Operations
2 weeks ago
We are seeking a highly skilled Quality Assurance professional to join our team in overseeing quality control processes for outsourced drug substance production activities worldwide.
Key Responsibilities- Conduct QA reviews of analytical documentation from Contract Manufacturer Organizations (CMOs) including protocols and reports for method validation.
- Communicate effectively with CMOs via teleconferences to ensure compliance and quality standards.
- Maintain up-to-date knowledge of relevant guidelines and regulatory requirements to ensure adherence to industry standards.
This role requires sporadic travel days per year due to international manufacturer locations.
Qualifications and Requirements- An academic degree in a relevant field such as pharmacy, chemistry, engineering, or similar is required.
- A minimum of 5 years of experience within the pharmaceutical industry or a similar field is necessary.
- Solid understanding of quality and GMP requirements is essential.
- Fluency in English and good Danish language skills are required.
GCM QA DS is responsible for quality assurance and support to outsourced drug substance production activities worldwide. Our department consists of 48 professionals divided into areas focusing on operations, projects, or QA for QC & System Support.
You will join a team of dedicated colleagues who come together to set direction and support GCM QA through its rapid journey of growth. We are office-based and collaboration with diverse stakeholders internally and externally is essential for our success.
Working at Novo NordiskWe drive change and strive for excellence without fixating on perfection. We never shy away from opportunities to develop and seize them. From research and development to manufacturing, marketing, and sales - we're all working to improve patient care.
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