- Provide Compliance support for International Operations (IO) and North America Operations (NAO), focusing on Deviations, cold chain validation, and Change Request (CR) handling.
- Collaborate with OQCP/HQ specialists for timely support and follow-up on goals.
- Support setup and continuous improvement of Deviations, validation, and CR handling.
- Provide timely, specific, and quality support for Deviations, Qualification, and CRs.
- Assist in improvement projects, reporting to Management, and relevant tasks.
- University/equivalent degree (Pharmacy, Biology, Chemistry, Engineering or similar).
- Overall, 6-8 years of experience from the pharmaceutical industry
- Adept in handling Deviations
- Trained and worked according to international validation principles
- Experience with Change Request handling
- Experience with GMP/GDP on operational level
- Intercultural experience
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Senior Quality Professional I - Bengaluru, India - Novo Nordisk A/S
Description
Department : Operations Quality Consulting & Projects
Are you an experienced quality professional looking for a new challenge? Do you thrive in a fast-paced and dynamic environment? We are seeking a Senior Quality Professional to join our team at Novo Nordisk. If you are passionate about ensuring compliance and driving quality excellence, then read on and apply today for a life-changing career.
The Position
As a Senior Quality Professional at Novo Nordisk, you will:
Qualifications
To be successful in this role, we are looking for candidates with the following qualifications:
About the department
The Senior Quality Professional position is part of the Operations Quality Consulting and Projects (OQCP) team. Based in Denmark, the OQCP team supports over 80 affiliates across Novo Nordisk with deviations, change controls, and qualification processes. As a member of the OQCP team, you will play a vital role in ensuring compliance and maintaining the Novo Nordisk Quality Management System in affiliates functions.