Senior Quality & Data Privacy Partner

at  Novo Nordisk

Senior Quality & Data Privacy Partner
Category: Quality
Location:Søborg, Capital Region of Denmark, DK
Would you like to support the innovation of quality assurance and compliance procedures through process improvement and digitalization within the pharmaceutical industry? Would you like to aid the shaping of a quality and compliance-driven culture, setting the standard for responsible and compliant handling of research data and operational efficiency in a truly global organization?
If yes, then you might be the Senior Quality & Data Privacy Partner to join our newly established Research and Development (R&D) Data Governance Office, aiming to streamline and digitize data retention and deletion efforts within the R&D organization in Novo Nordisk.
Apply now for a life-changing career!

QUALIFICATIONS

To thrive in the role of a Senior Quality & Data Privacy Partner, we seek an individual with the following qualifications:

• Master’s degree in a relevant field (e.g. science, business, commercial law or similar)
• A minimum of 3+ years relevant experience from a similar position working with quality and compliance from a pharmaceutical / life science company
• Strong stakeholder management skills across all levels of seniority combined with excellent communication skills and analytical capabilities (fluent in English, both verbally and written)
• Tech savvy and proficient in MS Office Tools; good understanding of AI-related tools (e.g., ChatGPT, M365 Copilot) would be an advantage
• Experience with compliance in a pharmaceutical context e.g., GxP and GDPR, as well as experience within M&A is considered as a significant advantage

Personally, you are adept at working independently and adapting quickly to new situations in a continuously changing environment. Your robust collaborative skills allow you to effectively participate within teams and across different departments, ultimately improving the overall work environment. Above all, you are a cooperative team player with a proactive, global mindset.

• Master’s degree in a relevant field (e.g. science, business, commercial law or similar)
• A minimum of 3+ years relevant experience from a similar position working with quality and compliance from a pharmaceutical / life science company
• Strong stakeholder management skills across all levels of seniority combined with excellent communication skills and analytical capabilities (fluent in English, both verbally and written)
• Tech savvy and proficient in MS Office Tools; good understanding of AI-related tools (e.g., ChatGPT, M365 Copilot) would be an advantage
• Experience with compliance in a pharmaceutical context e.g., GxP and GDPR, as well as experience within M&A is considered as a significant advantag