Compliance QA Professional for IT Solutions
1 month ago
We are seeking a highly skilled Compliance QA Professional to join our team at Novo Nordisk Pharmatech A/S in Køge. As a Compliance QA Professional, you will be responsible for ensuring the quality and compliance of our IT solutions and services in a regulated environment.
Key Responsibilities- Act as a QA partner regarding GMP compliance towards the IT department
- Approval of deviations, change requests, qualification, and validation documentation
Novo Nordisk Pharmatech A/S is a leading global supplier of high-quality ingredients for the biopharmaceutical and pharmaceutical industries. Our QA/RA department currently consists of 20 employees working diligently to support the entire value chain, from Research & Development to Production and finally Sales & Marketing.
Requirements- An Academic degree within Engineering, Science, Pharmacy, Chemistry, Biotechnology, IT/automation or similar
- Experience within Quality Assurance, Quality Control, Production Support or similar
- Experience with GMP (Good Manufacturing Practice)
- Flair for, and interest in, IT; experience with software validation would be an advantage (GAMP5)
- Professional proficiency in English; knowledge of Danish will be considered an advantage
Novo Nordisk A/S is a fully owned subsidiary of Novo Nordisk A/S situated in Køge. We are a leading global supplier of high-quality ingredients for the biopharmaceutical and pharmaceutical industries, supplying products such as recombinant insulin for cell growth media and pharmaceutical grade quaternary ammonium compounds as well as raw materials for Novo Nordisk A/S.
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