•Main Objective: As Quality Assurance Professional you will be part of an international network of fellow professionals and you will always be able to draw on the collected knowledge and experience of dedicated colleagues.
-Ensure products and business processes meet GMP, Novo Nordisk and local requirements.
-Ensure products and processes meet GMP, Novo Nordisk and local quality standards.
-Follow-up of internal & external audits and self-inspections
-Ensure document control process
-Ensure archiving process retention program
-Ensure and follow-up the training program
-Ensure back up functions
-Academic degree in Biology, Chemistry, Pharmacy or similar field
-At least 3 years of relevant experience working with establishment of Device/Pharmaceutical manufacturing and/or manufacturing Pharmaceutical products
-The ideal candidate will need an open mindset who can work independently and as a team player with a strong focus on results, to succeed in this role
-Good communication skills with the ability to establish good relationship with local and global team
-Fluent in English, both written and oral
-Ideal Age Range: 25 - 50
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Novo Nordisk Pars
Novo Nordisk is a world leader healthcare company in diabetes care, having the broadest diabetes product portfolio in the industry, including the most advanced products within the area of insulin delivery systems. In addition, Novo Nordisk has a leading position within areas such as haemostasis management, growth hormone therapy and hormone replacement therapy. Novo Nordisk manufactures and markets pharmaceutical products and services that make a significant difference to patients, the medical profession and society.
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