Quality Coordinator for Fermentation production facility

at  Novo Nordisk

Quality Coordinator for Fermentation production facility
Category: Quality
Location:Kalundborg, Region Zealand, DK
Do you want to be part of Novo Nordisk and help expand our position as one of the most innovative and successful pharma companies? Would you like to help support production in ensuring right level of Quality and continuous improvements? Do you enjoy analysing data to spot trends, and does inspection and audits excites you?
Then we can offer you an exciting position, where your quality mindset and interest in being close to production while supporting with your in depth GMP/QMS knowledge, will be extremely valuable for us as a company, reaching our ambitious goals and having the right level of quality.

QUALIFICATIONS

To succeed in this position, we expect you to have:

• A minimum of 3 years of experience with GMP from relevant position in the medical industryA Master’s degree within chemistry, life sciences or other relevant field
• Experience with some of the following processes and preferably with most of them: deviation handling, change requests, qualification and validation, environmental monitoring and quality control - in order to be able to provide support on the topics.
• You speak/write professionally English

The position requires a high-quality mindset and the ability to act as a role model in setting the direction in regard to Quality and Compliance issues.
As a person you are curious and able to see opportunities for improvement, and you gain energy by going on shop floor and interacting with the production. You possess the ability to work independently, as well as the ability to collaborate with various groups of employees with different backgrounds.

• Provide support and work as sparring partner on quality matters to ensure compliance with existing and new requirements
• Identify trends and possibilities for improvements across the department, that can reduce complexity and build quality and robustness into the processes
• Prepare the department for internal audits and inspections
• Plan and host training in GMP and QMS
• Prepare trend reports, quality oversight tools, Quality Management Review etc