Lead Quality Systems Specialist
8 hours ago
Novo Nordisk A/S is seeking a skilled professional to drive the quality agenda of our department and ensure compliance with regulatory requirements.
About the DepartmentThe Chemistry, Manufacturing and Control (CMC) Development & Scaling department makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for clinical trials and have a strong culture with a can do mind-set.
Job DescriptionAs our new colleague, your most prestigious job is to drive the quality agenda of the department, as well as monitor and ensure that the department complies with the Novo Nordisk Quality Management System.
- Drive quality-related tasks and projects across the department.
- Be the department's go-to person in relation to cross-functional quality projects where you will be coordinating and implementing changes.
- Set quality goals for the department and ensure that the quality system is compliant with regulatory requirements.
To be successful in this role, we imagine that you:
- Hold a minimum of a bachelor's degree in Engineering, Chemistry, Pharmacy, or another relevant field.
- Have at least 3-5 years of experience from working within a GMP regulated area.
- Have experience with the LEAN way of working/mindset.
- Are fluent in English, both written and spoken.
As a person, you show initiative and are curious. You work systematically to strive for simplicity in processes and are action and goal-oriented. You are self-motivated, can work independently, but also thrive in being part of a team. You have a can-do attitude.
BenefitsWe offer a dynamic and inclusive work environment where you can grow and develop your skills. Our days are dynamic, they vary, and we are flexible as we are both working on scheduled projects and unplanned tasks to ensure that the production can run smoothly.
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