NonStop Consulting

Regulatory Affairs & Quality Assurance Manager – International Exposure

A Medical Device company in the Maastricht-Heerlen region of the Netherlands has an exciting opening for a Regulatory Affairs & Quality Assurance Manager to join its dynamic team. Be a part of an international team and experience firsthand the benefits of working in a small yet internationally connected company.

The role:
As the Regulatory Affairs & Quality Assurance Manager, you will be responsible for maintaining RA, QA, and QC projects, building a balanced QA/QC team, writing registration dossiers, and strategizing international registrations.

Master/PhD degree in Pharmacy or equivalent;
At least five years of relevant international working experience in the medical device, pharmaceutical preferably in RA & QA;
Excellent team management and project management skills;
Knowledge of interpreting and applying laws/regulations, especially related to medical devices;
Fluency in English (oral and written).

Do you have any disability or condition that could affect you in the application and interview process? Please feel free to share this information as part of your application, including any necessary adjustments you might need, so we can help make the process easier for you. We assure you this information will not have any negative effect on the interview process outcome.

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