A large and well-established medical manufacturer with global offices is looking to introduce a Director of Quality and Regulatory Affairs to their site in Belgium.
This role is advertised as on site but a hybrid working structure is up for negotiation.
Responsibilities:
Lead and expand a large quality team, ensuring the quality department is up to regulatory standards and has a clear set of instructions in order to hit internal quotas
Implement and revise quality systems in line with quality regulations such as CAPA and GMP
Facilitate cross-departmental cooperation to ensure good quality practices company-wide.
Manage and oversee audits both internally and externally with the aim of enhancing time management within the quality assurance process.
Qualifications:
Bachelor's degree (essential), and masters (preferable) within a relevant scientific field
Meaningful experience with quality standards and regulations such as ISO 9001, ISO 13485, IVDR/IVDD and GMP
5+ years within the medical devices field
3+ years of managerial experience
Strong organisation, pragmatism, good communication, interpersonal skills and high standards of work
If you are interested in this role, please apply with a CV attached.
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๐:+44 20 7019 4130
