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A logistics company for pharmaceuticals is seeking a Regulatory Affairs professional to implement and maintain their Quality Management System (QMS). Responsibilities include reviewing and approving material batches, conducting audits for compliance, and providing training on Good Manufacturing Practices (GMP). The role is vital for ensuring quality standards during ongoing transformation projects. Interested candidates can apply via the provided email.
Our client is a provides temperature-controlled logistics for the global pharmaceutical and biotech industries. Due to business needs, they are now recruiting a Regulatory Affairs to be part of their Team for ongoing transformation projects. They are located in the West - easily accessible.
Interested candidates who wish to apply for the advertised position, please click APPLY NOW or email an updated copy of your resume/cv. We regret that only shortlisted candidate will be notified.
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