Our client is a global leader in clinical and commercial packaging solutions for the pharmaceutical and biotech industry. With state-of-the-art facilities and a strong reputation for quality, innovation, and compliance, the company supports customers throughout the full product lifecycle—from design to delivery. * Define, harmonize, and implement global quality policies, standards and procedures, aligned with cGMP, internal requirements, and client expectations. * Lead audits (client, supplier, agency) and manage regulatory filings as needed. * Stay up to date with regulatory trends and represent the company toward health authorities, clients, and suppliers.
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