Generation/update and control of Quality Manual, Quality Policy and procedures/instructions, technical documentation based on the regulatory requirements. Day-to-day follow-up to ensure that the finished product is correctly processed, checked, released and stored according to the defined specifications and procedures.Handling of internal and external audits, changes, risks and deviations.Handling of validation work (e.g. equipment qualification, clean rooms and processes/products). Handling of complaints and product recall.Evaluation of suppliers.Handling of clinical evaluation and post market surveillance.Handling of CAPA plans.

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