A leading contract manufacturer in Emilia-Romagna seeks a qualified Process Validation Specialist responsible for planning and documenting validation activities to ensure compliance with ISO 13485 and regulatory requirements. The role involves collaboration with Production and Engineering, handling change control, and supporting continuous improvement initiatives. Candidates should have a relevant engineering degree and 2-5 years of experience in process validation, particularly in the medical device sector. This full-time position includes potential for overseas travel.
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