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.
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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. xjrgpwk
This full-time position includes potential for overseas travel.
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