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GMDP-0080

Freelance CQV Engineer / Consultant – Pharma & Life Sciences

Beschikbaar
20
Jaren ervaring
Validation / Qualification
Specialisatie
Duitsland
Locatie
Over deze expert

CQV Engineer with 20+ years in GMP-regulated pharma environments. Expert in DQ/IQ/OQ/PQ, cleanroom qualification (ISO 14644), HVAC, MEP interfaces, FAT/SAT, commissioning, and audit-ready GMP documentation.

Competenties

Expert
Facility qualification IQ/OQ/PQ Validation Equipment qualification
Gevorderd
Change Control Process validation SOP Writing & Review
Gemiddeld
CAPA Management Regulatory inspection support Deviation Management Vaccines Computer system validation

Certificeringen

GMP Training Cleanroom Technology / ISO 14644 GAMP5 Occupational Safety / PPE
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