Pharma Validation Engineer – Commissioning & Qualification

Commissioning Agents Inc; Milano; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading engineering firm in Italy is seeking a Validation Engineer to support documentation for commissioning and validation of pharmaceutical facilities. The role involves developing protocols, managing the C&Q documentation lifecycle, and providing cGMP guidance. Applicants should have a BS or MS in relevant fields and 3-5 years of experience, along with strong problem-solving skills and proficiency in Microsoft Office. Availability for travel throughout Italy is required.

Competenze

• 3–5 years of experience in commissioning and/or qualification activities in FDA-regulated industry.
• Strong understanding of life science manufacturing processes.
• Excellent oral and written English skills.

Mansioni

• Develop protocols for validation, execution, and reporting at client sites.
• Support documentation for commissioning, qualification, and validation.
• Manage the C&Q documentation lifecycle from SLIA to OQ completion.

Conoscenze

cGMP knowledge

Technical problem-solving

Microsoft Word proficiency

Microsoft Excel proficiency

Team building

Formazione

BS or MS in a relevant science or engineering field

Strumenti

FAT/SAT

WFI

RO

HVAC

P&ID

Descrizione del lavoro

A leading engineering firm in Italy is seeking a Validation Engineer to support documentation for commissioning and validation of pharmaceutical facilities. The role involves developing protocols, managing the C&Q documentation lifecycle, and providing cGMP guidance. Applicants should have a BS or MS in relevant fields and 3-5 years of experience, along with strong problem-solving skills and proficiency in Microsoft Office. Availability for travel throughout Italy is required.