CQV Engineer
Job in
20029, Turbigo, Lombardia, Italy
Listed on 2026-07-02
Listing for:
Altro
Full Time
position Listed on 2026-07-02
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer, Quality Engineering
Job Description & How to Apply Below
Location: Turbigo
Position Summary
We are now seeking a CQV Engineer to join our growing operations in Italy. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and development of summary reports at the client site.
Key Responsibilities
Support documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment.
Write and execute protocols (field verification) and develop summary reports at client sites.
Manage the C&Q documentation and execution lifecycle from SLIA generation through to OQ completion.
Support onsite and offsite activities, including FATs, SATs, IOQ and PQ executions and system walkdowns.
Provide cGMP leadership and guidance for the integration and delivery of CQV services for our Life Sciences clients.
Qualifications
BS or MS in a relevant science or engineering field, or equivalent years of hands‑on experience.
Minimum 4 – 8 years’ experience performing commissioning and/or qualification activities in an FDA‑regulated industry.
Experience in facilities and equipment startup, walk‑downs & troubleshooting, utilities (WFI, RO, HVAC), building automation or other pharmaceutical manufacturing processes and equipment, FAT/SAT, URS, design review, P&IDs, IQ/OQ/PQs, generation & execution.
Excellent technical problem‑solving and troubleshooting skills, solid knowledge of typical project technical issues.
Strong attention to detail, ability to multi‑task, and take initiative to accomplish tasks accurately.
Ability to work independently and quickly build and nurture a project team.
Proficiency in Microsoft Word and Excel.
Excellent oral and written English.
Available for travel in Italy and abroad.
Additional Requirements
Proficient in life science manufacturing processes, e.g., biotech, aseptic processing, aseptic fill/finish, OSD, Gene Therapy (or equivalent experience).
Familiarity with Baseline Guide 5 (Second Edition) is a plus.
Experience with isolator qualification protocols execution and reporting, VHP cycle development, GMP‑based knowledge.
Compensation
The compensation package offered ranges from €34,000 to €45,000 gross per annum. The final salary within this range will be determined according to the candidate’s technical competencies and relevant professional experience.
EEO Statement
La selezione rispetta il principio delle pari opportunità (l. 903/77).
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