07 set - Italia
Pharmatec
Company Description
Pharmatec Srl, founded in 2007, specializes in providing comprehensive consulting services across the Pharma, Biotech, Chemical, Medical Devices, and Healthcare sectors. The company is driven by a team of skilled and passionate professionals who bring diverse expertise to every project. At Pharmatec, teamwork and open collaboration are at the heart of achieving success, with team members encouraged to share ideas and experiences. We prioritize continuous professional development to ensure our team delivers high-quality, client-focused services.
Role Description
We are currently looking for an experienced CQV Engineer to support a pharmaceutical project in Lombardy, Italy.
Key Responsibilities:
Execution of Commissioning & Qualification activities (IQ/OQ)
Preparation, review and execution of qualification protocols and reports
Review of URS, FAT/SAT and vendor documentation
Support during walkdowns, punch list management and system handover
Management of deviations and change controls
Coordination with Engineering, Quality,
Operations and equipment vendors
Ensure activities are performed in compliance with GMP requirements and project procedures
Requirements:
Solid CQV experience within the pharmaceutical industry
Strong knowledge of GMP and Commissioning & Qualification processes
Hands-on experience with IQ/OQ execution and documentation
Fluent Italian – mandatory
Availability to work on-site in Lombardy
Previous experience on pharmaceutical manufacturing projects is highly desirable
Contract details:
? Lombardy, Italy – On-site
? Initial duration: 8 months, with possible extension
? Freelance / Partita IVA preferred
? Contact: (email hidden)
Pharmatec SRL is an equal opportunity employer. We welcome applications from all qualified individuals, regardless of race, color, religion, gender, sexual orientation, gender identity, nationality, or disability.
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