Overview
Are you a CSV expert passionate about automation, compliance, and helping deliver life-saving medicines? Our client, a leading aseptic drug product facility, is expanding their automation project support team.
Responsibilities
* Act as the Subject Matter Expert for Computer System Validation (CSV), supporting automation projects across formulation, filling, lyophilisation, and packaging.
* Prepare and execute validation documentation, perform risk assessments, review vendor protocols, and ensure compliance with GxP, 21 CFR Part 11, and GAMP 5.
What You’ll Need
* Degree in Engineering, Computer Science, or related field
* 5+ years of control systems validation experience in pharma/biotech
* Expertise with PLC/SCADA systems & OSIsoft PI validation
* Strong understanding of GAMP SDLC & regulatory requirements
Why Join
* Competitive contract rates
* Long-term opportunity with a leading global manufacturer
* Be part of a team committed to continuous improvement & innovation
Application
Apply now or reach out directly: William@eu-recruit.com
Job details
* Seniority level: Mid-Senior level
* Employment type: Full-time
* Job function: Engineering and Manufacturing
* Industries: Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Biotechnology Research
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