What are the responsibilities and job description for the Computer Systems Validation Engineer position at Pharmaceutical Company?
We are seeking an experienced IT/OT Computer Systems Validation (CSV) Engineer to support regulated manufacturing systems within a GMP pharmaceutical environment. This role partners closely with system owners to manage the full lifecycle of Level 2–3 ISA-95 systems, ensuring compliance, validation, and ongoing operational readiness.
The ideal candidate brings strong CSV/CSA expertise, hands-on experience with manufacturing and automation systems, and a solid understanding of FDA and global regulatory requirements.
Key Responsibilities
- Support validation, maintenance, and lifecycle activities for IT/OT manufacturing systems (Level 2–3).
- Create, execute, and maintain CSV documentation (protocols, reports, periodic reviews).
- Own QMS records including deviations, CAPAs, and planned events.
- Collaborate with system owners and global stakeholders to ensure GMP and data integrity compliance.
Salary : $62 - $84