IVY Works has an opening for full time employee as a Computerized System Validation Specialist or Engineer
Responsibilities
- Developing validation documentation for pharmaceutical equipment, facilities and computerized systems used in GLP, GMP and GCP environments.
- Project Deliverables will encompass validation plans, specifications, test protocols and standard operation procedures and systems may include Process Automation, Laboratory Automation, Enterprise IT Applications and Network Infrastructure.
Experience
- Bachelor's degree in engineering / science.
- 4-6 years of work experience is a must.
- 3+ years of experience/exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5.
- Valuable communication and technical writing skills are a must.
- Project Management experience
Job Location
Our Office is located in Bangalore and the job may involve travel to client locations.
📌 Senior Validation Specialist or Engineer (India)
🏢 Ivy works
📍 India
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