IVY Works has an opening for full time employee as a Validation Specialist or Engineer.
- Working on validation and compliance projects for clients. The projects will include developing validation documentation for pharmaceutical and biotechnology 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 Pharmaceutical and Biotech Manufacturing Equipment, Facilities, Utilities, and Process Automation.
- Bachelor's degree in engineering / science.
- 2-4 years of work experience is a must.
- Experience/exposure to Equipment Validation, Facility Validation and GAMP 5
- Good communication and technical writing skills are a must.
Our Office is located in Bangalore and the job may involve travel to client locations.
