IVYWORKS is a Compliance Consulting firm. We provide services to pharmaceutical and biotechnology industries. Visit http://www.ivyworks.net for more info.
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.
Bachelors degree in engineering / science.
2-6 years of work experience is a must.
Experience/exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 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.
Salary: Not Disclosed by Recruiter
Role Category:Drug Regulatory Affairs/Documentation
Role:Drug Regulatory Director
Desired Candidate Profile
UG:B.Tech/B.E. - Any Specialization, Other Graduate, B.Pharma - Pharmacy
Ivy Works Advisors LLP
Contact Company:Ivy Works Advisors LLP