Description

Job Description 
Preparation & review of quality mgmt system, qualification protocol, reports, validation, SOP's, STP's specification, APQR, site master file, quality manual, VMP. Vendor audit, market complaint handling, compliance to audit, improve regulatory audit.
Salary: Best in the Industry
Industry:Pharma / Biotech / Clinical Research
Functional Area:Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology
Role Category:Drug Regulatory Affairs/Documentation
Role:Documentation/Medical Writing
Keyskills
compliance audits regulations audits quality management system qms APQR SOP STPs market complaints validation qualification protocols CAPA Site Master Quality Manual VMP vendor audits specifications
Desired Candidate Profile
Commitment towards quality, Passion for excellence, Result oriented & Multi tasking. Excellence in communication skills. Problem solving skills, people management, Co-ordination & planning.
Education-
UG: B.Pharma - Pharmacy
PG:MS/M.Sc(Science) - Any Specialization, Chemistry
Doctorate:Doctorate Not Required
Company Profile:
ZIM LABORATORIES LIMITED
Zim Laboratories Limited: we are a WHO GMP & EU GMP certified and ISO 9001:2008 accredited, We are engaged in research and development, manufacturing of pharmaceutical dosage forms such as tablets, capsules, pellets etc.
Recruiter Name:Deepika Lokhande
Contact Company:ZIM LABORATORIES LIMITED
Email Address:hrd@zimlab.in
Website:http://www.zimlab.in
Telephone:+91-7118-271470
Reference Id:ZLL2912201