Education: UG -B. Tech/B.E. - Computer/B-Pharm/M-Pharm
Work Location: Goa
General Shift.
Immediate Joinee preferred only
Skills: Hands-on with pharma based applications like LIMS, LMS, DMS, SAP, TrackWise and like others. Job Requirements:
A CSV consultant will use his/her knowledge of FDA cGMP and related regulations and guidelines, and specific knowledge of computer validation methodologies and principles to perform CSV on a variety of systems and programs.
Experience of QA in a FDA regulated environment is preferred.
Experience in writing, reviewing and executing computer validation documentation (Validation Plan, IQ, OQ, PQ, RTM, summary report).
Experience in any other validations (cleaning, process, LAB instruments, manufacturing systems and others) would be a plus.
Note: 1 year contract ( Renewable)
Interested candiadtes can reach me @8951443***-Anjali
or share your CV to an**********y@Ke**********s.co .in
Job Classification
Industry: Medical, Healthcare, HospitalsFunctional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology, Role Category: Drug Regulatory Affairs/DocumentationRole: Drug Regulatory Affairs/DocumentationEmployement Type: Contract
Education
Under Graduation: Any Graduate in Any SpecializationPost Graduation: Post Graduation Not RequiredDoctorate: Doctorate Not Required