Posted:16 hours ago|
Platform:
On-site
Full Time
a. Responsible for issuance of BPCRs/ECRs, Protocols, Seal, Formats, Registers/Logbooks/ Bound books, Controlled / Uncontrolled copy, Controlled /Display copy of SOP, Numbering of Qualification.(IQ/OQ/PQ/RQ/DQ/URS/SAT).
b. Responsible for tracking, updating and handling of all master documents like BPCRs, ECRs, SOPs, reviewing & checking of filled BPCR/ECR, Specification, Document Archival activity.
c. Responsible for review of Raw material, Packing material, in-process, intermediate, finish, cleaning specification & test method for master after approval.
Responsible for master, issuance, tracking and retrieval of SOPs to all departments.
a. Masters in Science (Chemistry)
b. Minimum 0-1 year of work experience from pharma, preferably in quality assurance environment
Knowledge and Experience in US FDA approval, GMP compliance.
Job Type: Full-time
Pay: ₹25,000.00 - ₹400,000.00 per year
Benefits:
Work Location: In person
Vital laboratories pvt limited
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