Job Description

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:

Provident Fund
Work Location: In person