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.
d. 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
c. Knowledge and Experience in US FDA approval, GMP compliance.
a. Ability to work under pressure to meet specific timelines & targets
b. Strong analytical skills
c. Strong communication and collaboration skill
Pay: From ₹207,000.00 per year
Benefits:
- Leave encashment
- Provident Fund
Application Question(s):
- Where is your current location ?
- what is your current or expected ctc ?
- If selected, how soon you can join ?
Education:
Location:
- Vapi, Gujarat (Vapi) (Required)
Shift availability:
- Day Shift (Preferred)
- Night Shift (Preferred)
- Overnight Shift (Preferred)
Work Location: In person
