: B.Sc./M.Sc. in Chemistry or B.Pharm/M.Pharm or related field
Salary
: ₹3 - 3.5 LPA
Responsibilities
:
Conduct line clearance, in-process checks, and documentation review.
Monitor adherence to SOPs, GMP, and hygiene on the production floor.
Assist in deviation handling, CAPA, and quality audits.
Review BMRs, BPRs, and cleaning records.
Support in quality risk management and change control processes.
Skills
:
Strong understanding of QA processes and documentation.
Attention to detail and team coordination.
Proficiency in MS Office tools.
Job Types: Full-time, Permanent
Pay: ₹300,000.00 - ₹350,000.00 per year
Benefits:
Leave encashment
Schedule:
Day shift
Morning shift
Supplemental Pay:
Yearly bonus
Application Question(s):
What is your Current Salary
What is your Expected Salary
Education:
Bachelor's (Required)
Experience:
CGMP: 1 year (Required)
Documentation review: 1 year (Required)
Quality assurance: 1 year (Required)
Language:
English (Required)
Hindi (Preferred)
Gujarati (Preferred)
Work Location: In person
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