of raw materials, in-process samples, finished products, and stability samples
Conduct
chemical & instrumental analysis
using HPLC, GC, UV, FTIR, dissolution, etc.
Ensure compliance with
cGMP, GLP, SOPs
, and regulatory guidelines
Prepare, review, and maintain
QC documentation
, test reports, and logbooks
Handle
OOS, OOT, deviations
, and support investigations
Assist in
method validation, verification, and transfer
activities
Support
internal and external audits
(WHO, USFDA, etc.)
Coordinate with production and QA teams for quality-related activities
Maintain laboratory instruments and ensure calibration compliance
Key Skills Required:
Strong knowledge of
pharmaceutical QC operations
Hands-on experience with
analytical instruments
Good documentation and data integrity practices
Ability to work independently and as part of a team
Interested candidates can Call / WhatsApp:
7396423749
Job Types: Full-time, Permanent
Pay: ?30,000.00 - ?52,532.26 per month
Benefits:
Food provided
Health insurance
Provident Fund
Work Location: In person
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