Conduct analysis of raw materials, in-process samples, finished products, and stability samples.
Perform analytical tests using HPLC, UV, FTIR, Dissolution, GC, and other instruments as per specifications and SOPs.
Prepare and review analytical reports, COAs, and ensure timely documentation.
Ensure compliance with cGMP, GLP, and regulatory requirements.
Support method validation and transfer activities.
Maintain laboratory records, equipment calibration, and sample management.
Participate in investigations of OOS/OOT results and deviations.
Handle audit queries and support in regulatory inspections (USFDA, MHRA, etc.).
Requirements:
Only male candidates are eligible for this position.
Must have experience in
formulations (oral solid dosage or other)
in a regulated environment.
Sound knowledge of
regulatory guidelines
and
documentation practices
.
Proficiency in operating analytical instruments.
Strong communication, teamwork, and analytical skills.
Willing to work in shifts if required.
Interested can call/ WhatsApp: 7396423749.,
Job Types: Full-time, Permanent
Pay: ?25,000.00 - ?60,000.00 per month
Benefits:
Health insurance
Provident Fund
Work Location: In person
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