Posted:2 months ago|
Platform:
On-site
Full Time
Key Responsibilities
Conduct testing of raw materials, in-process samples, and finished products per pharmacopeial guidelines (IP/BP/USP/Ph. Eur.).
Perform assays, dissolution, impurity profiling, and other pharmacopeial tests.
Carry out wet chemistry procedures, including pH and conductivity testing.
Operate and calibrate analytical instruments (IR, FTIR, etc.).
Ensure compliance with GMP, GLP, and SOPs.
Maintain accurate documentation: test reports, calibration logs, change controls, etc.
Collaborate with QA and Production teams.
Support audit readiness and participate in internal/external audits.
Handle sample collection, labeling, storage, and assist with stability studies
Candidate Requirements Education (Preferred):
B.Sc/ M.Sc in Chemistry
B.Pharm / M.Pharm (Pharmaceutical Chemistry) Experience:
3–5years in a pharmaceutical or regulated manufacturing setup
Prior work in sterile/medical device/cleanroom environments is essential
Technical Skills:
Proficient in pharmacopeial testing and documentation
Skilled with IR Spectroscopy, FTIR, pH/conductivity meters
Familiar with method validation and instrument calibration
Strong understanding of GMP, data integrity, and cleanroom compliance
Job Type: Full-time
Pay: ₹212,610.52 - ₹580,020.88 per year
Work Location: In person
Talencia Integrated solutions
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2.12611 - 5.80021 Lacs P.A.
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