Quality Control Chemist

Enforce strict compliance with GMP (Good Manufacturing Practice) guidelines across all laboratory testing procedures.

Perform quality testing on raw materials, active pharmaceutical ingredients (APIs), and finished drug formulations inside the Pharma Industry.

Support both QA (Quality Assurance) audit preparation and daily QC (Quality Control) laboratory testing workflows.

Conduct advanced Analytical chemistry runs including sample assays, dissolution testing, and purity profiling.

Apply core Chemistry principles to execute physical, wet chemical, and instrumental testing procedures.

Work under the direction of the Manager Quality Control to maintain batch release schedules and laboratory compliance.

Prepare detailed batch analysis logs, stability testing summaries, and regulatory audit reports.

Bachelor's or Master's degree in Pharmacy (B.Pharm / M.Pharm), Chemistry, Analytical Chemistry, or related disciplines.

3–5 Yrs of dedicated QC laboratory experience within the pharmaceutical manufacturing sector.

Direct practical experience working under GMP compliance and pharmaceutical quality standards.

Strong structural understanding of analytical methods, wet lab chemistry, and regulatory documentation.

Systematic problem-solving mindset paired with high analytical detail orientation.