Job Description Summary

QC Analyst with 3–6 years of experience in pharmaceutical quality control,
skilled in routine in‑process samples, and finished products. Experienced in
instrumental analysis (HPLC, GC, UV, Dissolution), method execution as per
approved SOPs, OOS/OOT investigations, and data integrity compliance.
Well‑versed in GMP, documentation practices, and regulatory guidelines, with
strong analytical and problem‑solving skills.

Job Description

* Perform routine QC testing of raw materials, intermediates, and finished
products using approved analytical methods.
* Conduct instrumental analysis including HPLC, GC, UV–Vis, Dissolution, and
wet chemistry techniques.
* Execute stability studies, compile data, trend results, and prepare stability
reports.
* Review and ensure accuracy, completeness, and compliance of analytical data
and documentation.
* Handle OOS, OOT, deviations, and laboratory incidents, including root cause




analysis and implementation of CAPAs.
* Ensure compliance with cGMP, data integrity (ALCOA+), SOPs, and regulatory
guidelines.
* Support method transfers, method verifications, and analytical method
validations as required.
* Maintain laboratory equipment, perform calibrations, and ensure proper
documentation of laboratory activities.
* Participate in internal audits, regulatory inspections, and continuous
improvement initiatives.
* Coordinate with cross‑functional teams such as QA, Manufacturing, and
Regulatory Affairs as needed.

* Proficiency in laboratory documentation and electronic systems (LIMS
preferred).
* Good problem‑solving, analytical, and communication skills.
* Ability to work independently as well as collaboratively in a regulated
workplace.

📌 Analyst, Global Stability (Thiruporur)
🏢 Endo
📍 Thiruporur