Analyst, Global Stability at Endo

Tiruporur, tamil nadu, India -

Full Time

Start Date

Immediate

Expiry Date

25 Sep, 26

Salary

0.0

Posted On

27 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

HPLC, GC, UV-Vis, Dissolution, Stability Studies, OOS/OOT Investigations, cGMP, Data Integrity, LIMS, Root Cause Analysis, CAPA, Analytical Method Validation, Wet Chemistry, SOP Execution, Laboratory Documentation, Quality Control

Industry

Pharmaceutical Manufacturing

Description

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 environment. Come join us! At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.

Responsibilities

Perform routine quality control testing on raw materials, intermediates, and finished products using various instrumental and wet chemistry techniques. Execute stability studies, manage OOS/OOT investigations, and ensure strict compliance with cGMP and data integrity standards.