QC - Assistant Manager

PeopleStrong; Daman; On-site; INR 600,000 - 900,000; Full time

Job summary

PeopleStrong is seeking a Quality Control professional to oversee the QC Raw Material section, manage work allocation and shifts, and ensure timely testing and release of APIs, excipients, and packaging materials to support production schedules.

You will review analytical data and chromatograms from instruments such as HPLC, GC, FTIR, UV-Vis, Karl Fischer and Auto-Titrators for accuracy and compliance, lead OOS/OOT investigations, CAPA, and change controls with strict data integrity (ALCOA+) in

Qualifications

• Postgraduate qualification in Pharmacy or Science.
• Experience in QC operations for APIs/excipients is preferred.

Responsibilities

• Oversee daily operations of the QC Raw Material section and plan shifts.
• Review analytical test data, chromatograms, and audit trails for accuracy and compliance.
• Lead laboratory investigations for OOS/OOT and implement CAPAs and change controls.

Skills

Laboratory management

QA & compliance

Data integrity

Analytical testing

ALCOA+

Education

Post graduate

M.Sc. / M. Pharm

Tools

HPLC

GC

FTIR

UV-Vis

Karl Fischer

Auto-Titrators

Empower 3

Job description

Quality Control (QC) QC HPLC IR Titration GC Analysis

Post Graduate

M.Sc. M. Pharm

CERTIFICATION

Working Language

Job Description

Laboratory Management: Oversee the daily operations of the QC Raw Material section, including work allocation, shift planning, and ensuring the timely testing and release of APIs, excipients, and packaging materials to support production schedules.

Data Review & Approval: Perform secondary review of analytical test data, chromatograms, and audit trails generated from sophisticated instruments (HPLC, GC, FTIR, UV-Vis, Karl Fischer, Auto-Titrators) for accuracy and compliance.

QMS & Investigations: Lead laboratory investigations for Out of Specification (OOS), Out of Trend (OOT), and routine deviations. Implement effective Corrective and Preventive Actions (CAPA) and evaluate change controls related to the RM section.

Compliance & Data Integrity: Ensure strict adherence to ALCOA+ principles and Data Integrity guidelines across all laboratory operations. Monitor electronic data systems (e.g., Empower 3) and ensure contemporary documentation practices.