Manager

We are seeking a highly competent professional with expertise in Quality Control investigations and pharmaceutical laboratory operations.

Role Overview
The incumbent will be responsible for supporting site quality investigations related to OOS, OOT, deviations, market complaints, and other non-conformities, while ensuring compliance with regulatory expectations and internal quality systems.

Required Skills & Experience
Strong knowledge of laboratory testing for sterile and oral solid dosage forms
Good understanding of laboratory practices and QC instruments with troubleshooting expertise
Experience in handling and investigating non-conformities
Proficiency in RCA, CAPA, and investigation documentation/review
Good understanding of GLP, GMP, GDP, and overall GxP compliance
Working knowledge of Veeva Vault, eDMS, SAP

Key Responsibilities
Conduct and support investigations for quality events across the site
Collaborate with CFTs and operational teams to identify root cause and define CAPA
Provide investigation-related support during regulatory, vendor, third-party, and customer audits
Support investigation teams across sites for audit readiness and response activities

Diversity Hiring Note
As part of our commitment to building a more inclusive workplace, women professionals are especially encouraged to apply.