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Location: Mumbai

Function: Global TPM QA

Reporting To: Head – TPM QA, Biosimilars

About the Prospect

This is an off-role opportunity , where you will be on the payroll of Talisman HR Solutions Pvt. Ltd.

We been associated with them as its staffing partner for over 10+ years, supporting its recruitment and staffing requirements.

Working Details

- Working Days: Monday to Friday (5 days a week)

- Working Hours: 9:00 AM to 5:00 PM

- Work Location: Mumbai, Maharashtra

- Employment Type: Full time, Off-role opportunity

- Payroll: Talisman HR Solutions Pvt. Ltd.

About the Role

We are looking for an experienced Quality Assurance professional to manage quality oversight of Third-Party Manufacturing (TPM) sites, ensuring compliance with GMP requirements, Quality Agreements, regulatory standards, and company quality policies.

Key Responsibilities

- Provide quality oversight and monitoring of Third-Party Manufacturing (TPM) sites.

- Review and approve quality documentation, including Change Controls, Deviations, CAPA, OOS, Incidents, and Risk Assessments.

- Review market complaints and significant quality events, ensuring effective Root Cause Analysis (RCA), CAPA implementation, and timely closure.

- Review APQR and prepare PQR summaries.

- Develop, review, and maintain Quality Technical Agreements (QTA) with TPM partners.

- Conduct Quality Risk Management (QRM)



and coordinate quality review meetings with TPM sites.

- Monitor TPM performance through quality scorecards, dashboards, and site assessments.

- Support First Lot Quality Reviews (FLQR).

- Represent Quality in cross-functional meetings, product launch activities, and regulatory submissions.

- Coordinate investigations and impact assessments related to temperature excursions and product quality issues.

- Ensure TPM compliance with GMP, GDP, regulatory requirements, Quality Agreements, and company quality standards.

Educational Qualification

- Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a relevant scientific discipline.

Experience & Skills

- Minimum 10 years of experience in Quality Assurance or related functions within the pharmaceutical industry.

- Experience in Third-Party Manufacturing (TPM) quality management or Supplier Quality Management preferred.

- Preferred experience in sterile dosage form manufacturing.

- Strong knowledge of GMP/GDP requirements, regulatory compliance, and pharmaceutical quality systems.

- Experience in handling deviations, CAPA, OOS, change controls, market complaints, and quality investigations.

- Excellent communication, stakeholder management, analytical, and problem-solving skills.

📌 Quality Assurance Associate | for an MNC Location - BKC (Mumbai)
🏢 Talisman HR Solutions
📍 Mumbai