Senior Manager - Corporate Quality Audit

Terapia - a SUN PHARMA Company; Sun City; On-site; ZAR 800,000 - 1,200,000; Full time

Job summary

A leading pharmaceutical company is seeking a Senior Manager for its Corporate Quality Audit team. This role involves performing audits across manufacturing sites to ensure compliance with regulatory standards. The ideal candidate will be an experienced professional with a pharmaceutical background, capable of leading audit initiatives to uphold the highest quality benchmarks.

Qualifications

• 18-20 years of experience in quality audit management.
• Strong understanding of regulatory standards.
• Ability to lead audit teams and manage compliance.

Responsibilities

• Conduct six system-based quality audits at manufacturing locations.
• Prepare and review audit reports within timelines.
• Categorize non-conformities and assist in compliance.

Skills

Regulatory Compliance

Audit Management

Team Leadership

Education

B. Pharm / M. Pharm Graduate

Job description

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Job Title: Senior Manager - Corporate Quality Audit

Date: Jun 30, 2025

Location: Sun House - Corporate Office

Company: Sun Pharmaceutical Industries Ltd

Job Description

Position: Sr. Manager – 1

Grade: G9

Job Location: Sun House, Mumbai

Education: B. Pharm / M. Pharm Graduate

Experience: 18-20 Years

Job Summary

• This role is part of the Corporate Quality Audits function responsible for conducting Sun site audits.
• The role involves assessing and auditing Sun manufacturing sites against current regulatory standards to ensure compliance, including adherence to applicable regulations and Sun Pharma's policies.

Key Responsibilities

• Conduct six system-based quality audits at all manufacturing locations, including sterile facilities, as per schedule.
• Prepare audit reports and review responses within specified timelines.
• Ensure audit findings are factual and compliant with regulatory requirements.
• Lead audit teams, coordinate with auditees, compile findings, and review reports.
• Categorize non-conformities into Critical, Major, and Minor.
• Assist in achieving regulatory compliance and adherence to Sun policies, including sterile manufacturing standards.
• Review and verify responses based on supporting evidence.
• Close audits after satisfactory compliance is confirmed.
• Conduct re-audits and adhoc audits as needed.
• Support pre-audit preparations and reviews at Sun sites.

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