Sun Pharma- requires a Corporate Quality & Compliance Manager

Pharmaguidances; Vadodara; On-site; INR 4,200,000 - 7,200,000; Full time

Job summary

Sun Pharma in Vadodara (Gujarat) seeks a Manager – Corporate Quality & Compliance to lead investigations, CAPA verification, and global tracker management for US-market manufacturing operations. Based at Tandalja – R&D, you will drive annual trend reporting and routine dashboards with cross-functional teams.

The ideal candidate has 14–17 years in pharma quality/compliance, holds an MSc Life Sciences or B.Pharmacy, and will ensure regulatory readiness and robust CAPA processes across sites.

Qualifications

• Experience in manufacturing site catering to US Market.
• 14–17 years of experience in quality & compliance roles.
• Location: Tandalja – R&D, Sun Pharma facilities.

Responsibilities

• Investigations (Complaints, Deviations and OOS / OOT) review.
• Site visits for inspection support and CAPA verification.
• Annual trend report (Complaints, Recalls & FAR) preparation.
• Global trackers management.
• Monthly / weekly report preparation.
• Support for Complaint Log in Management.

Skills

Investigations management

CAPA verification

Regulatory inspections

Reporting

Education

M.Sc (Life Sciences)

B.Pharmacy

Job description

# Sun Pharma- requires a Corporate Quality & Compliance Manager#### *Sun Pharma- requires a Corporate Quality & Compliance Manager*Sun Pharma is India’s No. 1 pharmaceutical company and a leading global player in specialty medicines. With over 40 manufacturing facilities and a diverse portfolio, we deliver high-quality medicines across 100 countries. Driven by a commitment to innovation, we continuously strive to enhance access to medicines and improve patient care, creating better health outcomes for millions around the world.Track Biotech**Post :** Manager – Corporate Quality & Compliance**Key responsibilities :** • Investigations (Complaints, Deviations and OOS / OOT) review. • Site visits for inspection support and CAPA verification. • Annual trend report (Complaints, Recalls & FAR) preparation. • Global trackers management. • Monthly / weekly report preparation. • Support for Complaint Log in Management.**Note :** Candidate must have worked / be working in manufacturing site catering to US Market.**Additional Information** **Experience :** 14 – 17 Years **Qualification :** M.Sc (Life Sciences) / B.Pharmacy **Location** : Tandalja – R&D **Industry Type :** Pharma/ Healthcare/ Clinical research **Functional Area :** Corporate Quality & Compliance **End Date :** 30th November 2026