QA Supervisor, Compliance (Pharmaceutical)

TL;DR

QA Supervisor, Compliance (Pharmaceutical): Overseeing shop floor quality and inspection readiness in a GMP environment with an accent on compliance risks, data integrity, and audit coordination. Focus on driving systemic improvements, managing CAPAs, and ensuring regulatory adherence during audits.

Location: Guangzhou, China (Nansha)

Company

A global leader in life sciences and pharmaceutical manufacturing with over 30 sites across five continents.

What you will do

• Conduct routine quality Gemba walks in manufacturing and warehouse areas to identify compliance risks.
• Provide on-site oversight of critical manufacturing activities, documentation practices, and material management.
• Analyze trends from oversight activities to drive systemic improvements and ensure continuous inspection readiness.
• Coordinate preparations for customer, regulatory, corporate, and internal audits, including document review and on-site support.
• Review audit responses and CAPA plans, tracking implementation and verifying effectiveness.
• Support gap analysis of new regulations and coordinate related training and procedure updates.

Requirements

• Bachelor’s degree or above.
• At least 3 years of experience in a Quality role within the pharmaceutical industry (or 5 years in other relevant pharmaceutical functions).
• Proficient in written and spoken English.
• Strong skills in communication, stakeholder management, and conflict resolution.

Culture & Benefits

• Collaborative environment based on values of Accountability, Excellence, Passion, and Integrity.
• Opportunity to work within a globally connected team across 30+ sites.
• Inclusive culture that values diversity and unique perspectives.
• Direct involvement in manufacturing breakthrough therapies to improve millions of lives.