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Lonza

Global life sciences contract manufacturer

QA Supervisor - Compliance

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeGuangzhou, Guangdong Province, ChinaNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree or higher is required.
  • At least 3 years of experience in a Quality role within the pharmaceutical industry, or at least 5 years of experience in other relevant pharmaceutical functions, is required.
  • Proficiency in written and spoken English is required.
  • Effective communication, stakeholder management, and conflict resolution skills are required.

Responsibilities

  • Conduct routine quality Gemba walks in manufacturing, warehouse, and other GMP areas to identify and communicate quality and compliance risks in a timely manner.
  • Perform on-site oversight of critical manufacturing activities, documentation practices, status labeling, material and label management, and housekeeping to promote GMP compliance; track inspection observations and coordinate timely implementation of corrective and improvement actions.
  • Analyze trends and risks identified from shop floor Gemba walks and other quality oversight activities, and drive systemic improvements to support continuous inspection readiness.
  • Promote quality culture and Data Integrity awareness to enhance compliance and inspection readiness.
  • Coordinate preparations for customer audits, regulatory inspections, corporate audits, and internal audits, including document collection, document review, on-site support, and post-audit follow-up.
  • Review audit and inspection responses and CAPA plans, track implementation of corrective actions, and drive timely closure and effectiveness verification.
  • Coordinate and complete customer questionnaires and paper assessments to ensure customer requirements are met on time.
  • Support gap analysis of new or updated regulations on site operations and coordinate related training, procedure development, and procedural updates as required.
  • Follow up on corporate audit observations and other quality system findings, and coordinate risk assessments, remediation activities, and continuous improvement initiatives with relevant functions.

About the Company

Lonza

Global life sciences contract manufacturer

Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1897

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