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Lonza

Global life sciences contract manufacturer

Lead Specialist, Quality Assurance

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSingaporeNo salary listedIn-person

About the Job

Requirements

  • A degree in Science, Engineering, Biotechnology, Pharmaceutical Sciences, Life Sciences, or a related discipline is required.
  • Experience in Quality Assurance within a GMP-regulated pharmaceutical, biotechnology, cell therapy, biologics, or contract manufacturing environment is required.
  • Strong knowledge of cGMP requirements, quality systems, validation, technical compliance, deviation management, CAPA, change control, and regulatory expectations is required.
  • Experience supporting regulatory inspections, customer audits, supplier audits, and quality management system activities is required.
  • Demonstrated ability to lead complex investigations, assess quality risks, make sound quality decisions, and drive issue resolution across cross-functional teams is required.
  • Strong communication, stakeholder management, project leadership, and coaching skills, with the ability to influence decisions at multiple organizational levels, are required.

Responsibilities

  • Provide Quality Assurance oversight for manufacturing, laboratory, validation, technical compliance, quality systems, and customer project activities, ensuring compliance with cGMP requirements and Lonza quality standards.
  • Lead and support complex quality events including deviations, CAPAs, change controls, customer complaints, investigations, and risk assessments using structured root cause analysis methodologies.
  • Review and approve quality documentation including SOPs, protocols, reports, batch records, validation documents, TrackWise records, and other GMP documentation to ensure accuracy and compliance.
  • Support and represent QA during regulatory inspections, customer audits, and supplier audits, acting as a subject matter expert and ensuring inspection readiness at all times.
  • Drive cross-functional quality improvement initiatives, technical projects, and operational excellence programs while providing guidance and mentorship to junior team members.
  • Provide quality oversight for product disposition, manufacturing operations, validation activities, customer projects, and quality system processes, ensuring timely execution and risk-based decision making.
  • Promote a strong culture of quality, data integrity, compliance, and continuous improvement while building effective relationships with internal and external stakeholders.

Desired Qualifications

  • Experience with electronic Quality Management Systems (eQMS), TrackWise, data integrity principles, and GMP documentation management is preferred.

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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