Operational Quality Technician

GlaxoSmithKline; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A leading company in the healthcare sector is seeking a quality oversight professional to ensure compliance with Good Manufacturing Practices. The role involves reviewing documentation, conducting audits, and providing oversight across production and engineering teams. Ideal candidates will have a diploma in science or engineering and relevant experience in pharmaceutical processes.

Qualifications

• Minimum 3 years experience in pharma/healthcare; open to fresh graduates.
• Experience in quality and manufacturing processes.

Responsibilities

• Assess, review and approve all cGMP related documentation.
• Conduct and support site audit inspections, including internal and external audits.
• Provide quality oversight of shift operations, laboratories, and engineering teams.

Skills

Interpersonal Skills

Communication Skills

Investigative Skills

Project Management Skills

Education

Diploma in Science or Engineering

Job description

Site Name:

Singapore - Jurong

Posted Date:

May 15 2025

Purpose

To provide quality oversight for manufacturing operations and ensure full compliance with current Good Manufacturing Practices (cGMP) and regulatory requirements, so as to meet stipulated product quality standards in line with the established specifications of the organization.

Responsibilities:

1. Assess, review and approve all cGMP related documentation
2. Review batch and quality documentation to assess whether the product is fit for purpose prior to making usage decisions
3. Assess, review and approve changes that may impact product quality, validation, and cGMP compliance to ensure timely product release. Review and close changes post-implementation.
4. Inspect and release process equipment/plant after turnaround.
5. Coordinate, review, and approve periodic reviews of products, systems, and processes.
6. Conduct and support site audit inspections, including internal and external audits.
7. Draft, review, update, and serve as SME for procedures related to cGMP, site supplier management, and operational quality, ensuring compliance with cGMP and GSK standards.
8. Support shift operations across production, engineering, and laboratory teams to provide quality oversight, including change control and deviation investigations.
9. Provide quality oversight of shift operations, laboratories, and engineering teams, including regular walk-downs and coaching.

Knowledge, Skills & Experience

Professional

• Diploma in science or engineering fields
• Minimum 3 years experience in pharma/healthcare; open to fresh graduates
• Experience in quality and manufacturing processes
• Experience in pharmaceutical or healthcare sectors
• Keen on rotating 12-hour shifts

Technical

• Basic GMP knowledge
• Understanding of quality and manufacturing processes
• Knowledge of corporate management systems
• Strong audit skills
• Knowledge of equipment operations

Business

• Good interpersonal and communication skills
• Investigative skills
• Project management skills

Learn more about GSK Singapore and our people: https://www.linkedin.com/company/glaxosmithkline/life/gsksingapore