Pharma Manufacturing Operations Engineer — Process Improvement

GlaxoSmithKline; Singapore; On-site; SGD 70,000 - 110,000; Full time

Job summary

GlaxoSmithKline in Singapore is seeking a qualified manufacturing professional to lead deviation investigations, CAPA and process improvements on-site at the Singapore facility.

You will collaborate across manufacturing, quality, MSAT and maintenance, driving data-driven decisions, supporting validation, trials and tech transfers, and ensuring safe, compliant production with timely issue resolution.

Qualifications

• Bachelor’s degree in engineering, biotechnology, chemical engineering, life sciences or related discipline.
• Minimum 4 years of relevant experience in regulated manufacturing such as pharmaceutical, biotech or chemical production.
• Practical experience in deviation investigation, root cause analysis and CAPA management.
• Strong troubleshooting skills for process and equipment issues.
• Working knowledge of current good manufacturing practices and quality systems.

Responsibilities

• Lead and manage complex deviation investigations and corrective actions to timely closure.
• Design and deliver process improvement projects to increase yield, reduce variability or raise efficiency.
• Support validation, trials and technical transfer activities to enable smooth production start-up.
• Monitor process parameters and trends, and support risk assessments for quality and business continuity.
• Prepare clear technical documents, training materials and work instructions for operations teams.
• Build strong working relationships with manufacturing, quality, MSAT and maintenance to meet production goals.

Skills

Deviation investigations

Root cause analysis

CAPA management

Troubleshooting

Quality systems

Data analysis

Communication

Education

Bachelor’s degree in engineering, biotechnology, chemical engineering, life sciences or related discipline

Tools

SAP

Manufacturing execution systems

Electronic batch records

Job description

GlaxoSmithKline in Singapore is seeking a qualified manufacturing professional to lead deviation investigations, CAPA and process improvements on-site at the Singapore facility.

You will collaborate across manufacturing, quality, MSAT and maintenance, driving data-driven decisions, supporting validation, trials and tech transfers, and ensuring safe, compliant production with timely issue resolution.