Shift Lead - GMP Manufacturing & Team Coaching

GSK; Singapore; On-site; SGD 60,000 - 85,000; Full time

Job summary

GSK in Singapore is seeking a hands-on Shift Production Supervisor to lead a critical manufacturing shift. You will coordinate safe, compliant operations, coach operators, and resolve process and equipment issues with cross-functional teams including maintenance and quality.

You will steward documentation, drive continuous improvement and ensure adherence to GMP standards while progressing your career in a global biopharma environment.

Qualifications

• Diploma or equivalent in engineering/applied science/biotechnology or related field.
• Minimum 4 years manufacturing experience for degree holders or 7 years for diploma holders.
• Experience in a regulated manufacturing environment with knowledge of GxP.
• Strong hands-on troubleshooting skills for process & equipment issues.
• Clear written and verbal English communication for handovers and incident reporting.

Responsibilities

• Lead and coordinate shift production to meet safety, quality and output targets.
• Supervise, coach and develop operators; hold regular performance and development conversations.
• Lead first-line troubleshooting, containment and escalation for process and equipment incidents.
• Ensure compliance with site procedures, quality standards and safe work permits.
• Plan and allocate resources with maintenance, quality and technical teams to meet production needs.
• Maintain accurate shift documentation, batch records and system transactions.

Skills

Data Integrity

Detail-Oriented

Digital Fluency

Emergency Response

Financial Acumen

GxP Regulations

Lean Management

Manufacturing Processes

Problem Solving

Production Management

Project Coordination

Quality Compliance

Regulatory Compliance

Risk Awareness

Site Operations

Education

Diploma or equivalent in engineering, applied science, biotechnology or related vocational qualification

Job description

GSK in Singapore is seeking a hands-on Shift Production Supervisor to lead a critical manufacturing shift. You will coordinate safe, compliant operations, coach operators, and resolve process and equipment issues with cross-functional teams including maintenance and quality.

You will steward documentation, drive continuous improvement and ensure adherence to GMP standards while progressing your career in a global biopharma environment.