Analytical Lab Systems & Equipment Lead

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

Job summary

GlaxoSmithKline is seeking an Analytical Equipment Validation Specialist in Singapore to ensure installation, validation, calibration and maintenance of analytical equipment and computer systems in quality laboratories in line with QMS standards and regulatory requirements.

The role includes leading investigations, performing validation reviews, updating procedures, and training staff to maintain cGMP compliance and high data integrity across the lab environment.

Qualifications

• Science degree (or Diploma) with extensive >5 years in Chemical, Pharma or Manufacturing industries.
• Strong knowledge of GxP and laboratory equipment validation.
• Experience with regulatory expectations (ATS/ICH) and laboratory compliance.

Responsibilities

• Maintain and calibrate analytical equipment in line with site procedures and regulations.
• Lead and participate in investigations arising from equipment or computer system events; propose CAPA.
• Perform periodic validation reviews and recommend re-validation as needed.
• Lead or support equipment validation activities, including documentation review and approvals.
• Maintain computer systems and lab equipment per change and access controls.
• Assess impacts of changes to equipment/systems and update related documentation promptly.
• Update laboratory procedures to comply with regulatory and QMS requirements.
• Ensure safe lab environment and conduct 6S inspections.
• Provide training to staff on systems/equipment and procedures.
• Ensure timely Pharmacopoeia & ATS reviews.

Skills

Data Integrity

Digital Fluency

GxP Regulations

Quality Assurance

Quality Control

Risk Awareness

Testing Operations

Lean Management

Problem Solving

Detail-Oriented

Education

Science degree/ Diploma with >5 years in Chemical/ Pharma/ Manufacturing

Job description

GlaxoSmithKline is seeking an Analytical Equipment Validation Specialist in Singapore to ensure installation, validation, calibration and maintenance of analytical equipment and computer systems in quality laboratories in line with QMS standards and regulatory requirements.

The role includes leading investigations, performing validation reviews, updating procedures, and training staff to maintain cGMP compliance and high data integrity across the lab environment.