Laboratory Analytics & Equipment Specialist

Wood; Singapore; On-site; SGD 50,000 - 80,000; Full time

Benefits offered by this job

Meaningful projects

Diversity and inclusion

Competitive salary

Professional development

Global connections

Job summary

Wood is seeking a Laboratory Analytical Support Officer to join our Singapore operations. The role ensures analytical equipment and computer systems in the quality laboratories are installed, validated, calibrated and maintained per QMS standards and regulatory guidelines.

Responsibilities include leading investigations, performing periodic validation reviews, and maintaining change controls. The position emphasizes safety, CAPA, and ongoing training to uphold cGMP and pharmacopoeia standards.

Qualifications

• Strong communication skills, both written and spoken.
• Knowledge of GxP and laboratory equipment/validation.
• Familiarity with quality control and laboratory environments.

Responsibilities

• Ensure analytical equipment is maintained and calibrated on time per procedures and regulatory requirements.
• Lead or participate in investigations of equipment/systems events and implement CAPA.
• Perform periodic validation reviews and advise on re-validation as needed.
• Oversee validation activities including documentation generation and approval.
• Maintain computer systems and laboratory equipment under change and access controls.
• Assess impacts of changes to ensure all areas are updated and compliant.
• Revise lab procedures to meet regulatory and QMS requirements.
• Maintain a safe working environment and conduct HSE inspections.

Skills

Communication skills

GxP knowledge

Laboratory environment knowledge

Education

Science degree

Job description

Wood is seeking a Laboratory Analytical Support Officer to join our Singapore operations. The role ensures analytical equipment and computer systems in the quality laboratories are installed, validated, calibrated and maintained per QMS standards and regulatory guidelines.

Responsibilities include leading investigations, performing periodic validation reviews, and maintaining change controls. The position emphasizes safety, CAPA, and ongoing training to uphold cGMP and pharmacopoeia standards.