Analytical Development Scientist — GMP & Validation Focus

GlaxoSmithKline; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

GlaxoSmithKline is seeking a Laboratory Specialist in Singapore to draft, review and update GMP-related documents, ensuring data accuracy for issue resolution. The role supports new testing technologies and safe lab operations, including investigations and CAPA actions to protect product quality.

Candidates should have a chemistry degree and 3+ years in analytics within regulated environments. The position emphasizes data integrity, regulatory compliance, and cross-functional collaboration to

Qualifications

• Open to fresh graduates with a minimum degree in chemistry or related field.
• Minimum 3 years experience in an analytical environment, preferably in the pharmaceutical or regulated industry.
• Good knowledge of GMP.
• Understanding product specification and method analysis.
• Knowledge of laboratory instrumentation.
• Laboratory support procedures.
• Regulatory requirements for method validation.
• Good communication skills.
• Problem solving skills.
• Project management skills.

Responsibilities

• Draft, compile, review and update laboratory documents related to GMP and laboratory framework.
• Ensure data supporting issue resolution is accurate for correct action.
• Contribute to plans for implementing new/improved testing technologies or methods.
• Ensure a safe lab environment through risk assessments and 6S inspections.
• Lead or participate in investigations and assess impact for CAPA actions.
• Support change initiation and progression impacting product quality or validation; coordinate testing and comment on changes.
• Review and ensure closure of changes upon completion.

Skills

Data Integrity

Detail-Oriented

Digital Fluency

GxP Regulations

Lean Management

Problem Solving

Quality Assurance

Quality Control

Risk Awareness

Testing Operations

Education

Degree in chemistry or related field

Tools

Laboratory instrumentation

Job description

GlaxoSmithKline is seeking a Laboratory Specialist in Singapore to draft, review and update GMP-related documents, ensuring data accuracy for issue resolution. The role supports new testing technologies and safe lab operations, including investigations and CAPA actions to protect product quality.

Candidates should have a chemistry degree and 3+ years in analytics within regulated environments. The position emphasizes data integrity, regulatory compliance, and cross-functional collaboration to