Analytical Chemist I - GMP Method Development & QC

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

Job summary

GSK in Singapore is seeking an experienced analytical professional to draft, compile, review and update laboratory documents including analytical methods and validation reports, supporting GMP and the lab’s operating framework.

You will ensure data accuracy, contribute to new testing technologies, maintain safe lab practices, participate in investigations, and manage change control to protect product quality.

Qualifications

• Minimum 3–5 years in an analytical environment, preferably in the pharmaceutical or regulated industry.
• Good knowledge of GMP.
• Understanding product specification and method analysis.

Responsibilities

• Draft, compile, review and update laboratory documents such as analytical methods, specifications, validation/equivalency protocols and local procedures.
• Ensure data supporting resolution of process and method issues is accurate for correct actions.
• Contribute to plans for new or improved testing technologies and methods for products or cleaning processes.
• Maintain a safe lab environment through safety risk assessments and 6S inspections.
• Lead or participate in investigations from laboratory incidents and assess impact to recommend remedial or CAPA actions.
• Own and support initiation and progression of changes affecting product quality, validation, or cGMP compliance; coordinate testing and ensure closure of changes.

Skills

Data Integrity

Detail-Oriented

Digital Fluency

GxP Regulations

Lean Management

Problem Solving

Quality Assurance

Quality Control

Risk Awareness

Testing Operations

Tools

Laboratory instrumentation

Job description

GSK in Singapore is seeking an experienced analytical professional to draft, compile, review and update laboratory documents including analytical methods and validation reports, supporting GMP and the lab’s operating framework.

You will ensure data accuracy, contribute to new testing technologies, maintain safe lab practices, participate in investigations, and manage change control to protect product quality.