Analytical Chemist - GMP Compliance & Method Validation

GlaxoSmithKline Pte Ltd; Singapore; On-site; SGD 40,000 - 65,000; Full time

Job summary

GlaxoSmithKline Pte Ltd in Singapore is seeking an Analytical Chemist to support Laboratory Operations and ensure cGMP compliance for materials, samples and final products. You will help maintain data integrity, train staff, and contribute to method validation and regulatory alignment.

You will collaborate with laboratory analysts, review data with accuracy, and assist in change control, audits, and safety initiatives to uphold quality standards in a fast-paced pharmaceutical environment.

Qualifications

• Degree in chemistry with 1–4 years’ analytical experience.
• Experience in GMP/GLP environments and analytical methods.
• Familiarity with laboratory documentation and testing procedures.
• Knowledge of laboratory instrumentation and data integrity principles.
• Understanding regulatory requirements for method validation.

Responsibilities

• Collaborate with laboratory analysts to achieve department goals and provide instrumentation training.
• Ensure data accuracy supporting process and method issue resolution and support new testing technologies.
• Maintain safe lab practices and perform 6S inspections as needed.
• Assist in budgeting and resource planning for Analytical Laboratory.
• Support change assessments impacting product quality and cGMP compliance.

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

Tools

LIMS

ERP System

Job description

GlaxoSmithKline Pte Ltd in Singapore is seeking an Analytical Chemist to support Laboratory Operations and ensure cGMP compliance for materials, samples and final products. You will help maintain data integrity, train staff, and contribute to method validation and regulatory alignment.

You will collaborate with laboratory analysts, review data with accuracy, and assist in change control, audits, and safety initiatives to uphold quality standards in a fast-paced pharmaceutical environment.