GMP QC Analyst – Analytical Methods & Validation

Confidential Careers; Singapore; On-site; SGD 60,000 - 100,000; Full time

Job summary

Confidential Careers is seeking a QC Specialist in Singapore to ensure analytical methods and testing comply with cGMP and regulatory standards. The incumbent will perform routine analytical tests for raw materials, excipients, active ingredients, intermediates and finished products, and support instrument qualification and method validation.

The role involves assisting in production process validation support, environmental monitoring, and maintaining rigorous documentation and compliance with

Qualifications

• Diploma or higher in Chemistry, Microbiology, or Pharmaceutical Sciences.
• 3–5 years of experience in a pharmaceutical GMP-regulated environment.
• Hands-on analytical testing for raw materials, APIs, excipients, packaging and finished products.
• Knowledge of FDA regulations and cGMP required.

Responsibilities

• Plan and perform analytical and microbiological testing per schedule.
• Assist instrument qualification, method validation/verification, and QA documentation.
• Support OOS investigations and debugging of analytical issues.
• Maintain laboratory housekeeping, inventory and waste disposal.
• Review and revise SOPs and testing methods to ensure GMP compliance.

Skills

Analytical testing

Microbiological testing

Troubleshooting

Regulatory knowledge

Documentation

Education

Diploma or above in Chemistry, Microbiology, Pharmaceutical Sciences

Tools

HPLC

GC

FTIR

Dissolution tester

Job description

Confidential Careers is seeking a QC Specialist in Singapore to ensure analytical methods and testing comply with cGMP and regulatory standards. The incumbent will perform routine analytical tests for raw materials, excipients, active ingredients, intermediates and finished products, and support instrument qualification and method validation.

The role involves assisting in production process validation support, environmental monitoring, and maintaining rigorous documentation and compliance with