Lead QC Method Development & Validation

Croda Singapore; Alabaster (AL); On-site; USD 80,000 - 120,000; Full time

Job summary

Croda Singapore is seeking a QC Specialist, Method Development and Validation to lead analytical method development, validation, transfer, and lifecycle management. You will act as the technical SME for methodologies, instrumentation, and lab investigations.

The role requires eight+ years in GMP-regulated pharma/biotech, strong ICH/Q2 knowledge, and leadership across cross-functional teams.

Qualifications

• 8+ years of GMP-regulated pharma/biotech experience.
• Strong ICH/Q2 knowledge.
• Experience leading cross-functional teams.

Responsibilities

• Lead analytical method development, validation, transfer, and lifecycle management.
• Act as SME for methodologies, instrumentation, and lab investigations.
• Partner with QA, Manufacturing, Regulatory Affairs, and external labs.

Job description

Croda is seeking a QC Specialist, Method Development and Validation to lead analytical method development, validation, transfer, and lifecycle management. You will act as the technical SME for methodologies, instrumentation, and lab investigations, partnering with QA, Manufacturing, Regulatory Affairs, and external labs.

The role requires eight+ years in GMP-regulated pharma/biotech, strong ICH/Q2 knowledge, and leadership across cross-functional teams.