QA Operations Lead - cGMP, Compliance & Audit Readiness

No deviation; Singapore; On-site; SGD 60,000 - 100,000; Full time

Job summary

No Deviation is seeking a QA Operations Executive to provide quality assurance oversight across manufacturing and QC activities under cGMP. The role ensures product quality, regulatory adherence, and continuous improvement of the Quality Management System while supporting batch disposition, deviations, CAPA, and change controls.

Applicants should have a Life Sciences/Engineering/Pharma background with at least 2 years in QA within regulated industries, strong GMP knowledge, and experience with

Qualifications

• Bachelor's degree in Life Sciences, Pharmacy, Engineering, Chemistry, or related technical discipline.
• Minimum 2 years of QA experience in regulated life sciences industries.
• Strong knowledge of GMP, cGMP, and regulatory requirements.
• Experience with Quality Management Systems (QMS) and documentation review.

Responsibilities

• Provide QA oversight to ensure cGMP compliance across Manufacturing and QC operations.
• Manage deviations, investigations, CAPAs, change controls, and risk assessments.
• Authorize quality-related activities including release decisions and Quality Tag Outs.
• Review GMP documentation including SOPs, Master Batch Records, and QC reports.
• Support audits, inspections, and quality risk assessments.
• Identify compliance gaps and drive continuous quality improvement within QMS.

Skills

GMP Knowledge

QMS Experience

CAPA

Deviation Mgmt

Documentation Review

Root Cause

Risk Assessment

Regulatory Compliance

Cross-functional

Audit Readiness

Education

Bachelor's degree in Life Sciences, Pharmacy, Engineering, Chemistry, or a related technical discipline

Tools

QMS (Quality Management System)

Job description

No Deviation is seeking a QA Operations Executive to provide quality assurance oversight across manufacturing and QC activities under cGMP. The role ensures product quality, regulatory adherence, and continuous improvement of the Quality Management System while supporting batch disposition, deviations, CAPA, and change controls.

Applicants should have a Life Sciences/Engineering/Pharma background with at least 2 years in QA within regulated industries, strong GMP knowledge, and experience with