Job Description: QA Validation Engineer (Pharmaceutical Manufacturing)

Overview

Seeking an experienced QA Validation Engineer for our pharmaceutical manufacturing team in Singapore. The role focuses on ensuring validation of equipment, processes, utilities, cleaning, and computerized systems comply with cGMP and regulatory standards. We value diversity, equity, and inclusion and welcome candidates from all backgrounds.

Key Responsibilities

• Lead validation planning and execution for equipment, processes, and computerized systems per cGMP and regulatory guidelines.
• Authorize and review IQ, OQ, and PQ protocols and reports.
• Manage deviations, CAPA, and root cause analysis to maintain compliance.
• Maintain audit-ready documentation and support regulatory inspections.
• Collaborate with cross-functional teams to sustain validated states and improve validation processes.
• Identify risks and promote continuous improvement aligned with DEI principles.

Qualifications

• Minimum 5 years in QA validation within pharmaceutical manufacturing, preferably under Singapore or similar regulations.
• Strong knowledge of cGMP, HSA, FDA, EMA regulations.
• Proven expertise in validation protocols (IQ, OQ, PQ) and computerized systems validation.
• Excellent documentation, communication, and problem-solving skills.
• Bachelor?s degree in Engineering, Pharmaceutical Science, Life Sciences, or related field is preferred.
• Commitment to fostering diversity, equity, and inclusion.

We encourage diverse applicants to join us in driving pharmaceutical quality and compliance with integrity and inclusion.

CMC operates as an employment Business and agency. No terminology in this advert is intended to discriminate on the grounds of age or experience, and we confirm that we are happy to accept applications from persons of any age or experience for this role.