Pharma QA Operations & Validation Specialist

EFOR; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

EFOR in Singapore seeks a Consultant – QA Operations & Validation to support QA operations and validation in a fast-paced, regulated pharmaceutical environment. You will review records, manage deviations, and drive CAPAs while coordinating validation activities with production, engineering, and labs.

The role requires a degree in Engineering, Pharmacy, Life Sciences or equivalent, with at least 3 years in QA or Validation, strong GMP knowledge, and excellent English communication.

Qualifications

• 3+ years in QA Operations and/or Validation in pharma/biotech.
• Strong GMP and regulatory knowledge.
• Experience with batch release and deviation management.
• Proficient in validation protocols IQ/OQ/PQ.
• Excellent communication and teamwork.
• Fluent in English.

Responsibilities

• Provide on-the-floor QA Ops support to manufacturing, ensuring GMP compliance.
• Review batch records, production docs and release activities.
• Investigate deviations, non-conformities, and implement CAPA.
• Support regulatory and internal inspections and readiness activities.
• Draft, review, and approve quality and validation docs.
• Define, write, and execute IQ/OQ/PQ validation protocols for equipment/processes.
• Plan and coordinate validation activities with stakeholders.
• Perform risk assessments and contribute to change control/impact analysis.
• Support continuous improvement in QA operations and validation practices.
• Organize and lead meetings, communicate findings, and train teams.

Skills

QA Operations

Validation

GMP knowledge

Documentation

Communication

Education

Engineering degree

Life Sciences degree

Pharmacy degree

Job description

EFOR in Singapore seeks a Consultant – QA Operations & Validation to support QA operations and validation in a fast-paced, regulated pharmaceutical environment. You will review records, manage deviations, and drive CAPAs while coordinating validation activities with production, engineering, and labs.

The role requires a degree in Engineering, Pharmacy, Life Sciences or equivalent, with at least 3 years in QA or Validation, strong GMP knowledge, and excellent English communication.