CQV Engineer: Pharma Equipment Qualification & Validation

AMARIS GROUP SA; Singapore; On-site; SGD 50,000 - 84,000; Full time

Job summary

Amaris Consulting is looking for a junior CQV professional to join our Life Sciences team in a pharmaceutical environment. You will support commissioning, qualification and validation activities for equipment and systems.

This role offers development in CQV, equipment qualification and computerized system validation, with collaboration across validation, engineering, quality and manufacturing. English fluency is essential. Prior GMP exposure and meticulous documentation will help you succeed.

Qualifications

• 1–3 years of experience in commissioning, qualification or validation in pharma or regulated settings.
• Experience with QC/production equipment or HVAC qualification is a plus.
• Knowledge of computerized system validation is desired.
• Familiarity with qualification documentation (protocols, tests, deviations, reports).
• Attention to detail and adherence to quality and compliance requirements.
• Ability to follow approved procedures and document work accurately.

Responsibilities

• Support commissioning, qualification and validation activities for pharmaceutical equipment and systems.
• Prepare, execute, and review qualification protocols, test scripts, and reports.
• Assist qualification of QC and production equipment, HVAC systems, and related instrumentation.
• Contribute to computerized system validation activities for equipment and validation software.
• Document testing results per approved procedures and resolve deviations.
• Collaborate with validation, engineering, quality, manufacturing, and QC teams.

Skills

CQV / qualification

GMP compliance

Documentation accuracy

Cross-functional collaboration

English fluency

Education

Bachelor's degree in Pharmaceutical Science, Life Sciences, Chemical Engineering, Biomedical Engineering, Instrumentation, Automation, or related field

Job description

Amaris Consulting is looking for a junior CQV professional to join our Life Sciences team in a pharmaceutical environment. You will support commissioning, qualification and validation activities for equipment and systems.

This role offers development in CQV, equipment qualification and computerized system validation, with collaboration across validation, engineering, quality and manufacturing. English fluency is essential. Prior GMP exposure and meticulous documentation will help you succeed.