CQV Engineer - Pharma Equipment & Validation

Amaris Consulting Pte Ltd; Singapore; On-site; SGD 48,000 - 72,000; Full time

Benefits offered by this job

International community

Extensive training

Team events

ESG initiatives

Job summary

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

This role offers exposure to QC/production equipment, HVAC, and computerized system validation, with opportunities to grow in CQV, documentation, and cross-functional collaboration. Ideal candidates have a degree in relevant fields and 1–3 years of experience, fluent English, and a keen

Qualifications

• 1–3 years in commissioning, qualification, or validation within a pharmaceutical or similarly regulated environment.
• Experience with QC equipment, production equipment, or HVAC qualification is a plus.
• Knowledge or practical experience in computerized system validation is desirable.
• Strong attention to detail and good understanding of quality/compliance requirements.
• Able 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.
• Support qualification of QC equipment, production equipment, HVAC systems, and related instrumentation.
• Contribute to computerized system validation activities associated with equipment and validation software.
• Perform testing and document results in accordance with procedures.
• Identify deviations and support resolution during qualification activities.
• Ensure qualification documentation complies with GMP and data integrity requirements.
• Support performance qualification activities including process and cleaning qualification.
• Collaborate with validation, engineering, quality, manufacturing, and QC teams.
• Assist with other CQV-related activities as assigned.

Skills

CQV exposure

Validation

GMP knowledge

English fluency

Education

Degree in Pharmaceutical Science, Life Sciences, Chemical Engineering, Biomedical Engineering, Instrumentation, Automation, or a related field

Job description

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

This role offers exposure to QC/production equipment, HVAC, and computerized system validation, with opportunities to grow in CQV, documentation, and cross-functional collaboration. Ideal candidates have a degree in relevant fields and 1–3 years of experience, fluent English, and a keen