CQV Engineer: Pharma Equipment Validation Specialist

MANTU INTERNATIONAL PTE LTD; Singapore; On-site; SGD 42,000 - 66,000; Full time

Job summary

Amaris Consulting is offering a junior CQV role in Singapore’s Life Sciences team, supporting commissioning, qualification, and validation activities for pharmaceutical equipment and systems. You will contribute to computerized system validation and performance qualification projects while collaborating with validation, engineering, quality, manufacturing, and QC teams.

The role emphasizes attention to detail, rigorous documentation, and adherence to GMP and data integrity requirements, with

Qualifications

• 1 to 3 years of experience in commissioning, qualification, or validation in pharma or regulated environments
• Experience with QC equipment, production equipment, or HVAC qualification
• Knowledge of computerized system validation
• Attention to detail and ability to document work accurately
• Fluent in English

Responsibilities

• Support commissioning, qualification, and validation activities for pharmaceutical equipment and systems
• Prepare, execute, and review qualification protocols, test scripts, and reports
• Work with interdisciplinary teams across validation, engineering, quality, manufacturing, and QC
• Identify and resolve deviations arising during qualification activities
• Ensure documentation complies with GMP and data integrity requirements

Skills

CQV

Qualification

Validation

GMP

Quality Assurance

English fluent

Education

Bachelor’s/Master’s in Pharmaceutical Science or related field

Job description

Amaris Consulting is offering a junior CQV role in Singapore’s Life Sciences team, supporting commissioning, qualification, and validation activities for pharmaceutical equipment and systems. You will contribute to computerized system validation and performance qualification projects while collaborating with validation, engineering, quality, manufacturing, and QC teams.

The role emphasizes attention to detail, rigorous documentation, and adherence to GMP and data integrity requirements, with