CQV Engineer

AMARIS ACT PTE. LTD.; Singapore; On-site; SGD 40,000 - 65,000; Full time

Job summary

AMARIS ACT PTE. LTD. in Singapore seeks a junior CQV professional to support commissioning, qualification, and validation of pharmaceutical equipment and systems in a regulated environment.

You will prepare protocols, scripts, and reports; work with cross-functional teams; document deviations; and ensure GMP and data integrity. English fluency is required. Ideal candidates have 1–3 years of CQV experience in pharma, exposure to QC/production equipment or HVAC qualification, and a strong

Qualifications

• Bachelor's degree or higher in Pharmaceutical Science, Life Sciences, Chemical Engineering, Biomedical Engineering, Instrumentation, Automation, or related field.
• 1–3 years of experience in commissioning, qualification, or validation in pharma or a regulated environment.
• Experience with QC equipment, production equipment, or HVAC qualification.
• Knowledge or practical experience in computerized system validation.

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 per approved procedures.
• Identify, document, and support deviation resolution during qualification activities.
• Ensure qualification documentation complies with quality, GMP, and data integrity requirements.
• Support performance qualification activities including process, cleaning, or single-use material qualification.
• Work with validation, engineering, quality, manufacturing, and QC teams.

Skills

CQV experience

GMP knowledge

Documentation protocols

Deviations handling

Process validation

Test scripts

Cross-functional collaboration

English fluency

Education

Bachelor's in Pharmaceutical Science or Life Sciences

Tools

QC equipment

HVAC qualification

Job description

Job Description

You’ll have the opportunity to work within our Life Sciences team, supporting commissioning, qualification, and validation activities in a pharmaceutical environment. This role is ideal for junior professionals interested in developing their careers in CQV, equipment qualification, and computerized system validation.

ABOUT THE JOB

• Support commissioning, qualification, and validation activities for pharmaceutical equipment and systems
• Prepare, execute, and review qualification protocols, test scripts, and reports
• Support the 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 accurately document results in accordance with approved procedures
• Identify, document, and support the resolution of deviations arising during qualification activities
• Ensure qualification documentation complies with applicable quality, GMP, and data integrity requirements
• Support performance qualification activities, including process, cleaning, or single-use material qualification
• Work closely with validation, engineering, quality, manufacturing, and QC teams
• Support other CQV-related activities as assigned

ABOUT YOU

• Degree in Pharmaceutical Science, Life Sciences, Chemical Engineering, Biomedical Engineering, Instrumentation, Automation, or a related field
• 1 to 3 years of experience in commissioning, qualification, or validation within a pharmaceutical or similarly regulated environment
• You have between 1 and 3 years of experience in commissioning, qualification, or validation within a pharmaceutical or similarly regulated environment
• You have experience with QC equipment, production equipment, or HVAC qualification
• You have knowledge or practical experience in computerized system validation
• Experience in process validation, cleaning qualification, or single-use material qualification is an advantage
• You are familiar with qualification documentation, including protocols, test scripts, deviations, and reports
• You demonstrate strong attention to detail and a good understanding of quality and compliance requirements
• You are able to follow approved procedures and document your work accurately
• You work effectively with cross-functional stakeholders
• You are fluent in English