Kerja Sepenuh Masa CQV Engineer, Gaji tinggi SGD 4,000 di AMARIS ACT PTE. LTD. Central Region (Singapore) - Maukerja

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