CQV Engineer — Pharma Equipment Validation & Growth

Amaris Consulting

Singapore

On-site

SGD 42,000 - 65,000

Full time

14 days+

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Job summary

Amaris Consulting is seeking a CQV junior professional to support commissioning, qualification and validation activities in a pharmaceutical environment. You will prepare protocols, execute tests, review reports, and document results following approved procedures.

You will work with cross-functional teams including validation, engineering, quality and manufacturing, ensuring data integrity and GMP compliance while developing your career in CQV and related systems.

Qualifications

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.
Experience with QC equipment, production equipment, or HVAC qualification or knowledge of 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 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 document results in accordance with approved procedures.
Identify, document, and support resolution of deviations arising during qualification activities.
Ensure qualification documentation complies with quality, GMP, and data integrity requirements.
Work closely with validation, engineering, quality, manufacturing, and QC teams.
Support other CQV-related activities as assigned.