CQV Engineer

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