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