Rockstone Engineering is looking for a CQV Engineer to lead the commissioning, qualification, and validation of systems and equipment in life sciences manufacturing facilities. You’ll ensure compliance with regulatory standards while supporting the delivery of high-performing, operationally ready systems.

• Develop and execute IQ, OQ, PQ protocols for systems and equipment.
• Oversee commissioning and qualification activities for utilities, equipment, and process systems.
• Ensure compliance with GxP, FDA, and EMA regulations throughout all validation stages.
• Collaborate with cross-functional teams to meet project timelines and quality standards.
• Prepare validation documentation, including protocols, reports, and traceability matrices.

• 3+ years of experience in CQV within the pharmaceutical or biotech industry.
• Strong knowledge of equipment and system qualification (utilities, HVAC, cleanrooms, etc.).
• Familiarity with regulatory requirements, including GxP, FDA, and EMA standards.
• Excellent organizational and problem-solving skills.
• Bachelor’s degree in Engineering, Life Sciences, or a related field.

• Opportunities to work with advanced automation technologies.
• Career growth in a collaborative, innovative environment.
• Competitive salary and comprehensive benefits.