As a Commissioning, Qualification, and Validation (CQV) Engineer at Jacobs, you will join a collaborative team focused on providing CQV support to clients in the Life Sciences sector. Your role will involve developing and executing CQV protocols while ensuring compliance with industry best practices. You will be responsible for managing CQV projects and generating technical reports. This position requires a passion for collaboration and a commitment to exceeding client expectations.

• Bachelor’s degree in Mechanical, Chemical, or Electrical Engineering or equivalent years of experience in lieu of degree
• CQV experience in the Life Sciences or advanced manufacturing industry
• Understanding of Good Manufacturing Practices (GMPs)
• Proficient with Microsoft Office – Word, Excel, PowerPoint, Project
• Flexibility and willingness to travel and work at various clients’ locations

• Develop CQV planning documents to manage CQV projects
• Generate and execute CQV protocols using Good Documentation Practices (GDPs)
• Investigate and resolve protocol exceptions or discrepancies
• Develop technical reports and CQV summary reports
• Perform risk assessments and impact assessments
• Read and verify facility and equipment drawings
• Develop Standard Operating Procedures (SOPs) and other regulatory support documentation

• Employees at Jacobs are often offered benefits designed around physical, emotional, financial and social wellbeing, including health and safety programs, mental health support, retirement and financial planning resources, flexible time off and initiatives that support a strong culture of caring.