CRB is seeking a highly motivated and self-driven CQV Engineer III to support the delivery and execution of Commissioning Qualification and Validation (CQV) services across Life Sciences projects. The ideal candidate will provide technical leadership and field execution support for equipment and utility systems from design through facility turnover.
This role involves guiding internal and external CQV resources coordinating with multi-disciplinary project teams and ensuring compliance with client and global regulatory requirements. The CQV Engineer II will develop and implement commissioning strategies lead verification activities and manage deliverables in alignment with project timelines and quality standards.
The position requires excellent organization communication and leadership skills as well as the ability to work collaboratively across engineering QA and construction teams in a dynamic project environment.
Define and document client requirements and develop project-specific CQV plans
Review and approve commissioning and qualification strategies for equipment and utilities
Provide input on operability maintainability and reliability considerations during design
Lead or support execution of commissioning qualification and validation activities
Witness and verify FAT/SAT test protocols and qualification execution
Provide independent verification and quality oversight of CQV deliverables
Act as the primary interface between CQV engineering and construction teams
Develop and manage CQV schedules ensuring alignment with project milestones
Support risk assessments and ensure compliance with regulatory expectations
Mentor and train junior engineers and project team members on CQV best practices
Track report and communicate CQV progress and issues to project and regional leadership
Support lessons learned and continuous improvement initiatives within the CQV organization
Qualifications :
Bachelors Degree in Engineering Architecture or Construction Management with minimum 5 years of CQV experience in the Life Sciences industry
Technical Experience:
Proven experience with commissioning and qualifications of life sciences equipment and utility systems (e.g. process equipment clean utilities HVAC WFI CIP/SIP nitrogen compressed air etc.)
Working knowledge of cGMP FDA EU and ISPE guidelines including ISPE Baseline Guide 5 and Risk-Based Approach to Commissioning and Qualification
Familiarity with URS FAT SAT IQ OQ PQ documentation and execution
Proficiency in risk assessment methodologies root cause analysis and continuous improvement tools
Skills & Attributes:
Strong interpersonal communication and presentation skills
Demonstrated leadership in coordinating cross-functional CQV efforts
Excellent technical writing and document review capability
Flexible and willing to travel as needed (50% or more)
Additional Information :
All your information will be kept confidential according to EEO guidelines.
CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity Employer and it is our policy to provide equal opportunity to all people without regard to race color religion national origin ancestry marital status veteran status age disability pregnancy genetic information citizenship status sex sexual orientation gender identity or any other legally protected category. Employment is contingent on background screening.
CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please no phone calls or emails.
CRB offers a complete and competitive benefit package designed to meet individual and family needs.
If you are unable to complete this application due to a disability contact this employer to ask for an accommodation or an alternative application process.
Remote Work :
No
Employment Type :
Full-time
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