We are continuously seeking skilled professionals to join our Facilities and Operations team, particularly within Reliability Engineering. This posting represents an evergreen opportunity to build a pipeline of talented CQV Engineers for current and future projects.
Key Responsibilities:
- Develop and revise qualification documents for process equipment, analytical instruments, facilities, and utility systems.
- Perform in-field execution of commissioning and qualification protocols.
- Compile complete qualification packages, including executed protocols, summary reports, and requirements traceability matrices (RTMs).
- Conduct data analysis to support recommendations included in summary reports, as needed.
- Author and execute protocols and reports for requalification activities of utility and manufacturing systems.
- Manage and resolve deviations and non-conformances related to CQV deliverables.
- Lead and drive CQV activities for assigned systems, ensuring timely completion aligned with project schedules.
- Collaborate with client stakeholders while maintaining autonomy in managing and closing CQV deliverables.
Requirements
Qualifications:
- Bachelor’s degree in Engineering, Life Sciences, or related technical discipline.
- Experience in commissioning, qualification, and validation (CQV) within GMP-regulated environments.
- Strong technical writing and documentation skills.
- Ability to work independently with minimal supervision.
- Effective communication and collaboration with cross-functional teams.
Benefits