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Engineer CQV_BLS

Exyte
Dallas, USA
Temporary
Mid-Senior
Onsite
Discovered 3 weeks ago
Commissioning and system completionBLS / pharmaceutical projectsCQVHVAC/BMS, mechanical utilities, electrical, instrumentation, or controlscGMPGood Documentation Practices and data integrity

Full Job Posting

Role overview

Executes and documents system-level commissioning for BLS/pharmaceutical projects, preparing facilities, utilities, equipment, and controls for safe turnover.

Reports to the Commissioning Manager and works with engineering, construction, quality, EHS, subcontractors, OEMs, and client CQV/validation representatives.

Qualification or validation protocols are supported or executed only when assigned and approved by the client and project leadership.

Commissioning and turnover

  • Plans and executes assigned system commissioning and verifies construction and Mechanical Completion readiness.
  • Coordinates pre-commissioning, vendor start-up, calibration, loop checks, functional testing, and performance verification.
  • Develops work plans, procedures, check sheets, test scripts, and commissioning records; reviews relevant drawings and vendor documents.
  • Supports system boundaries, tagging, walkdowns, turnover sequencing, and commissioning schedule development.
  • Performs or witnesses completion checks, cleaning, pressure/leak testing, energization, calibration, balancing, start-up, and testing as applicable.
  • Coordinates field teams and confirms permits, risk assessments, LOTO, energization controls, temporary utilities, and safe-work prerequisites.
  • Records test evidence, identifies deficiencies and deviations, supports root-cause evaluation and retesting, and maintains completions-system status.
  • Compiles turnover packages and supports FAT/SAT, vendor coordination, training, O&M documentation, and client handover.

Required qualifications

  • Bachelor’s degree in a relevant engineering discipline or equivalent relevant technical experience.
  • 5+ years of commissioning, start-up, field engineering, or CQV experience, including regulated life-science facility experience.
  • Hands-on experience in at least one relevant discipline, including HVAC/BMS, utilities, electrical, instrumentation, or controls/automation.
  • English proficiency; safety-focused execution and disciplined documentation.

Preferred qualifications and capabilities

  • Greenfield or brownfield project experience, including work in or adjacent to operating GMP facilities.
  • Relevant commissioning, controls, electrical, mechanical, or CQV certification or training; electronic completions or digital turnover experience.
  • Working knowledge of cGMP, documentation and data-integrity practices, risk-based verification, and the qualification/validation interface.
  • Ability to interpret technical drawings and documents, write test records, troubleshoot systems, and coordinate field work.

Work setting

  • Project-site assignment with travel to vendors, fabrication facilities, or other project locations as required.
  • Extended on-site periods and work outside normal hours may be needed during critical testing, start-up, and turnover windows.

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