Validation Engineers
Job in
El Paso, El Paso County, Texas, 88568, USA
Listed on 2026-08-21
Listing for:
QRC Group
Full Time
position Listed on 2026-08-21
Job specializations:
-
Engineering
Quality Engineering, Pharma Engineer, Biomedical Engineer, Process Engineer -
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Caguas, Puerto Rico | Posted on 08/17/2026
Weare seeking Validation Engineer professionals to support validation activities for sterile manufacturing, plant operations, facilities, equipment,systems, room requalification, and project-based validation initiatives.
Assignment may include one or more active site projects, depending on projectneed. The role includes authoring and executing protocols, supporting fieldexecution, documenting results, resolving discrepancies, and owning validationdeliverables through closeout.
- Grade DManufacturing Environment project, including Central Dust Extraction, Grade Darea/suite qualification, and equipment relocation validations.
- Bulk IPA Storagesystems validation.
- Plant operations and quality project validation scope.
- Facilities-relatedvalidations for designated engineers, including HVAC, utilities, cleanroom, andBMS.
- Author and execute commissioning and qualification protocols and reports, includingIQ/OQ/PQ.
- Own validationdeliverables through execution, discrepancy resolution, and closeout.
- Execute fieldactivities and document results in accordance with applicable validationrequirements.
- Supportequipment, systems, facilities, utilities, cleanroom, room requalification, and project validation activities as assigned.
- Performrisk-based assessments and support FMEA activities where applicable.
- Coordinatevalidation deliverables with QA, Engineering, and Manufacturing.
- Support multiple concurrent projects, depending on assignment.
- Bachelor’s degreein Engineering or a related technical field.
- Minimum 5 yearsof validation experience in a regulated environment.
- Hands-on IQ/OQ/PQauthoring and execution experience.
- Experience supporting equipment, systems, facilities, utilities, cleanroom, and/or regulated manufacturing validation.
- Working knowledge of cGMP and 21 CFR 210/211.
- Ability to workon-site in El Paso, Texas.
- Experience with Kneat.
- ISO
14971 / FMEA experience. - Cleanroom/ ISO 14644 experience.
- Validationleadership experience, where applicable.
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