Qrc Group

31 jobs near Columbus, OH

Sr Engineer

Juncos, PR · On-site

$150 - $200/hr

Juncos, Puerto Rico We are seeking Sr Engineer with experience in Medical Devices or Pharma industry. Duties: * Develop and implement the overall Commissioning & Qualification strategy aligned with ...

Validation Engineers

El Paso, TX · On-site

$100 - $125/hr

Caguas, Puerto Rico | Posted on 08/17/2026 Weare seeking ValidationEngineer professionals to support validationactivities for sterile manufacturing, plant operations, facilities, equipment,systems ...

CSV Specialist

Vega Baja, PR · On-site

$125 - $150/hr

Vega Baja, Puerto Rico | Posted on 08/17/2026 To support the installation of several manufacturing soliddosage equipment such as but not limited to: * Encapsulator * Compression machine * Hardness ...

Sr. Engineer

Juncos, PR · On-site

$125 - $150/hr

Juncos, Puerto Rico | Posted on 08/05/2026 We are seeking a Sr. Engineer that provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational ...

Process Engineers

Caguas, PR · On-site

$80 - $100/hr

Caguas, Puerto Rico | Posted on 08/17/2026 We are seeking a Process Engineer with pharma-medical device experience aswell as validations life-cycle experience (write/execute/analyze/close) tosupport ...

Molding Engineer

Cayey, PR · On-site

$65 - $90/hr

Cayey, Puerto Rico | Posted on 08/06/2026 Molding Engineer with experience in injection molding process, workflows, and production equipment in medical devices or pharmaceutical industries.

Validation Engineers

Caguas, PR · On-site

$100 - $125/hr

Caguas, Puerto Rico | Posted on 08/17/2026 Weare seeking ValidationEngineer professionals to support validationactivities for sterile manufacturing, plant operations, facilities, equipment,systems ...

Sr Engineer

Juncos, PR · On-site

$100 - $125/hr

Juncos, Puerto Rico We are seeking Sr Engineer with experience in Medical Devices or Pharma industry. Duties: * Develop and implement the overall Commissioning & Qualification strategy aligned with ...

Aibonito, Puerto Rico | Posted on 08/25/2026 We are seeking a Validation Specialist tosupport validation activities within the Injection Molding area. The selected candidatewill assist in the ...

Validation Engineer

Caguas, PR · On-site

$80 - $100/hr

Caguas, Puerto Rico | Posted on 07/30/2026 We are seeking a Validation Engineer to support equipment validation activities in a medical device manufacturing environment (21 CFR Part 820 / ISO 13485)

Showing results 21-31

Senior Validation Engineer - Sterile Manufacturing

QRC Group

Caguas, PR • On-site

$100 - $125/hr

Other

Posted 20 days ago


Job description

Caguas, Puerto Rico | Posted on 07/07/2026

We are 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 project need. The role includes authoring and executing protocols, supporting field execution, documenting results, resolving discrepancies, and owning validation deliverables through closeout.

Project Assignment Areas
  • Grade D Manufacturing Environment project, including Central Dust Extraction, Grade D area/suite qualification, and equipment relocation validations.
  • Bulk IPA Storage systems validation.
  • Plant operations and quality project validation scope.
  • Facilities-related validations for designated engineers, including HVAC, utilities, cleanroom, and BMS.
Key Responsibilities
  • Author and execute commissioning and qualification protocols and reports, including IQ/OQ/PQ.
  • Own validation deliverables through execution, discrepancy resolution, and closeout.
  • Execute field activities and document results in accordance with applicable validation requirements.
  • Support equipment, systems, facilities, utilities, cleanroom, room requalification, and project validation activities as assigned.
  • Perform risk-based assessments and support FMEA activities where applicable.
  • Coordinate validation deliverables with QA, Engineering, and Manufacturing.
  • Support multiple concurrent projects, depending on assignment.
Requirements
  • Bachelor’s degree in Engineering or a related technical field.
  • Minimum 5 years of validation experience in a regulated environment.
  • Hands-on IQ/OQ/PQ authoring 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 work on-site in El Paso, Texas.
Preferred Qualifications
  • Experience with Kneat.
  • ISO14971 / FMEA experience.
  • Cleanroom/ ISO 14644 experience.
  • Validation leadership experience, where applicable.
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