Qrc Group

60 Qrc Group Jobs Hiring Near You

Validation Engineer

Caguas, PR · On-site

$100 - $125/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)

Aibonito, Puerto Rico | Posted on 06/29/2026 We are seeking a Validation Specialist to support validation activities within the Injection Molding area. The selected candidate will assist in the ...

Molding Engineer

Cayey, PR · On-site

$60 - $80/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 07/07/2026 We are seeking Validation Engineer professionals to support validation activities for sterile manufacturing, plant operations, facilities, equipment ...

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 21-40

Validation Engineer

QRC Group

Caguas, PR • On-site

$100 - $125/hr

Other

Re-posted 25 days ago


Job description

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). Hands-on role focused on protocol execution, technical troubleshooting, and direct coordination with the client's team and equipment vendors.

Responsibilities
  • Develop, execute, and close IQ/OQ/PQ protocols and summary reports for manufacturing equipment and utilities.
  • Troubleshoot equipment and execution issues, determine root cause, and drive resolution to closure.
  • Work hand-in-hand with the client's engineering, quality, and manufacturing teams, and coordinate with equipment vendors/OEMs for technical support when required.
  • Support the full Validation Life Cycle: planning, URS/FRS, risk assessment (FMEA), RTM, execution, deviations, and closure.
  • Assess validation impact of equipment changes and support change control activities.
Requirements
  • Bachelor's Degree in Engineering. Required — no equivalent substitutions.
  • Minimum of five (5) years of validation experience in medical device or pharmaceutical manufacturing.
  • Hands-on equipment validation experience (IQ/OQ/PQ development and execution).
  • Proven troubleshooting capability, including direct interaction with vendors/OEMs.
  • Working knowledge of the Validation Life Cycle, cGMP, and FDA 21 CFR Part 820.
  • Strong technical writing skills. Fully bilingual (English/Spanish).
  • Availability to support production schedules, including off-shift coverage as required.
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