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QRC Group, LLC

QRC Group, LLC

Validation Specialist

Cidra, PRIn sedeContrattoTempo pieno

Pubblicato il 6 ago 2026

Questa offerta è pubblicata in ES

Validation Specialist with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation activities (Protocols, Tests, Reports).
  • Familiarized with IQ, OQ and PQ validation phases for molds and equipment.
  • IQ: Confirmation of Drawings (including mold attributes), Equipment, and Procedures (mold setup and operating), mechanical assessment of mold and equipment.
  • Develop inspection programs and instructions for setup/positioning of tooling and parts.
  • Assuring that all product development processes and relevant applicable documentation are executed according to the agreed Product Specific Design and Development Plans.
  • Updating and defining Standard Operating Procedures (SOPs).
  • Familiarized with Gage R&R methodology preferable.
  • Preferably, familiarized with metrology equipment and methods such as calipers, micrometers, CMM, Programmable Vision Inspections Systems.

Requirements

  • Bachelor in Science
  • Experience in FDA regulated industry
  • 5 years of experience performing validation lifecycle activities
  • Technical writing skills
  • Read, write, speak and understand English and Spanish


Informazioni ruolo

Tipo di lavoro

Tempo pieno

Skill richieste

Injection Molding Process KnowledgeValidation Protocol DevelopmentIQ/OQ/PQ ValidationTechnical WritingSOP DevelopmentInspection Program DevelopmentMetrology Equipment OperationGage R&R MethodologyMechanical Assessment of ToolingFDA Regulatory ComplianceBilingual Communication (English/Spanish)Design Control Compliance

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Validation Specialist presso QRC Group, LLC a Cidra | Scovai | Scovai