QG
QRC Group
Validation Engineer/Molding
Aibonito, PRSur siteContratTemps plein
Publié 23 oct. 2026
Cet emploi est publié en ES
We are seeking a Validation Specialist to support validation activities within the Injection Molding area. The selected candidate will assist in the execution, documentation, and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requirements.
Key Responsibilities
- Support the execution of validation protocols for Molding processes and equipment.
- Collect, analyze, and document validation data and results.
- Collaborate with Manufacturing, Engineering, Quality, and Validation teams to ensure project objectives are met.
- Assist in the investigation and resolution of validation-related issues, deviations, and corrective actions.
- Maintain accurate documentation in compliance with cGMP requirements and internal procedures.
- Participate in continuous improvement initiatives and provide technical support as needed.
- Ensure assigned activities are completed within established timelines and quality standards.
Requirements
- Bachelor’s degree in Engineering, Life Sciences, or a related technical field.
- Previous experience in validation activities within a regulated environment preferred (Medical Device, Pharmaceutical, or Manufacturing).
Aperçu du poste
Type de poste
Temps plein
Compétences requises
Injection Molding Process ValidationEquipment ValidationValidation Protocol ExecutionValidation Data CollectionValidation Data AnalysisValidation DocumentationcGMP ComplianceRegulatory ComplianceCross-functional CollaborationValidation Issue InvestigationDeviation and Corrective Action ManagementContinuous ImprovementProject Timeline Management
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