Process Validation Engineer - Medical Device jobs in United States
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Gandiv Insights LLC ยท 1 day ago

Process Validation Engineer - Medical Device

Gandiv Insights LLC is seeking a Process Engineer to support medical device manufacturing operations. The role involves developing, optimizing, and validating manufacturing processes while collaborating with various teams to ensure compliance and efficiency in a GMP-regulated environment.

Information Technology & Services

Responsibilities

Develop, optimize, and maintain manufacturing processes for medical devices
Support process characterization and process validation (IQ/OQ/PQ) activities
Identify and implement process improvements to enhance yield, efficiency, and product quality
Support new product introductions (NPI) and technology transfer to manufacturing
Create and maintain process documentation, work instructions, and SOPs
Collaborate with R&D, Manufacturing, Validation, and Supply Chain teams
Troubleshoot manufacturing issues using root cause analysis and implement corrective actions
Ensure compliance with FDA 21 CFR 820, ISO 13485, and internal quality standards

Qualification

Process ValidationProcess EngineeringGMP RegulationsFDA 21 CFR 820ISO 13485Root Cause AnalysisContinuous ImprovementSOP DevelopmentNPITechnology Transfer

Required

Bachelor's degree in Mechanical, Manufacturing, Biomedical Engineering, or related field
4+ years of experience in medical device manufacturing or process engineering
Hands-on experience with process validation and equipment qualification
Strong understanding of GMP and medical device regulations
Excellent problem-solving and documentation skills

Company

Gandiv Insights LLC

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Gandiv Insights is a leading professional services and staffing firm specializing in top-tier personnel and technical solutions across engineering, IT, non-IT, and healthcare sectors.

Funding

Current Stage
Growth Stage
Company data provided by crunchbase