Senior Medical Device Engineer - Process & Product Lead

Veg Group; Aibonito (PR); On-site; USD 110,000 - 160,000; Full time

Job summary

Validation & Engineering Group, Inc. is seeking a Principal Engineer to provide technical leadership and support for Medical Devices manufacturing processes and product activities at our designated facility.

You will lead process improvements, troubleshoot manufacturing challenges, collaborate with Quality, Manufacturing and Validation teams, and drive regulatory compliance and continuous improvement initiatives across cross-functional teams.

Qualifications

• Bachelor’s degree in Engineering or a related technical discipline is required.
• Strong analytical, troubleshooting, problem-solving, and communication skills are a must.
• Ability to work effectively with cross-functional teams and manage multiple priorities.
• Experience in a regulated manufacturing environment, preferably medical devices, is preferred.

Responsibilities

• Provide technical guidance and engineering support for manufacturing processes and product-related activities.
• Lead process improvement initiatives to enhance product quality, operational efficiency, and manufacturing performance.
• Troubleshoot technical issues and support investigations related to manufacturing processes, equipment, and product performance.
• Collaborate with Quality, Manufacturing, Validation, and other cross-functional teams to resolve technical challenges.
• Support the development, implementation, and optimization of engineering procedures, processes, and technical documentation.
• Ensure engineering activities comply with applicable regulatory requirements, quality standards, and company procedures.

Skills

Analytical skills

Troubleshooting

Cross-functional teamwork

Regulatory awareness

Education

Bachelor's degree in Engineering

Job description

Validation & Engineering Group, Inc. is seeking a Principal Engineer to provide technical leadership and support for Medical Devices manufacturing processes and product activities at our designated facility.

You will lead process improvements, troubleshoot manufacturing challenges, collaborate with Quality, Manufacturing and Validation teams, and drive regulatory compliance and continuous improvement initiatives across cross-functional teams.