Process Engineer I: Manufacturing Process & Validation

Quality Consulting Group, LLC; Humacao (PR); On-site; USD 70,000 - 110,000; Full time

Job summary

Quality Consulting Group, LLC is seeking a talented engineer to join our team in Puerto Rico and the USA. The role focuses on technical and sustaining engineering support in a manufacturing setting with emphasis on validation for medical devices.

You will lead process improvements, collaborate with cross-functional teams, and implement equipment and methods that meet quality standards. Shift availability may be required for first and second shifts.

Qualifications

• Bachelor's degree in the specified engineering fields.
• 3+ years of validation experience.
• Knowledge of validations in a medical devices environment.
• Able to collaborate with cross-functional teams on solutions.
• Strong problem-solving skills and attention to detail are essential.
• Willingness to work first and/or second shift if required.

Responsibilities

• Provides technical and sustaining engineering support in a manufacturing area.
• Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies.
• Integrates equipment and material capabilities to meet process specifications.
• Reviews product development requirements for compatibility with processing methods to determine costs and schedules.
• Interacts with design and development to ensure processes and designs are compatible.
• May develop and conduct statistical analysis to document work.
• Leads development/optimization of new manufacturing concepts and transfer to operations.
• Develops manufacturing processes applicable to SPC and measurement systems.
• Ensures processes comply with regulations.

Skills

Cross-functional collaboration

Problem solving

Attention to detail

Shift flexibility

Education

Bachelor's degree in Mechanical/Biomedical/Industrial/Chemical Engineering

Job description

Quality Consulting Group, LLC is seeking a talented engineer to join our team in Puerto Rico and the USA. The role focuses on technical and sustaining engineering support in a manufacturing setting with emphasis on validation for medical devices.

You will lead process improvements, collaborate with cross-functional teams, and implement equipment and methods that meet quality standards. Shift availability may be required for first and second shifts.