Supplier Quality Engineer II - Medical Devices (Hybrid)

Pharmavise Corporation; Saint Paul (MN); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Pharmavise Corporation in Arden Hills, MN seeks a Supplier Quality Assurance Engineer II for a hybrid role focused on improving supplier quality and regulatory compliance in medical devices.

The role collaborates with cross-functional teams to resolve supplier-related challenges and supports global quality systems. Candidates should have a BS in engineering and 2–3 years in quality/risk management.0Schedule: 3 days onsite; 08:00–16:30.

Qualifications

• BS degree in an Engineering related field (Mechanical/Materials/Chemical/Electrical) with 2-3 years related experience.
• Experience in Quality Management Systems, regulatory compliance, and risk management.
• Experience with problem solving quality tools, CAPA, Technical Documentation

Responsibilities

• Drives improvement and corrective actions in quality of components sourced from outside suppliers.
• Assess & drive reactive as well as proactive supplier investigations with cross-functional teams.
• Develops solutions to complex problems; evaluates factors and applies applicable policies and methods.
• Plans and organizes non-routine tasks; manages project schedules and priorities.
• Interacts with suppliers; may lead projects within the function and influence senior management decisions.
• Maintains patient safety and product quality by complying with Quality Policy and Quality Systems.

Skills

Quality Mgmt Systems

Regulatory compliance

Risk management

CAPA

Problem solving

Technical Documentation

Education

BS in Engineering

Job description

Pharmavise Corporation in Arden Hills, MN seeks a Supplier Quality Assurance Engineer II for a hybrid role focused on improving supplier quality and regulatory compliance in medical devices.

The role collaborates with cross-functional teams to resolve supplier-related challenges and supports global quality systems. Candidates should have a BS in engineering and 2–3 years in quality/risk management.0Schedule: 3 days onsite; 08:00–16:30.