Supplier Quality & Manufacturing Engineer I

Cook Medical; Bloomington (IN); On-site; USD 70,000 - 110,000; Full time

Job summary

Cook Inc - Bloomington in Bloomington, IN, is seeking a Manufacturing Engineer 1, Supplier to plan, direct, and lead supplier controls and manufacturing processes for medical device products.

You will coordinate cross‑functional change plans with suppliers, address incoming quality control issues, and drive multiple projects to timely completion while maintaining safety, quality, and regulatory compliance. Collaboration with global teams is essential.

Qualifications

• Bachelor's degree in Engineering.
• Experience using analytical skills and problem solving.
• Ability to understand business software applications.
• Working knowledge of manufacturing and production processes.
• Excellent communication across diverse teams.

Responsibilities

• Coordinate with cross-functional teams to create and execute change plans for supplier changes in compliance with Cook QMS and regulatory requirements.
• Evaluate, document and resolve incoming quality control non-conformances and supplier discrepancies.
• Lead multiple projects concurrently with effective communication to minimize impact to manufacturing.
• Maintain training requirements and seek opportunities for growth.
• Interact professionally with global organization levels and uphold safety standards.
• Maintain regular attendance and deliver quality results.
• Communicate effectively in collaborative and independent environments with minimal supervision.
• Stay calm in fast-paced situations.

Skills

Analytical skills

Problem solving

Communication

Manufacturing knowledge

Cross-functional collaboration

Education

Bachelors in Engineering

Tools

Microsoft Word

Microsoft Excel

Microsoft Project

Microsoft Outlook

JBase

Livelink

Engineering Server

Business Objects

Job description

Cook Inc - Bloomington in Bloomington, IN, is seeking a Manufacturing Engineer 1, Supplier to plan, direct, and lead supplier controls and manufacturing processes for medical device products.

You will coordinate cross‑functional change plans with suppliers, address incoming quality control issues, and drive multiple projects to timely completion while maintaining safety, quality, and regulatory compliance. Collaboration with global teams is essential.