SUPPLIER MANAGEMENT ENGINEER

Kasmo Inc

Schaumburg, IL

JOB DETAILS
SKILLS
Biomedicine, Communication Skills, Contract Manufacturing, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Documentation, Electricity, FDA (Food and Drug Administration), Failure Mode and Effects Analysis (FMEA), ISO (International Organization for Standardization), Leadership, Manufacturing, Manufacturing Engineering, Manufacturing Operations, Mechanical Engineering, Medical Equipment, Metrics, Performance Management, Problem Solving Skills, Process Improvement, Process Validation, Product Support, Product/Service Launch, Project/Program Management, Quality Assurance, Quality Engineering, Quality Management, Request for Proposals (RFP), Research & Development (R&D), Root Cause Analysis, Supply Chain, Time Management, Value Engineering, Vendor/Supplier Evaluation, Vendor/Supplier Management, Vendor/Supplier Selection
LOCATION
Schaumburg, IL
POSTED
17 days ago

Other job titles that might work (Supplier Management, Sustaining Engineering, Supplier Quality Engineering and/or Value Engineer )

Responsible for ensuring the performance, quality, and operational readiness of contract manufacturers supporting ORS products. This role combines supplier oversight, sustaining engineering, project management, quality improvement, and new product introduction (NPI) leadership. The individual acts as a key interface between ORS internal teams and external suppliers to ensure compliant, scalable, and efficient manufacturing execution.

Job Requirements

Act as the primary operational contact for contract manufacturers.
Partner with contract manufacturers to resolve manufacturing issues.
Coordinate directly with ORS Quality and Engineering teams.
Manage supplier performance across quality, delivery, and cost metrics, and drive corrective actions.
Provide sustaining engineering support, including root cause analysis, CAPA execution, and MRB activities.
Lead supplier-related projects such as process transfers, IQ/OQ/PQ validations, and capacity expansions.
Support new product introduction through supplier selection, RFQ development, and manufacturing readiness planning.
Drive quality improvement initiatives and participate in supplier compliance activities.
Collaborate across Quality, R&D, and Supply Chain functions.

Preferred Skills

Experience in medical device or regulated manufacturing environments (FDA/ISO 13485).
Strong understanding of Device Master Records (DMR) and manufacturing documentation.
Hands-on experience with injection molding, assembly, or electro-mechanical systems.
Proficiency in quality tools such as FMEA, SPC, and problem solving.
Demonstrated project management and cross-functional leadership capabilities.
Ability to communicate effectively with suppliers and executive stakeholders.

Additional Information

Bachelor's degree in engineering (Mechanical, Manufacturing, Electrical, Biomedical, or related field).
7 10+ years of relevant experience in manufacturing engineering or supplier management.
Track record of improving supplier quality and on-time delivery performance.
Experience supporting new product launches and production transfers.

About the Company

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Kasmo Inc