Quality Inspector I

Medical Murray•Lake Zurich, IL

3d•$18 - $23•Onsite

About The Position

Founded in 1996, Medical Murray is a privately owned medical device company specializing in the development, testing, and manufacturing of finished devices, components, and subassemblies. We partner with clients ranging from innovative startups to the world’s largest OEMs. Our expertise includes permanent implants, delivery systems, and complex catheters for vascular, gastrointestinal, urologic, and other interventional markets. Our culture is driven by five core values: Helpful, Happy, Personal Responsibility, Trustworthy and Clever & Skillful. These principles guide our work, our relationships, and our commitment to improving patient outcomes worldwide. As a Quality Inspector I, you will perform component, in-process, and final inspections within a regulated manufacturing environment. This role plays a critical part in confirming that materials and finished products meet customer specifications, engineering drawings, and quality standards. You will work closely with Production, Engineering, and Quality teams to identify defects, support investigations, and maintain compliance with established procedures. This position is ideal for experienced inspectors who enjoy hands-on quality work, working under microscopes, and supporting high-quality manufacturing outcomes.

Requirements

High School Diploma or equivalent required
1-3 years of inspection experience required
Computer proficiency required for data entry and business system tracking
Experience using metrology tools such as: Calipers, Micrometers, Vision measurement systems, Inspection microscopes, Other measurement instrumentation
Ability to read and interpret engineering drawings
Strong manual dexterity and hand-eye coordination
Experience completing inspection documentation and reports
Ability to write procedures and maintain accurate records
Strong organizational and time management skills
Good judgment and attention to detail
Proficiency with Microsoft Office (Word, Excel)
Experience working with Adobe/PDF documentation
Ability to work within quality tracking systems

Nice To Haves

Medical device or regulated manufacturing experience preferred
Strong attention to detail and precision mindset
Experience in regulated manufacturing environments
Ability to proactively identify quality risks
Strong communication and cross-functional collaboration skills
Commitment to quality and compliance excellence

Responsibilities

Inspect incoming materials to confirm compliance with purchase order specifications.
Audit in-process components, sub-assemblies, and finished products to verify conformance to specifications.
Perform First Article Inspections and prepare associated reports.
Conduct lot release testing with support from engineering or senior quality personnel.
Maintain identification and traceability of materials during inspection activities.
Follow Quality System requirements and all applicable SOPs in the Training Matrix.
Accurately complete Lot History Records (LHRs) and inspection documentation.
Maintain documentation in accordance with Quality Manual and work instructions.
Perform line clearance audits to support compliant production operations.
Prepare inspection stations, ensuring organization and cleanliness.
Identify defects and nonconformances and communicate findings to supervisors, engineers, and production leadership.
Maintain reject logs and document inspection results accurately.
Inform supervisors of equipment issues or needed tool repairs.
Demonstrate defect awareness and understanding of impact to product quality.
Maintain strong working relationships with peers and cross-functional teams.
Support production quality initiatives and continuous improvement efforts.
Work overtime as needed to support production demands.
Perform additional duties as assigned.