Product Manager

Medical Murray • Lake Zurich, IL

6h

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.

If you are detail-oriented, analytically minded, and thrive in structured manufacturing environments where quality and compliance matter, this role offers meaningful impact.

As a Production Engineering Associate, you will be a key operational partner to Production, Engineering, and Quality — ensuring documentation accuracy, supporting material flow, reinforcing cleanroom readiness, and driving continuous improvement initiatives. Your work directly supports compliant production execution and protects product integrity in a regulated manufacturing environment.

This is an excellent opportunity for someone who enjoys connecting data, documentation, and process execution to improve performance and ensure operational excellence.

Requirements

• High School Diploma or GED required
• Associate degree in Business Administration, Manufacturing, Engineering Technology, or related field preferred
• Equivalent combination of education and relevant experience considered
• 2–4 years of experience in a manufacturing, production, or operations support role (regulated environment preferred).
• Experience supporting production documentation such as NCRs, CAPAs, and Lot History Records preferred.
• Experience in cleanroom, assembly, or controlled manufacturing environments preferred.
• Familiarity with ERP systems and electronic documentation systems preferred.
• Experience collaborating cross-functionally with Production, Quality, and Engineering teams.
• Strong proficiency in Microsoft Office and general computer systems.
• Excellent attention to detail with strong analytical and problem-solving skills.
• Ability to interpret manufacturing and quality data to support decision-making.
• Strong organizational skills with the ability to manage multiple priorities.
• Clear written and verbal communication skills.
• Ability to follow SOPs and work effectively within a quality management system.
• Familiarity with lean manufacturing principles is a plus.

Nice To Haves

• Familiarity with project management
• Familiarity with Customer Service
• Familiarity with Manufacturing Medical Devices

Responsibilities

• Monitor material availability and proactively communicate shortages to Production and Engineering teams.
• Provide material delivery support (water spider activities) to ensure timely component availability.
• Track and maintain employee training records within the learning management system.
• Review and validate production time entries and assist with job closures.
• Initiate, track, and manage Production-related Nonconformance Reports (NCRs), ensuring accurate documentation and timely follow-up prior to Quality submission.
• Execute and track Corrective and Preventive Action (CAPA) activities to closure.
• Perform Lot History Record (LHR) reviews to confirm completeness and accuracy.
• Identify and segregate nonconforming products; escalate issues appropriately.
• Assist supervisors with training certifications and document revision alignment.
• Conduct training and retraining online clearance procedures.
• Serve as backup for line clearance verification as assigned.
• Scan, file, and maintain production documentation within SharePoint and controlled repositories.
• Enter, control, and report production data through ERP/MRP systems.
• Serve as a trained Label Receiver, ensuring proper issuance, traceability, reconciliation, and disposal of labels.
• Verify label accuracy prior to distribution to production.
• Assist with organization and verification of tooling, fixtures, and production equipment.
• Collect and compile KPI data including Quality, Safety, Attendance, Productivity, and Scrap metrics.
• Support visual management and best-practice implementation on the manufacturing floor.
• Participate in audits, investigations, root cause analyses, and improvement initiatives.
• Maintain oversight of Preventive Maintenance schedules and verify completion of required activities.
• Perform additional duties in support of manufacturing operations as needed.

Benefits

• We offer a competitive compensation and benefits package, including medical (BCBS) and dental coverage, company-paid vision and life insurance, short- and long-term disability, HSA-eligible plans, a 401(k) Safe Harbor retirement plan, 18 days of PTO, TeleDoc access, identity protection, tuition reimbursement, voluntary life insurance, and paid time off for community volunteering.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED