Production Engineering Associate
Medical Murray
Summary
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.
Job description
Why You’ll Love This Role
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.
What You’ll Do
Support Daily Production Operations
- 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.
Strengthen Documentation & Quality Systems
- 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.
Maintain Label, Material & Equipment Control
- 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.
Drive Continuous Improvement & Compliance
- 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.
What You’ll Bring
Education
- 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
Experience
- 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.
Technical & Professional Skills
- 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.
Requirements
- High School Diploma or GED required
- Associate degree in Business Administration, Manufacturing, Engineering Technology, or related field preferred
- 2–4 years of experience in a manufacturing, production, or operations support role
- 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
Benefits
- Medical, Dental & Vision
- Company-paid life insurance
- Short-term disability
- Long-term disability
- HSA-eligible plans
- 401(k) Safe Harbor
- 18 days PTO
- TeleDoc access
- Identity protection
- Tuition reimbursement
- Voluntary life insurance
- Community volunteering PTO
Company overview
Medical Murray is a privately-owned contract development and manufacturing organization (CDMO) specializing in the design, development, and production of complex medical devices for minimally invasive procedures. Founded in 1996 and headquartered in North Barrington, Illinois, the company has established itself as a leading provider of innovative catheter systems, permanent implants, and bioabsorbable devices for vascular, urology, and surgical applications. With ISO 13485:2016 certification and FDA-registered facilities across multiple locations in Illinois and North Carolina, Medical Murray offers comprehensive services ranging from initial concept development and prototyping to full-scale manufacturing, assembly, packaging, and sterilization. The company's expertise includes complex catheter systems, delivery systems, steerable devices, balloon catheters, covered stents, and advanced material technologies including nitinol, ePTFE, and bioabsorbable polymers. Serving clients from startups to large OEMs, Medical Murray operates Class 7 certified cleanrooms and maintains an ISO/IEC 17025:2017 accredited testing laboratory for rigorous device validation. The company's collaborative approach and technical proficiency have made it a trusted partner in bringing innovative medical devices to market across cardiovascular, neurovascular, orthopedic, gastroenterology, and urology markets.