Top 7 Quality engineer medical device Jobs in Rockford, Il

Manufacturing Process Engineer
Katalyst Healthcares & Life Sciences —Rockford, IL
- Contract
- Hybrid work
- 5 years
- Mid-level
- Communication skills
Quick Apply
Project engineer lll
PCI Pharma Services —Rockford, IL
- $97,280 - $109,440 a year
- Full-time
- Mentoring
- Budgeting
- In-person
- Health insurance
- Dental insurance
Quick Apply
1d
Sr. Manager, Quality Engineering ADD
PCI Pharma Services —Rockford, IL
- $108,690 - $136,200 a year
- Full-time
- 5 years
- Computer literacy
- Engineering
- AD&D insurance
- Health insurance
Manager, Facilities & Software Validations
PCI Pharma Services —Rockford, IL
- $108,960 - $122,580 a year
- Overtime
- 6 years
- Computer Science
- Computer literacy
- Health insurance
- Dental insurance
Project Engineer III
PCI Pharma Services —Rockford, IL
- $97,280 - $109,440 a year
- Full-time
- Mentoring
- Budgeting
- Senior level
- Health insurance
- Dental insurance
Validation Engineer
Haumiller Engineering Co —Belvidere, IL
- $73,000 - $95,000 a year
- Full-time
- Mid-level
- 3 years
- Travel
- Health savings account
- AD&D insurance
Quick Apply
1d
Process Engineer
Fives Landis Corp. —Rockford, IL
- $70,000 - $90,000 a year
- Full-time
- Mid-level
- Analysis skills
- Computer skills
- Paid holidays
- Health insurance
Quick Apply

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quality engineer medical device jobs near rockford, il

Manufacturing Process Engineer

Katalyst Healthcares & Life Sciences -
Rockford, IL

Quick Apply

Job Details

Contract

Qualifications

Defect resolution root cause analysis
Technical documentation
Six Sigma methodology implementation
Factory operations documentation
Manufacturing facility experience
Bachelor's degree in engineering
Production validation processes
Productivity software
Commissioning phase involvement
Quality improvement programs in engineering
Implementing lean manufacturing processes
Failure analysis

Full Job Description

Job Description:
We are seeking a Manufacturing Process Engineer to support manufacturing operations by developing, optimizing, and validating production processes to improve efficiency, quality, and productivity. The ideal candidate will work closely with Manufacturing, Quality, Operations, R&D, and Supply Chain teams to drive continuous improvement initiatives, resolve production issues, and ensure compliance with safety and regulatory requirements in a fast-paced manufacturing environment.
Roles & Responsibilities:

Develop, implement, and optimize manufacturing processes to improve productivity, quality, and cost efficiency.
Analyze manufacturing workflows and identify opportunities for process improvements using Lean Manufacturing and Six Sigma methodologies.
Support new product introduction (NPI), process development, and technology transfer activities.
Design, validate, and document manufacturing processes, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), where applicable.
Investigate production issues, perform root cause analysis, and implement corrective and preventive actions (CAPA).
Create and maintain process documentation, work instructions, Standard Operating Procedures (SOPs), and manufacturing specifications.
Collaborate with cross-functional teams including Manufacturing, Quality Assurance, R&D, Maintenance, Supply Chain, and Regulatory Affairs.
Support equipment selection, installation, commissioning, and validation activities.
Monitor process performance using statistical tools such as Statistical Process Control (SPC) and process capability analysis.
Lead continuous improvement initiatives focused on cycle time reduction, waste elimination, yield improvement, and cost savings.
Participate in Failure Mode and Effects Analysis (FMEA), risk assessments, and process validation activities.
Support manufacturing scale-up, process transfers, and production line improvements.
Ensure compliance with company quality systems, safety procedures, and applicable regulatory requirements including GMP/cGMP, FDA, and ISO standards.
Train manufacturing personnel on new processes, equipment, and standardized work procedures.
Prepare technical reports, engineering documentation, and project status updates.

Requirements:

Bachelor's degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, Chemical Engineering, Biomedical Engineering, or a related engineering discipline.
2 5 years of manufacturing or process engineering experience.
Experience supporting manufacturing operations in regulated or high-volume production environments.
Knowledge of Lean Manufacturing, Six Sigma, and Continuous Improvement methodologies.
Experience with process validation, root cause analysis, and problem-solving techniques.
Strong understanding of manufacturing documentation and engineering change processes.
Excellent analytical, organizational, and communication skills.
Proficiency with Microsoft Office Suite.

Preferred Qualifications:

Experience in Medical Device, Pharmaceutical, Biotechnology, Automotive, Aerospace, or Electronics manufacturing.
Knowledge of GMP/cGMP, FDA regulations, ISO 13485, ISO 9001, or AS9100.
Experience with CAD software (SolidWorks, AutoCAD, Creo, or equivalent).
Familiarity with ERP and Manufacturing Execution Systems (MES).
Green Belt or Black Belt certification in Lean Six Sigma.
Experience with automation, robotics, PLCs, or manufacturing equipment integration.

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Refine Your Search

quality engineer medical device jobs in rockford, il

Manufacturing Process Engineer

Project engineer lll

Sr. Manager, Quality Engineering ADD

Manager, Facilities & Software Validations

Project Engineer III

Validation Engineer

Process Engineer

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