Manufacturing Engineer III
- Wheeling, IL, United States
Applications open in a new tab.
Job details
- Posting language
- English
- Posted
Original job description
Focus-Driven:
- Automation experience
- Swiss Machining
- Advanced manufacturing process (CNC machining, injection molding, stamping)
- PLC, a plus
We offer market competitive compensation. Potential salary range for this role is $90k-$120k. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.
Benefits:
- New employees are eligible for the following benefits effective date of hire!
- Medical, dental, and vision benefits
- Company-paid life insurance and disability benefits
- Generous Paid time off and 10 paid Holidays
- 401k Plan with Company Match
- Tuition Reimbursement
- Voluntary Universal Life and Long-Term Care
- Voluntary Legal Plan
- Pet Insurance
- Home Ownership Program
Why Join Us?
Looking for work that matters? Join Viant and contribute to the design and manufacturing of medical technologies that improve patient outcomes. Guided by our promise - We’re In It For Life - you’ll build your career with a trusted industry innovator that invests in your growth, well-being, and ability to make a meaningful impact every day.
About the Company
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With nearly 6,000 employees across 24 locations worldwide, we help bring innovative healthcare technologies to market efficiently and reliably.
About the Site
Located in Wheeling, IL our facility focuses on precision machining of metal components, supporting high-performance medical device manufacturing.
About the Role
As a Manufacturing Engineer, you will be responsible for improving manufacturing processes, supporting production operations, and ensuring products are produced safely, efficiently, and in compliance with quality and regulatory requirements. This role serves as a key link between engineering, production, quality, and suppliers to drive continuous improvement and operational excellence.
Job Responsibilities:
- Follow all manufacturing Good Manufacturing Practices (GMP’s) as defined by Viant Medical’s practices, policies and Standard Operating Procedures (SOP’s)
- Performs project management responsibilities for assigned manufacturing changes or new product methods, designs of production fixtures, and methods to monitor efficiency
- Evaluates existing machinery and processes to recommend improvements that enhance both operator performance and ergonomics/safety of overall production
- Optimizes floor layout, material flow, along with implementation of lean concepts; document improvements to manufacturing efficiencies, takt time, floor space utilization and overhead.
- Develops or revises technical documentation to specify manufacturing processes; including documentation of equipment qualification, setup and maintenance procedure
- Conducts research and development testing and validation to determine effectiveness and compliance to quality standards for the manufacturing processes
- Confirms conformance to engineering designs and methodologies and verify overall safety and prepares reports on these activities
- Confers with vendors to determine product specifications and arrange for purchase of equipment, materials, or parts, and evaluates products according to specifications and quality standards
- Utilizes proven lean manufacturing based analytical and troubleshooting/problem solving abilities to identify opportunities for cost reduction, lead-time reduction, inventory reduction and quality improvement through defect reduction
- Performs other duties as needed
Education/Experience
- Minimum 3 years of experience in the medical device industry or another regulated manufacturing environment.
- Minimum 2 years of experience supporting new product development and quality engineering activities.
- Experience with metal processing
- Minimum 2 years programming & hands on problem solving knowledge of machining
- Bachelor's degree in Engineering, Quality, Manufacturing, or a related technical or scientific field, or equivalent combination of certification and experience. CQE certification is a plus.
- Experience with FDA regulations, ISO 13485, and quality management systems preferred.
Competencies
- Strong knowledge of quality engineering principles, including SPC, FMEA, DOE, process validation, root cause analysis, and CAPA methodologies.
- Proficient in statistical analysis, Microsoft Excel, Minitab, and measurement system evaluation techniques.
- Skilled in supplier quality management, qualification processes, audits, corrective actions, and continuous improvement initiatives.
- Working knowledge of Lean Manufacturing and Six Sigma methodologies.
- Strong analytical, troubleshooting, and problem-solving capabilities.
- Excellent verbal and written communication skills with the ability to deliver training and collaborate across cross-functional teams.
- Effective project and priority management skills with the ability to work independently in fast-paced manufacturing environments.
Benefits (effective Day 1)
- Medical, dental, and vision coverage
- 401(k) plan with company match
- Generous paid time off and paid holidays
- Low-cost nutrition and mental health visits
- Tuition reimbursement and career development programs
- Company-paid life insurance
- Access to individualized financial planning
- Employee discount programs
- Home ownership program
Compensation
We offer market competitive compensation. Potential salary range for this role is $95,000 - $120,000 annually. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.
Apply Today
Ready to build a rewarding career while helping improve patient lives around the world? Join a team that values innovation, collaboration, and continuous growth. We look forward to learning how your talents can contribute to Viant's mission.
Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life-enhancing medical devices. We do this through our depth and breadth of capabilities, end-to-end integration, technical expertise, and relentless focus on our customers and on operational excellence. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. For more information, visit viantmedical.com or follow us on LinkedIn. Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.
More about this job
Skills
- Machining
- Apply advanced manufacturing
- CNC machining
- PLC
- Manufacturing processes
- Regulatory compliance
- Process improvement
- Good manufacturing practices
- Project management
- Ergonomics
- Documentation
- Research
- Lean manufacturing
- Troubleshooting
- Problem solving
- Quality assurance procedures
- Engineering principles
- SPC
- Root cause analysis
- Statistics
- Microsoft Excel
- Minitab
- Communication skills
- Provide training
- Work independently