Engineering Manager, NPI

Viant Medical Inc.; Wheeling (IL); On-site; USD 135,000 - 150,000; Full time

Benefits offered by this job

Medical, dental & vision benefits

Company-paid life insurance & long‑/短期

Generous PTO & 10 holidays

401k with company match

Tuition reimbursement

Voluntary life & long-term care

Voluntary legal plan

Pet insurance

Home ownership program

Job summary

Viant Medical Inc. in Wheeling, IL, seeks an NPI Engineering Manager to lead the engineering team through new product introduction, industrialization, and process development for metal-centric medical device products.

You will partner with customers, Operations, Quality, Manufacturing and Supply Chain to transfer products from concept to production, ensuring safety, quality, delivery, and cost objectives while supporting growth.

Qualifications

• Bachelor of Science in Engineering or related discipline; advanced degree preferred.
• 7+ years engineering experience in regulated manufacturing (medical devices preferred).
• 4+ years of leadership experience incl. managing teams and cross-functional programs.
• Experience leading NPI, product industrialization, process development, design transfer, validation, and commercialization.
• Experience with metal-centric manufacturing processes and precision production.
• Working knowledge of FDA, ISO, OSHA, and quality-system requirements.
• Strong leadership, communication, and project-management skills in cross-functional environments.
• Understanding of design transfer, manufacturing process development, and validation within regulatory QMS.
• Knowledge of FDA and ISO requirements for medical devices.
• Track record of problem solving, risk reduction, and product launches.
• Experience with DOE, capability analysis, statistics (t-tests, ANOVA).
• Proficiency with engineering documentation (IQ/OQ/PQ, protocols, SOPs, reports).
• Advanced proficiency in Microsoft Office, Excel, and Minitab.
• Lean Six Sigma Green Belt preferred; Black Belt a plus.

Responsibilities

• Lead NPI activities from concept through commercialization and handoff to Operations.
• Manage engineering resources, priorities, timelines, and budgets for customer programs and manufacturing readiness.
• Collaborate with customers and internal teams on DFM, DFA, technical reviews, risk assessments, and design transfer.
• Develop and implement robust manufacturing processes for metal-centric components and assemblies.
• Drive process characterization, DOE, equipment qualification, and validation activities (IQ/OQ/PQ).
• Lead cross-functional teams to execute product launches within safety, quality, delivery, and cost targets.
• Create manufacturing readiness plans covering equipment, tooling, fixtures, and capacity.
• Evaluate new technologies, automation, and tooling to meet product needs and growth.

Skills

People leadership

Project management

Communication

Cross-functional collaboration

Problem solving

Lean Six Sigma

Quality system knowledge

Education

Bachelor's degree in Engineering

Advanced degree preferred

Tools

Microsoft Office

Excel

Minitab

Job description

Posted Tuesday, August 4, 2026 at 5:00 AM

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, it delivers high-quality, life-enhancing products with the scale and expertise to bring devices to market efficiently. Learn more at Viant Medical’s website or on LinkedIn.

About the site:

Our Wheeling facility combines precision machining and assembly capabilities to deliver high-quality medical device components and finished products.

About the role:

The NPI Engineering Manager will lead and develop the Engineering team with primary responsibility for New Product Introduction (NPI), product industrialization, and process development. This role is accountable for successfully transferring new products from concept and design into production by establishing robust manufacturing processes, validation strategies, and scalable production systems. The NPI Engineering Manager will partner closely with customers, Operations, Quality, Manufacturing, and Supply Chain to ensure new products meet safety, quality, delivery, and cost objectives while supporting long-term business growth. This role will primarily support metal-centric medical device products and manufacturing processes. Additionally, this leader will collaborate with the site leadership team to grow partnerships with new and existing customers by promoting a culture of consistently meeting or exceeding customer expectations through Continuous Improvement, Operational Excellence, and High-Performance Teams.

We offer market competitive compensation. Potential salary range for this role is $135k-$150k. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.

Benefits: Eligible for 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

What you'll do:

• Lead NPI activities from concept through commercialization, production launch, and stable handoff to Operations.
• Manage engineering resources, project priorities, timelines, and budgets to support customer development programs, business growth initiatives, and manufacturing readinessobjectives.
• Partner directly with customers and internal teams on Design for Manufacturability (DFM), Design for Assembly (DFA), technical reviews, risk assessments, quoting support, and design transfer activities.
• Develop and implement robust manufacturing processes for medical device components and assemblies, with emphasis on metal-centric technologies such as CNC machining, Swiss turning, precision grinding, laser processing, metal forming, finishing, and secondary operations.
• Drive process characterization, Design of Experiments, equipment qualification, process development, and validation activities, including IQ, OQ, PQ, and controlled Engineering Studies when supported by approved rationale.
• Lead cross-functional teams to execute product launches within established safety, quality, delivery, cost, and budget expectations.
• Develop manufacturing readiness plans addressing equipment, tooling, fixtures, gauges, inspection methods, work instructions, capacity, staffing, supply chain, and production controls.
• Evaluate and implement new manufacturing technologies, automation solutions, capital equipment, andtoolingto support product requirements and future business growth.
• Ensure NPI activitiescomply withViant Quality System requirements, FDA regulations, ISO standards, customer requirements, and EHS policies.
• Apply lean manufacturing, risk management, and project management methodologies to improve engineering execution and accelerate commercialization timelines.
• Translate customer and product requirements into scalable manufacturing solutions that deliver capable processes, quality performance, and operational efficiency.
• Promote accountability, innovation, collaboration, and continuous learning within the engineering team.
• Support team development through coaching, performance reviews, succession planning, and alignment with Viant values and career growth opportunities

Requirements

Education/Certification/Experience:

• Bachelorof science degreeinEngineeringor related discipline, advanced degreepreferred
• 7+years of engineering experience in a regulated manufacturing environment, preferably within the medical device industry.
• 4+ years ofdemonstratedpeopleleadership, technical leadership, or project leadership, including responsibility for engineering teams and cross-functional programs.
• Demonstrated experience leading NPI, product industrialization, process development, design transfer, validation, and commercialization projects.
• Experience with metal-centric manufacturing processes and precisioncomponentproductionstronglypreferred.
• Working knowledge of FDA, ISO, OSHA, and applicable quality-system requirements.
• Strong leader, clear communicator, and highly organized project manager with the ability to manage multiple customer programs and competing priorities.
• Excellent interpersonal, conflict-resolution,team-building, and influencing skills across technical, operational, and customer-facing environments.
• Strong understanding of design transfer, manufacturing process development, process validation, product commercialization, and production ramp-up within a regulated Quality ManagementSystem..
• Strong understanding of FDA and ISO requirements applicable to medical device development and manufacturing.
• Demonstratedtrack recordof creative problem solving, risk reduction, and successful product launches.
• Direct experience with process characterization, Design of Experiments, capability analysis, and statistical methods, including t-tests, ANOVA, and significance testing.
• Expertisein technical documentation, including engineering reports, risk assessments, protocols, IQ/OQ/PQ documentation, Engineering Studies, SOPs, and work instructions.
• Advancedproficiencywith Microsoft Office, Excel, and Minitab.
• Lean Six Sigma Green Belt preferred; Black Belt certification is a plus.

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.