Design Developer Jobs in Niagara Falls, NY (NOW HIRING)

Company

Simplifying Oxygen, Nitrogen, Medical Air and Vacuum

ABOUT NOVAIR

Novair USA Corp is a diversified manufacturing company with its headquarters and production facility located in North Tonawanda, NY USA. Novair USA operates as a fully owned subsidiary of Novair Groupe, a global leader in the manufacturing of oxygen and nitrogen generating systems for industrial and medical applications.

NOVAIR USA’s Mission

Novair USA Corp is committed to profitably producing quality products and attaining a high level of customer satisfaction. To achieve this, we are honest, we treat each other respectfully, we are open to change, and we strive to continuously improve.

Job Description

Position Title: Design Engineer

City Based: North Tonawanda, NY1

Job Summary

Duties include but are not limited to:

This is a hands-on Design Engineer role requiring a Mechanical, Biomedical, Aerospace, or Electrical Engineering degree with a solid design engineering background, preferably within medical gas systems, industrial gas generation, or a related manufacturing industry. The Design Engineer serves as a key liaison between customers, vendors, sales, and the manufacturing floor.

1. Design Engineer Core Responsibilities

Priority is placed on design ownership, product development, and engineering excellence:

• Design new product lines, redesign legacy products or develop complete custom systems for customers based on specifications provided by the sales team. Create complete drawing packages including 3D models, detailed drawings, schematics, P&IDs, and Bills of Material.

• Create, correct, and revise part drawings, assemblies, subassemblies, and top-level product drawings using 3D CAD (SolidWorks preferred).

• Lead and participate in hands-on R&D projects for new product development, product improvement, cost reduction, and new product implementation.

• Participate in the creation of Design History Files (DHF) for product lines in preparation for FDA 510(k) submissions for medical devices when applicable — including identification of user needs, design inputs/outputs, design verification/validation, risk assessment, and design traceability matrices.

• Drive continuous improvement of company productivity and efficiency by reducing total production costs through improved design, Design for Manufacturing (DFM), ease of fabrication, and qualification of alternative vendors/components.

• Source, test, and implement new componentry as part of cost-savings and performance-improvement initiatives.

• Attend and participate in Job Feasibility and Contract Review meetings. Review job specifications and provide engineering sign-off for approval or rejection of contracts.

• Provide Engineering Change Notice (ECN) and Temporary Deviation authority and approval.

2. General Engineering & Sustaining Support Responsibilities

• Maintain and update Bills of Material (BOM) on drawings — verify correct parts, quantities, and part numbers; ensure Master BOM owners are notified of changes.

• Read and interpret blueprints, technical drawings, schematics, P&IDs, specifications, scope of supply contracts, and customer-generated reports.

• Utilize the Engineering Change Notice (ECN) system and Product Data Management (PDM) software to ensure only current and correct drawing versions are used.

• Follow ISO Design Procedures (ISO 9001 / ISO 13485) and contribute ideas for continuous improvement of those procedures.

• Direct and assist in the assembly of product manuals and improve the manual creation process.

• Monitor and review drawing packages, engineering documentation, and procedures; intervene to prevent release of inaccurate documentation.

   The role involves standard design, test, and product-improvement engineering duties together with product support and Design for Manufacturing responsibilities.

Work Experience / Qualifications

The ideal candidate will have 5+ years of hands-on design engineering experience (3–5+ years minimum considered for strong candidates) in:

• Demonstrated ability to design products from concept through production release and to improve existing product designs.

• 3D modeling — SolidWorks strongly preferred; fluency in professional 3D CAD software required.

• 2D CAD for schematic generation (AutoCAD or equivalent).

• Implementing lean / Six Sigma concepts is a plus.

• Knowledge of programming and operating 3D and resin printers is a plus (used for R&D projects).

• Background in ISO 9001, ISO 13485, FDA 510(k), and/or medical devices is highly preferred but not limiting.

Additional required attributes:

• Superior organizational skills, accuracy, and attention to detail.

• Strong project management and multi-tasking ability; manages time effectively and adapts to a fast paced environment.

• Effective listening, verbal, and written communication skills.

• Team player who works productively with a wide range of people.

• Demonstrated integrity and ethical standards.

• Proficiency with Microsoft Office Suite, use of AI tools for enhancing productivity and some familiarization with SAP or other ERP system.

Note: Entry-level engineering candidates are not eligible for this Design Engineer role.

Soft Skills

Ability to multi-task and meet deadlines. Strong communication and teamwork skills. Relationship builder. Problem solver. Ability to work with a diverse group. Positive attitude. Works well independently. Follows policies and procedures. Embraces new ideas and change. Follows core values: mutual trust and respect for all, consistency of purpose and process, ethical in everything we do, and customer focus.

How Success is Measured

Success will be measured by specific quantitative goals, including but not limited to:

• % On-time delivery of engineering documents (actual vs. committed date), hitting project milestones on time and on budget

• % Reduction in production costs (COGS for similar models) year over year if project goal specifies this metric

• % Reduction in engineering time to produce floor-ready packages

• Quality and completeness of Design History Files and drawing packages released

Work Environment

Environment

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Physical Demands

While performing the duties of this job, the employee is regularly required to sit, talk, and listen. The employee is occasionally required to stand and walk on a production floor. The employee must occasionally lift and/or move up to 10 pounds or more. Specific vision abilities required by this job include close vision and ability to adjust focus. Overall level of physical activity is light.

Equipment Used

Computer, keyboard, scanner, phone, copier, basic hand tools in R&D lab, 3D printer, resin printer, prototype mill and fabrication equipment where applicable

Education

• Bachelor’s degree or higher in Mechanical, Biomedical, Aerospace, or Electrical Engineering required.

• 5+ years in a similar design engineering position preferred; strong 3–5 year candidates will be considered. Must have existing engineering job experience.

Compensation

TBD — competitive for mid- to senior-level design engineering talent

Benefits / Medical

See Attachment

Revised

08-07-2026

Hiring Manager

Loyd Weldy

Website to Apply

www.novair-usa.com

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. The above statements are not meant to be all inclusive. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.

Department / Reports to

Engineering Manager