Envista

Global dental products & technologies provider

Mechanical Engineer 3

Design EngineeringConfirmed live in the last 24 hours

Full-timeQuakertown, PA, USA

About the Job

Requirements

A bachelor's degree in Mechanical Engineering or an equivalent technical discipline.
At least 10 years of relevant experience in mechanical product design, sustaining engineering, new product development, design transfer, manufacturing support, or a closely related engineering role; an advanced degree may be considered in combination with relevant experience.
Ability to independently complete complex engineering assignments with minimal guidance and make sound engineering recommendations based on data, analysis, risk, and business needs.
Strong working knowledge of mechanical parts, assemblies, mechanisms, materials, tolerancing, drawings, specifications, and design for manufacturability.
Proficiency with 3D CAD and 2D drawing tools such as SolidWorks, Creo, or equivalent; SolidWorks is preferred.
Hands-on experience with testing, prototyping, troubleshooting, root-cause analysis, and verification of mechanical designs, products, or fixtures.
Working knowledge of design control documentation, engineering change control, risk-based decision making, and cross-functional product development practices.
Ability to lead small to moderate technical workstreams, coordinate cross-functional input, mentor less-experienced team members, and influence without direct authority.
Proficiency with Microsoft Word, Excel, PowerPoint, and standard engineering documentation practices.

Responsibilities

Lead or support engineering projects from initial concept and project specification through design, prototype build, verification, design transfer, manufacturing implementation, and post-launch support.
Develop mechanical designs, assemblies, components, fixtures, tooling, and related specifications while balancing safety, reliability, manufacturability, serviceability, cost, and user needs.
Work with cross-functional teams to translate customer, regulatory, quality, manufacturing, and business requirements into practical mechanical design solutions.
Prepare and maintain engineering documentation for multiple audiences, including design inputs, design outputs, drawings, bills of material, test protocols, test reports, engineering analyses, engineering change notices, and design history file content as applicable.
Participate in and potentially lead cross-functional design reviews, failure mode and effects analysis activities, risk analysis, usability or human factors reviews, troubleshooting sessions, and technical decision reviews.
Develop verification strategies and write or review test protocols for mechanical products, components, assemblies, fixtures, and design changes.
Perform hands-on testing, prototyping, troubleshooting, root-cause analysis, and design iteration using engineering judgment and data from multiple sources.
Interpret legacy designs and perform sustaining engineering activities, including product support, component obsolescence resolution, supplier changes, value engineering, and continuous improvement.
Interface with manufacturing, subcontractors, suppliers, and international design teams during design transfer, technical support, and vendor coordination.
Design, fabricate, or coordinate test parts, equipment, jigs, and fixtures using internal resources, suppliers, basic machine tools, and rapid prototyping methods as appropriate.
Support Regulatory Affairs and Quality Assurance by integrating applicable design control, risk management, regulatory, and quality system requirements into engineering work.
Facilitate or contribute to the engineering change notice process for cross-functional workstreams and ensure assigned engineering deliverables are completed with appropriate quality, traceability, and timeliness.
Prioritize and manage multiple projects or activities with limited supervision, elevating risks, tradeoffs, and resource needs in a timely and professional manner.
Provide technical guidance, peer review, coaching, and support to engineers, co-ops, interns, and colleagues with less experience, without direct supervisory authority.
Demonstrate leadership behaviors including accountability, clear communication, collaboration, constructive feedback, and building consensus across functions.
Support continuous improvement and Envista Business System activities such as Daily Management, Problem Solving Process, Visual Project Management, and standard work improvement as applicable.
Complete other duties as assigned.
Model accountability by owning commitments, following through on deliverables, and communicating risks or decisions early.
Build trust with cross-functional partners by listening, clarifying requirements, and aligning technical recommendations with customer, quality, regulatory, operational, and business needs.
Provide informal guidance to less-experienced engineers and help raise the team's technical capability through mentoring, peer review, and practical coaching.
Use data, structured problem solving, and professional judgment to resolve complex issues and drive timely decisions.
Demonstrate readiness for future people leadership through consistency, composure, documentation discipline, prioritization, and influencing outcomes without formal authority.

Desired Qualifications

Experience in a regulated industry such as medical device, aerospace, or automotive.
Experience with design control, design for manufacturability, good manufacturing practices, the U.S. Food and Drug Administration, International Organization for Standardization 9001, International Organization for Standardization 13485, risk management, or related quality system requirements.
Experience supporting U.S. Food and Drug Administration 510(k)-cleared medical devices or regulated product submissions.
Intermediate to strong knowledge of materials properties and associated processing techniques, including plastic injection molding, computer numerical control machining, sheet metal forming or stamping, casting, and additive manufacturing.
Experience with failure mode and effects analysis, fault tree analysis, risk analysis, usability or human factors considerations, component selection, reliability principles, value engineering, and design for assembly.
Experience with basic machine shop equipment, 3D printing equipment, prototype fabrication, and fixture development.
Formal project management, technical leadership, Lean, Envista Business System, or continuous improvement training.
Demonstrated interest or capability in developing people, improving team effectiveness, and preparing for a future management or technical leadership role.

Job Description:

DEXIS is looking for individuals who work their best, help others, and commit to helping us improve our customer lives and celebrate the difference in others.

Who is DEXIS and why should you join the team??

We are the leading manufacturer and distributor of innovative dental imaging equipment, software, and solutions. We offer meaningful work through innovation, diverse opportunities, and career progression.

We also offer

Competitive Pay and Sign on Bonuses.
PTO, Sick Time and Paid Holidays.
Competitive leave policies including but not limited to Sick, Jury Duty, Bereavement, Personal, and Parental Leave Medical, Dental, and Vision Insurance Benefits effective DAY ONE!!!!
401K – company match starting DAY ONE!!!!
Community involvement opportunities & employee appreciation events.
Newly renovated, state of the art, climate-controlled facility.
Newly built 1200 sq fitness room.
Gourmet coffee, beverages, snacks, and lunches are available in our café.
Employee Lounge with pool table, shuffleboard and skeet ball for downtime and employee fun!

Where are we?

Situated on the southern edge of the Lehigh Valley and easily accessible from northern Philadelphia suburbs and the surrounding areas, the Quakertown facility is our North American hub for the design and manufacturing of leading dental imaging devices and software. The facility has a growing, energetic, and diverse mix of professionals spanning engineering, operations, regulatory and quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open atmosphere helps to foster strong personal and professional relationships across the organization.

Position Description

The Mechanical Engineer III is an experienced individual contributor responsible for supporting existing products through their product life cycle and leading or supporting the development of new mechanical products, subsystems, fixtures, and product improvements for domestic and global markets. The role works cross-functionally with Regulatory, Marketing, Quality, Operations, Manufacturing, Supply Chain, vendors, and other engineering disciplines to drive product changes, design control deliverables, sustaining engineering support, continuous improvement, and design transfer activities.

This position requires in-depth mechanical engineering knowledge and practical product development experience. The Mechanical Engineer III works independently with minimal guidance on complex assignments, applies best practices and knowledge of internal and external business issues to improve products and processes, and serves as a technical resource for colleagues with less experience. The role is intended for an engineer who candemonstrateownership, sound judgment, cross-functional influence, and leadership qualities that support future progression into a people-management or technical-leadership role.

Essential Duties and Responsibilities:

Leads orsupportsengineering projects frominitialconcept and project specification through design, prototype build, verification, design transfer, manufacturing implementation, and post-launch support.

Develops mechanical designs, assemblies, components, fixtures, tooling, and related specifications while balancing safety, reliability, manufacturability, serviceability, cost, and user needs.

Works collaboratively with cross-functional teams to translate customer, regulatory, quality, manufacturing, and business requirements into practical mechanical design solutions.

Prepares andmaintainsengineering documentation for multiple audiences, including design inputs, design outputs, drawings, bills of material, test protocols, test reports, engineering analyses, ECNs, and design history file content as applicable.

Participates in and may lead cross-functional design reviews, FMEA activities, risk analysis,usabilityor human factors reviews, troubleshooting sessions, and technical decision reviews.

Developsverification strategies and writes orreviewstest protocols for mechanical products, components, assemblies, fixtures, and design changes.

Performs hands-on testing, prototyping, troubleshooting, root-cause analysis, and design iteration using engineering judgment and data from multiple sources.

Interprets legacy designs and performs sustaining engineering activities, including product support,componentobsolescence resolution, supplier changes, value engineering, and continuous improvement.

Interfaces with manufacturing, subcontractors, suppliers, and international design teams in design transfer, technical support, and vendor coordination situations.

Designs, fabricates, or coordinates test parts, equipment, jigs, and fixtures using internal resources, suppliers, basic machine tools, and rapid prototyping methods asappropriate.

Supports Regulatory Affairs and Quality Assurance activities by integrating applicable design control, risk management, regulatory, and quality system requirements into engineering work.

Facilitates or contributes to the ECN process for cross-functional workstreams and ensures assigned engineering deliverables are completed withappropriate quality, traceability, and timeliness.

Prioritizes and manages multiple projects or activities with limited supervision, elevating risks, tradeoffs, and resource needs ina timelyand professional manner.

Acts as a resource for engineers, co-ops, interns, and colleagues with less experience byprovidingtechnical guidance, peer review, coaching, and support without direct supervisory authority.

Demonstrates leadership behaviors consistent with future management potential, including accountability, clear communication, collaboration, constructive feedback, and the ability to build consensus across functions.

Supports and contributes to continuous improvement and Envista Business System activities such as Daily Management, Problem Solving Process, Visual Project Management, and standard work improvement as applicable.

Completes other duties as assigned.

Leadership and Management Readiness Expectations:

Models accountability by owning commitments, following through on deliverables, and communicating risks or decisions early.
Builds trust with cross-functional partners by listening, clarifying requirements, and aligning technical recommendations with customer, quality, regulatory, operational, and business needs.
Provides informal guidance to less-experienced engineers and helps raise the technical capability of the team through mentoring, peer review, and practical coaching.
Uses data, structured problem solving, and professional judgment to resolve complex issues and drive timely decisions.
Demonstrates readiness for future people leadership by showing consistency, composure, documentation discipline, prioritization, and the ability to influence outcomes without formal authority.

Job Requirements:

Minimum Qualifications:

Bachelor’s degree in Mechanical Engineering or equivalent technical discipline.
10+ years of relevant experience in mechanical product design, sustaining engineering, new product development, design transfer, manufacturing support, or a closely related engineering role; an advanced degree may be considered in combination with relevant experience; experience in a regulated industry such as medical device, aerospace, or automotive is highly desired
Demonstrated ability to independently complete complex engineering assignments with minimal guidance and to make sound engineering recommendations based on data, analysis, risk, and business needs.
Strong working knowledge of mechanical parts, assemblies, mechanisms, materials, tolerancing, drawings, specifications, and design for manufacturability.
Proficiency with 3D CAD and 2D drawing tools such as SolidWorks preferred, Creo, or equivalent.
Hands-on experience with testing, prototyping, troubleshooting, root-cause analysis, and verification of mechanical designs, products, or fixtures.
Working knowledge of design control documentation, engineering change control, risk-based decision making, and cross-functional product development practices.
Demonstrated ability to lead small to moderate technical workstreams, coordinate cross-functional input, mentor less-experienced team members, and influence without direct authority.
Strong written, verbal, and interpersonal communication skills, including the ability to explain technical information clearly and build consensus in complex or sensitive situations.
Proficiency with Microsoft Word, Excel, PowerPoint, and standard engineering documentation practices.

Preferred Qualifications:

Experience in a regulated industry such as medical device, aerospace, or automotive.
Experience with Design Control, DFM, GMP, FDA, ISO 9001, ISO 13485, risk management, or related quality system requirements.
Experience supporting FDA 510(k) cleared medical devices or regulated product submissions.
Intermediate to strong knowledge of materials properties and associated processing techniques, including plastic injection molding, CNC machining, sheet metal forming or stamping, casting, and additive manufacturing.
Experience with FMEA, fault tree analysis, risk analysis, usability or human factors considerations, component selection, reliability principles, value engineering, and design for assembly.
Experience with basic machine shop equipment, 3D printing equipment, prototype fabrication, and fixture development.
Formal project management, technical leadership, Lean, EBS, or continuous improvement training.
Demonstrated interest or capability in developing people, improving team effectiveness, and preparing for a future management or technical leadership role.

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Target Market Salary Range:

Actual compensation packages take into account a wide range of factors that are unique to each candidate, including but not limited to geographic location; skill sets; relevant education and certifications; depth of experience; performance; and other business and organizational needs. The disclosed reasonable estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Envista, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. The total compensation package for this position may also include an annual performance bonus, medical/dental/vision benefits, 401K match, and/or other applicable compensation plans.

For Field Sales roles, the salary range listed reflects base pay only and does not include incentive pay opportunities under the applicable sales compensation plan

$115,000 - $130,000

Operating Company:

DEXIS

Envista and all Envista Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available at: http://www.dol.gov/ofccp/regs/ compliance/posters/pdf/eeopost.pdf.

Envista and its family of companies (Envista) will not accept unsolicited resumes from any source other than directly from a candidate. Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening. Envista will not pay a fee to any Agency that does not have such agreement and written approval in place.

About the Company

Envista

Global dental products & technologies provider

Envista provides a broad range of dental products and solutions to dental professionals, spanning implants, prosthetics, orthodontics, imaging, endodontics, restorative materials, and infection prevention. Its products work by serving dentists through a two-segment model: Specialty Products & Technologies (brands like Nobel Biocare, Ormco, Damon System, Spark) and Equipment & Consumables (brands like Kerr, DEXIS, Metrex) sold via direct sales and distributors to offices, clinics, hospitals, and labs, enabling end-to-end workflows from planning and imaging to treatment and infection control. Envista differentiates itself with a large, globally distributed portfolio and established brands that cover roughly 90% of a dentist’s clinical needs, supporting DSOs and independent practices alike. The company aims to be a leading independent global provider of dental products and digital dentistry tools, expanding geographic reach and integrated solutions for dental care.

Company size: 1,001-5,000
Company stage: IPO
Headquarters: Brea, CA
Founded: 2004

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