Vision Correction Device Design Engineer – Irvine, CA
Are you a creative engineer passionate about innovation in vision care technology? We are seeking a Vision Correction Device Design Engineer to join a cutting-edge medical device company in Irvine, CA. In this role, you will be instrumental in designing and developing advanced ophthalmic devices that enhance quality of life for millions. If you thrive in a high-impact R&D environment and want to shape the future of vision correction, this opportunity is for you.
Design the Future of Vision Correction in Irvine, CA
A leading medical device company in Irvine, CA is looking for a Vision Correction Device Design Engineer to drive the development of next-generation vision correction technologies. The ideal candidate will bring a strong background in biomedical or mechanical engineering, proficiency in CAD tools, and a passion for improving patient outcomes. Join a mission-driven team dedicated to pushing the boundaries of what’s possible in ocular health.
Key Responsibilities of the Vision Correction Device Design Engineer – Medical Technology
Product Design & Innovation:
Design and develop advanced vision correction devices, including contact lenses, implantable devices, or wearable technologies. Leverage mechanical, biomedical, and optical engineering principles to create safe, effective, and innovative solutions aligned with user needs and industry trends.
Cross-Functional Collaboration:
Work closely with cross-functional teams including R&D, clinical, regulatory, and manufacturing to bring concepts from ideation to commercialization. Participate in design reviews, risk assessments, and usability evaluations to ensure product excellence and compliance.
Prototyping & Testing:
Create detailed 3D models, engineering drawings, and physical prototypes using CAD software and rapid prototyping tools. Design and execute experiments, analyze data, and iterate designs based on testing outcomes, customer feedback, and regulatory standards.
Regulatory & Quality Compliance:
Ensure all designs meet FDA, ISO, and other relevant medical device regulations and standards. Maintain thorough documentation throughout the product development lifecycle and contribute to design history files (DHF), technical files, and risk management reports.
User-Centric Engineering:
Apply human factors engineering and ergonomics to ensure optimal usability, comfort, and safety of vision correction devices. Integrate feedback from clinical studies, eye care professionals, and patients to refine designs and enhance the user experience.
Project Management:
Manage timelines, deliverables, and resource planning for assigned projects. Provide regular updates to leadership and stakeholders, identify risks, and proactively address design or development challenges to ensure timely project execution.
Material & Process Selection:
Research and select suitable biocompatible materials, manufacturing processes, and surface treatments that align with device requirements and cost targets. Collaborate with suppliers and manufacturing partners to scale production efficiently.
Continuous Improvement:
Stay current on emerging technologies, trends in ophthalmic devices, and advancements in material science. Contribute to innovation pipelines, process improvements, and knowledge sharing across engineering teams.
Intellectual Property Contribution:
Support patent development by contributing to invention disclosures and collaborating with legal teams. Protect innovative designs and ensure freedom to operate through careful analysis of existing IP landscapes.
Clinical Support & Post-Market Feedback:
Participate in clinical trial support and post-market surveillance by analyzing device performance, addressing field issues, and implementing design improvements for future iterations.
What the Client is Looking for in You
As a Vision Correction Device Design Engineer, the client is seeking a highly skilled and innovative professional with a passion for improving vision health through advanced medical technology. You should bring a strong technical background, a user-focused mindset, and the ability to thrive in a collaborative, fast-paced product development environment.
Expertise in Medical Device Design
The client is looking for an engineer with hands-on experience in the design and development of medical or vision-related devices. Proficiency in CAD tools, knowledge of materials used in ophthalmic products, and familiarity with device lifecycle development are essential. Experience in prototyping, testing, and refining high-precision components will set you apart.
Problem Solver with Innovative Thinking
You should be a creative problem solver who can balance innovation with practical design constraints. The ideal candidate can translate complex clinical requirements into functional and manufacturable device designs. The client values engineers who think critically, iterate efficiently, and drive continuous improvement.
Strong Understanding of Regulatory Standards
A solid grasp of FDA, ISO 13485, and other relevant regulatory standards is crucial for this role. The client is seeking someone who is detail-oriented and comfortable working in a highly regulated environment, with experience in maintaining compliant documentation and supporting submissions for product approvals.
Collaborative and Cross-Functional Communicator
Success in this role requires strong communication skills and the ability to work effectively across multidisciplinary teams. The ideal candidate will have experience collaborating with R&D, quality, regulatory, and manufacturing groups, and can contribute to shared project goals with clarity and accountability.
Passion for Improving Patient Outcomes
The client values individuals who are deeply motivated by the impact of their work. A strong interest in the medical technology field—particularly in improving vision care—and a user-centered approach to design are key. You should have a desire to create devices that improve lives, with quality, safety, and patient comfort in mind.
Attention to Detail and Engineering Discipline
A meticulous and disciplined engineering mindset is essential. The ideal candidate demonstrates technical precision, structured problem-solving, and thorough documentation throughout all stages of development. You should consistently deliver high-quality work in a deadline-driven setting.
Adaptable and Eager to Learn
Finally, the client values engineers who are curious, self-motivated, and open to learning. Experience with emerging technologies in the vision care space or a desire to grow expertise in this domain is highly regarded. Your ability to stay current with new tools, materials, and best practices will be critical to long-term success in this role.
FAQs About the Role – Vision Correction Device Design Engineer – Irvine, CA
1. What are the key responsibilities of the Vision Correction Device Design Engineer?
As a Vision Correction Device Design Engineer, your primary responsibilities include designing, prototyping, and refining vision correction devices that meet clinical requirements and user needs. You’ll collaborate with cross-functional teams in R&D, regulatory, quality, and manufacturing, while ensuring all product designs comply with industry standards and regulatory guidelines. You will also support product testing, documentation, and continuous design improvements throughout the device lifecycle.
2. What qualifications and experience are required for this position?
The ideal candidate will have a degree in Mechanical Engineering, Biomedical Engineering, or a related field, with hands-on experience in medical device design—preferably in ophthalmology or related areas. Proficiency in CAD software, familiarity with design for manufacturing (DFM), and a working knowledge of FDA and ISO standards are essential. Experience with prototyping, clinical validation, and regulatory documentation is highly preferred.
3. What skills are essential for success in this role?
Strong technical design capabilities, attention to detail, and analytical problem-solving skills are vital. You should be adept at translating clinical and user requirements into manufacturable device designs. Effective communication and collaboration skills are also important, as you will work closely with multidisciplinary teams to bring products from concept to market.
4. What challenges can I expect in this role?
You may face challenges related to balancing innovative design with regulatory constraints, meeting tight development timelines, and ensuring consistent product quality. Designing for small-scale precision, user safety, and comfort—while staying compliant with regulatory standards—will require a thoughtful and iterative approach. Navigating cross-functional input and evolving user needs can also be part of the design process.
5. What is the expected impact of this role on product development?
As a Design Engineer, your work will have a direct impact on the functionality, safety, and effectiveness of vision correction devices. Your contributions will support the development of next-generation ophthalmic solutions that improve patient outcomes and expand the company’s presence in the eye care market. This is a key role in delivering innovative, patient-centric products.
6. What is the work environment and company culture like?
The company offers a collaborative, fast-paced, and innovation-focused environment where engineers are encouraged to take initiative and contribute to meaningful healthcare solutions. The team values technical excellence, continuous learning, and a mission-driven approach to improving lives through vision technology.
What Remuneration Can You Expect from This Job?
As a Vision Correction Device Design Engineer based in Irvine, CA, you can expect a competitive compensation package that reflects your technical expertise, experience in medical device development, and your contribution to innovation in the field of vision correction. The remuneration typically includes the following components:
1. Base Salary
The average base salary for a Design Engineer in the medical device industry in Irvine ranges from $85,000 to $130,000 annually, depending on qualifications, years of experience, and the complexity of the role. Senior-level engineers or those with specialized ophthalmic device experience may command salaries toward the higher end of this range.
2. Performance-Based Bonuses
Many companies offer annual bonuses tied to performance metrics such as project milestones, product launch success, innovation achievements, and cross-functional collaboration. Bonuses typically range from 5% to 15% of the base salary.
3. Equity or Stock Options
If you’re joining a startup or a high-growth medical device company, you may be offered stock options or equity grants. These long-term incentives align your success with that of the company and can become a significant part of your total compensation as the company scales or reaches key funding or exit milestones.
4. Benefits Package
Employees typically receive a comprehensive benefits package that includes:
Health, dental, and vision insurance
401(k) retirement plans with employer match
Paid time off (PTO), sick leave, and holidays
Life and disability insurance
Employee wellness programs
Educational or professional development assistance
5. Relocation Assistance & Signing Bonus
For out-of-area candidates or high-value hires, companies may offer a signing bonus or relocation assistance to ease the transition. These one-time incentives can range from $5,000 to $20,000, depending on the company’s size and urgency to fill the role.
6. Career Growth & Non-Monetary Rewards
While financial compensation is competitive, this role also offers career advancement, exposure to cutting-edge ophthalmic technology, and the opportunity to work on products that improve lives. Recognition, autonomy, and participation in innovation-driven projects contribute to overall job satisfaction.
Total Compensation Potential
When you factor in salary, bonuses, equity, and benefits, the total annual compensation for this role can range from $95,000 to $160,000 or more, depending on experience, company performance, and the scale of responsibilities. In high-growth or VC-backed companies, equity could significantly increase long-term earning potential.
How to Apply
If you are a passionate and innovative engineering professional with experience in medical device development and a strong background in vision correction technologies, we encourage you to apply for the Vision Correction Device Design Engineer role in Irvine, CA. This is a unique opportunity to contribute to cutting-edge ophthalmic solutions that positively impact patients’ lives.
To apply, please submit your resume and a cover letter detailing your experience in:
Designing and developing medical devices or vision correction systems
Working within FDA/ISO-compliant environments
Engineering product innovation from concept through commercialization
Collaborating cross-functionally with R&D, clinical, and manufacturing teams
Be sure to highlight specific projects, technologies, or regulatory environments you’ve worked in, especially those related to ophthalmology, optomechanics, or wearable medical devices.
This role offers a high-impact opportunity to be part of a collaborative, mission-driven team that is shaping the future of vision correction through engineering innovation. Apply today to join a company where your contributions will directly advance healthcare outcomes.
For more information or to explore similar roles in medical technology, visit our Medical Device Engineering Careers page.
Tags:
Vision Correction Engineer | Medical Device Design | Ophthalmic Devices | Biomedical Engineering Jobs | FDA Regulated Engineering | Product Development | Optics & Vision Innovation | Engineering Jobs in Irvine CA
