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Medical Device Development Technical Advisor Jobs

Senior Engineer II, Device Development

Cambridge, MA · On-site

$114K - $156K/yr

Lead technical issues to resolution by documenting investigations, performing root cause analysis ... You have experience developing medical devices and/or combination products for new product ...

Biotech & Medical Device Coach

$19.25 - $26/hr

... and development, medical device development, and medical device manufacturing, as well as ... technical interviews, as well as guidance on salary negotiation and freelancing for students ...

$102K - $141K/yr

The Device engineer will be responsible for design, prototyping, technical analysis, and testing of ... Experience in a regulated laboratory (pharma, biotech, medical device, mechanical, or environmental)

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Ability to read and follow work instructions, BOMs, and technical drawings * Strong attention to ... Excel Medical Products is a trusted name in the medical device manufacturing industry, proudly ...

Medical Device Assembly

Wixom, MI · On-site

$16 - $17/hr

Ability to read and follow work instructions, BOMs, and technical drawings * Strong attention to ... Excel Medical Products is a trusted name in the medical device manufacturing industry, proudly ...

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Medical Device Development Technical Advisor information

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How much do medical device development technical advisor jobs pay per year?

As of Sep 11, 2026, the average yearly pay for medical device development technical advisor in the United States is $114,963.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Medical Device Development Technical Advisor jobs?

For Medical Device Development Technical Advisor jobs, the most frequently searched job titles are:

Infographic showing various Medical Device Development Technical Advisor job openings in the United States as of July 2026, with employment types broken down into 93% Full Time, 6% Part Time, and 1% Contract. Highlights an 72% Physical, 3% Hybrid, and 25% Remote job distribution, with an average salary of $114,963 per year, or $55.3 per hour.

Human Factors Engineer 3, Device Development

Boston, MA • On-site

AstraZeneca
Pharmaceutical Product Wholesalers • 10K+ employees

$101K - $133K/yr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz


Job description

This is what you will do:

This position will serve the role of Engineer III for device development / human factors engineering within the Alexion Device Development organization. The role will support the human factors workstreams for pipeline products as well as lifecycle management. This role will interact with multiple functional teams including Device Development, Clinical, Commercial/Marketing, Quality, and Regulatory, clinical development through registration and commercial product support.

You will be responsible for:
  • Lead and support activities under the human factors and usability engineering process for combination product design and development from feasibility, clinical development through registration and post-market.
  • Support core teams to develop and support the strategy for human factors/ usability engineering activities from formative studies to final HF validation for combination products.
  • Support design validation activities including summative human factors study (i.e. human factors validation) from protocol development, study execution, and reporting.
  • Provide feedback and/or author for user need identification and user interface specifications development.
  • Provide feedback to use-related risk management activities such as known use problem analysis, hazard analysis, and use-related risks analysis
  • Draw findings from competitive analysis, market sensing, complaint handling to inform new product design (inclusive of device, labeling and secondary packaging)
  • Collaborate with human factors firms (vendors) and manage their activities for a formative or summative human factors study.
  • Communicate effectively, both verbally and in writing, internally across departments and with external suppliers.
  • Ensure all human factors engineering activities as required and comply with the Company’s quality assurance requirements as well as applicable regulatory requirements.
  • Support feasibility activity of device assessment (e.g., testing, fixturing, protocol, report).
You will need to have:
  • Experience in human factors engineering and exposure to design and development of medical device and combination products.
  • Experience in design control activities.
  • Ability to manage external human factors firms (vendors).
  • Strong communication and collaboration skills; ability to connect with all levels of the organization. Proficient in writing internal reports, project summaries, and internal/external presentations.
  • Knowledge of human factor/usability engineering, safety, performance and regulatory compliance requirements of medical device and combination products (e.g. IEC 62366, FDA HF guidances, EU Regulation 2017/745 (MDR)).
  • [For office-based positions:] As is typical of an office-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.
We would prefer for you to have:
  • Bachelor’s or Master’s degree in Engineering (Biomedical, Chemical, Mechanical, Electrical Engineering or Human Factors) plus 3-6 years experience in medical device Human Factors development and design control.
  • Experience with injection based combination product development and risk management preferred.
  • Experience with graphics design a plus.

Joining Alexion means embracing an opportunity where work isn’t ordinary. We are a beacon in the global Biopharmaceutical landscape. Our closeness to patients brings us closer to our work and each other. Combined with our brave, pioneering spirit – we are truly unique in R&D and healthcare. At Alexion, grow and innovate in a business with a rapidly expanding portfolio. Enjoy the entrepreneurial spirit of a leading biotech while meeting the needs of some of the most under-served patients in the world. You will be empowered with tailored development programs designed not just for skill enhancement but for fostering a deep understanding of our patient's journeys. Supported by outstanding leaders and peers ready to lift you in marketing, compliance, and beyond.

The annual base pay (or hourly rate of compensation) for this position ranges from $101,643.20 to $133,406.70. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB