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Evening Medical Device Design information

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How much do evening medical device design jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for evening medical device design in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What is an Evening Medical Device Design job?

An Evening Medical Device Design job involves creating, developing, and testing medical devices during evening or non-traditional work hours. Professionals in this role typically work on the design and improvement of medical equipment, collaborating with engineers, clinicians, and regulatory experts to ensure devices are safe, effective, and compliant with industry standards. This schedule can be ideal for those seeking flexibility or companies operating on extended shifts. Responsibilities may include CAD modeling, prototyping, documentation, and product testing. Evening roles are common in organizations needing round-the-clock development or support for critical healthcare projects.

What is the difference between Evening Medical Device Design vs Night Medical Device Design?

AspectEvening Medical Device DesignNight Medical Device Design
Work HoursTypically evening shifts, often from 2 PM to 10 PMPrimarily night shifts, usually from 10 PM to 6 AM
Work EnvironmentDesign labs and offices with daytime supportDesign labs with overnight team collaboration
CertificationsRelevant engineering or design certifications, FDA knowledgeSame as Evening Medical Device Design, with additional night shift safety protocols

Both roles involve designing medical devices, but the main difference lies in shift timing. Evening Medical Device Design professionals work during late afternoons and evenings, while Night Medical Device Design roles focus on overnight hours. The core skills, certifications, and industry usage are similar, with shift hours being the primary distinction.

What are some common challenges faced when working evening shifts in medical device design teams?

Working evening shifts in medical device design can present unique challenges, such as coordinating effectively with cross-functional teams who may be on daytime schedules and ensuring timely communication regarding project updates or urgent issues. Additionally, there can be fewer on-site resources or support staff available during evening hours, requiring greater independence and proactive problem-solving. However, evening shifts can also offer a quieter environment for focused design work and may provide opportunities to handle urgent tasks that arise outside of regular hours, demonstrating reliability and adaptability to managers.

What key skills and qualifications are needed to thrive as an Evening Medical Device Design Engineer, and why are they important?

To excel in Evening Medical Device Design, you need a solid background in biomedical engineering or a related field, with expertise in device design principles and compliance with medical regulations. Familiarity with CAD software, prototyping tools, and relevant quality management systems (such as ISO 13485) is typically required. Strong problem-solving skills, attention to detail, and effective communication are crucial for collaborating with cross-functional teams and addressing design challenges. These competencies ensure the creation of safe, effective devices that meet regulatory standards and improve patient outcomes.
What cities are hiring for Evening Medical Device Design jobs? Cities with the most Evening Medical Device Design job openings:
What are the most commonly searched types of Medical Device Design jobs? The most popular types of Medical Device Design jobs are:
What states have the most Evening Medical Device Design jobs? States with the most job openings for Evening Medical Device Design jobs include:
Evening Medical Device Design jobs near you
Senior Engineer I, Device Development

Senior Engineer I, Device Development

Alexion Pharmaceuticals

Fresno, CA • On-site

$97K - $146K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Location: Boston, MA or New Haven, CT

This is what you will do:
This position will serve the role of Development Engineer within the Alexion Device Development organization.
The candidate will act as the technical SME/project engineer supporting the development of combination products.
This role will be accountable for key technical design and development deliverables.
This individual will interact with multiple functions and functional teams including Device Quality, Regulatory Affairs, Clinical, Global Technical Operations (GTO), and Alexion Dublin Manufacturing Facility (ADMF) from clinical development through commercial development.
You will be responsible for:
Deep understanding of the device design: this may include development/ identification of critical dimensions, systems engineering, sensitivity analysis, tolerance stack-ups.

Technical assessments to be conducted via analytical and empirical means.

Devices of interest include: pre-filled syringes, autoinjectors, pen injectors, and on-body delivery systems.

Based on understanding of device design, manage facets of technical development. This can include interactions with suppliers, CMOs, technology vendors and/or internal cross-functional teams.

Oversee the characterization and design verification testing as well as determine relevant success criteria. This includes development, qualification, and the transfer of the appropriate methods.

Author technical documentation in support of the development process or design control deliverables.

Root Cause analysis of product or process deviations or failures. Utilization of six sigma tools to manage the investigation.

Ability to clearly communicate learnings and educate other team members on methods and analytical approaches.

Acts independently within team expectations, coordinates with functional leadership to identify priorities, completes tasks under his/her accountability while balancing a high level of autonomy .

Demonstrate technical rigor and creativity, continuous learning and improvement, and alignment to customer needs and value creation.

Demonstrate strong and clear accountability/responsibility for successful and timely completion of designated tasks.
You will need to have:
BS Degree (Mechanical, Biomedical, Chemical Engineering or Materials Science and Engineering)or closely related disciplines

6+ years of experience as a product design/development engineer in the medical device or pharmaceutical industries or related experience (experience with combination products, specifically prefilled syringes, autoinjectors, pen injectors, and on-body injectors preferred).

Experience with developing products or implementing product changes through a structured, phase-gated, product development process.

Demonstrated experience with all phases of the Design Control process.
Demonstrated experience in a technical, product development role on a cross-functional team, leadership role preferred.

Understanding of medical device product development risk management methodologies.

Possesses expertise in statistical analysis (Minitab, Crystal Ball, etc), analytical tools (e.g. FEA), benchtop testing (e.g. Zwick, fixture design) and experience in root cause analysis/investigation

Strong team building and collaboration skills across the organization. Possesses intellectual curiosity to deeply understand technical concepts.

Knowledge of performance and regulatory compliance (EU and FDA) requirements of medical device and combination products (e.g. IEC 62366, ISO 11608 series, ISO 14971, IEC 60601 series, FDA QSR 21 CFR Part 4 and 820 / ISO13485 quality system requirements).

The duties of this role are generally conducted in an office environment.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:
Master's, or PhD Degree in Engineering(Mechanical, Biomedical, Chemical or Materials Science and Engineering)or closely related disciplines preferred.

6-10+ years of experience inmedical device/container closure development with 2+ years in combination product commercialization.

The annual base salary for this position ranges from $97,000 to $146,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles) or to receive a retirement contribution (hourly roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Date Posted

08-Jun-2026

Closing Date

09-Jul-2026

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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