1

Europe Biomedical Engineer Jobs (NOW HIRING)

Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or ... Ability to travel internationally (Europe + Asia) (15%). * Authorized to work in the United States ...

Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more ... Associates Degree in Electronics, Biomedical Engineering, Medical Technology or related industry.

Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more ... Associates Degree in Electronics, Biomedical Engineering, Medical Technology or related industry.

Quality Engineer

Rochester, NY · On-site

$74K - $94K/yr

Headquartered in Ilminster Somerset, UK with primary operations in the USA and Europe, G&H is ... biomedical, healthcare diagnostics, machine vision and analytical instrument markets, as well as ...

Quality Engineer

Rochester, NY · On-site

$74K - $94K/yr

Headquartered in Ilminster Somerset, UK with primary operations in the USA and Europe, G&H is ... biomedical, healthcare diagnostics, machine vision and analytical instrument markets, as well as ...

next page

Showing results 1-20

Europe Biomedical Engineer information

See salary details

$41K

$94.8K

$140K

How much do europe biomedical engineer jobs pay per year?

As of Jun 12, 2026, the average yearly pay for europe biomedical engineer in the United States is $94,807.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $116,000.00 per year, depending on experience, location, and employer.

How does a Europe Biomedical Engineer typically collaborate with healthcare professionals and equipment suppliers?

As a Europe Biomedical Engineer, you will frequently interact with doctors, nurses, and technicians to understand their equipment needs, provide technical support, and ensure devices function safely and efficiently. You’ll also coordinate with equipment suppliers for procurement, installation, and maintenance, acting as a technical bridge to resolve issues and implement upgrades. This collaborative approach not only improves patient care but also helps you stay updated on the latest medical technology. Effective communication and teamwork are essential for success in this role.

What does a Europe Biomedical Engineer do?

A Europe Biomedical Engineer designs, develops, and maintains medical equipment and devices used in healthcare settings across Europe. They work on improving the safety, efficiency, and effectiveness of medical technologies, collaborating with doctors, nurses, and other healthcare professionals. Their role also involves ensuring that equipment complies with European regulatory standards and conducting training or support for medical staff. Biomedical engineers may also participate in research and development to innovate new medical solutions tailored to the needs of European healthcare systems.

What are the key skills and qualifications needed to thrive as a Europe Biomedical Engineer, and why are they important?

To thrive as a Europe Biomedical Engineer, you generally need a degree in biomedical engineering or a related field, a strong grasp of medical device regulations (such as MDR), and proficiency in engineering principles. Familiarity with CAD software, laboratory instrumentation, and regulatory compliance tools is typically required, along with certifications like CE marking knowledge. Excellent problem-solving abilities, teamwork, and clear communication are crucial soft skills for collaborating with clinicians and cross-functional teams. These skills and qualifications ensure the safe design, maintenance, and regulatory compliance of medical technologies essential for patient care and healthcare innovation.

What is the difference between Europe Biomedical Engineer vs Europe Medical Device Technician?

AspectEurope Biomedical EngineerEurope Medical Device Technician
Required CredentialsBachelor's or Master's in Biomedical Engineering, certifications in medical device regulationTechnical diploma or certification in medical device technology, specialized training
Work EnvironmentResearch labs, hospitals, medical device companiesHospitals, clinics, repair centers
Employer & Industry UsageMedical device manufacturers, healthcare institutions, research organizationsHospitals, medical equipment service providers
Common Search & ComparisonOften compared for roles in device development and designCompared for hands-on maintenance and repair roles

The Europe Biomedical Engineer typically focuses on designing, developing, and testing medical devices, requiring advanced engineering credentials. In contrast, the Europe Medical Device Technician specializes in maintaining, repairing, and servicing medical equipment, often with technical certifications. Both roles are vital in healthcare but differ in their focus, work environment, and required qualifications.

Infographic showing various Europe Biomedical Engineer job openings in the United States as of June 2026, with employment types broken down into 3% Internship, 2% As Needed, 75% Full Time, 15% Part Time, 3% Temporary, and 2% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $94,807 per year, or $45.6 per hour.

Program Manager, Wellness

Helenoftroy

Marlborough, MA • Hybrid

$88K - $110K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago


Job description

Join our Wellness team at Helen of Troy and make an immediate impact on our trusted brands: Honeywell, PUR, Braun, Vicks. Together, we build innovative and useful products that elevate people's lives everywhere every day.

Look around your home, and you'll find us everywhere, in your kitchen, living room, bedroom, and bathroom. We are already making your everyday lives better. We are powered by knowledgeable, enthusiastic, and forward-thinking people committed to developing a culture of inclusion. Whether you are just starting your career or in need of a challenge, we recognize, develop, and empower talent!

Position: Program Manager, Wellness

Department: Wellness (Honeywell, PUR, Braun, Vicks)

Work Location: Marlborough MA, Hybrid (work 3 days onsite)

Hybrid Schedule: At Helen of Troy, we embrace a flexible hybrid work model designed to support collaboration and productivity. For roles eligible for hybrid work, our standard schedule includes in-office collaboration from Tuesday through Thursday, with the option to work remotely on Mondays and Fridays. Any updates to this model will be communicated in advance. Please note that hybrid eligibility and schedules may vary based on business needs and manager expectations.

What you will be doing:

The Program Manager, Wellness role requires managing healthcare and wellness New Product Development programs from concept to production. The ideal candidate will have experience in developing consumer, electromechanical products and managing multiple programs on a global basis. This role requires the ability to identify issues, assess technical/program alternatives, and manage risks while keeping programs on track.

  • Take a supporting/lead role in planning, scheduling, and executing New Product Development (NPD) programs in collaboration with suppliers and internal teams.

  • Utilize Helen of Troy New Product Development process to effectively drive program progress and manage risks. Familiarity with Agile process is a plus.

  • Work closely with global cross-functional teams in US, Europe, and China. Communicate to teams effectively on program progress, risks, schedule, costs, quality, and performance.

  • Responsible for technical feasibility assessment, program budget, program schedule, and supplier communication.

  • Manage/create product documentation and specifications to support timely execution.

  • Provide guidance for technical solutions and conduct design reviews, FMEA's (Failure Mode and Effect Analysis), and risk assessments.

  • Create and maintain accessible program files (Design History File) and appropriate documentation based on established regulatory and quality systems

Skills needed to be successful in this role:

  • Demonstrated abilities with designing and manufacturing consumer and/or medical devices.

  • Leadership and teamwork skills to interact with a cross-functional global team and direct them in achieving assigned goals and objectives.

  • Ability to handle multiple programs while remaining flexible and adaptable.

  • Demonstrated delivery of programs within budget and schedule constraints in a fast-paced environment.

  • Demonstrated ability to work independently.

  • Ability to collaborate with multiple global vendors and coordinate submittals, track vendor commitments on a schedule, and oversight of delivering quality products.

  • Strong communication skills including ability to provide concise and accurate status of programs on a weekly basis.

  • Demonstrated troubleshooting ability to identify issues, assess technical and program alternatives while managing risks to keep programs on track.

Minimum Qualifications:

  • Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or equivalent.

  • 3+ years of experience working in consumer goods, medical, or any equivalent regulated industry.

  • Good technical knowledge of plastic part design, electronics, firmware, and software as used in consumer products.

  • Proven track record in program management, demonstrating strong organizational skills and attention to details.

  • Proficient in Microsoft Office Programs (MS Excel, Project, Outlook, Word).

  • Working knowledge of FDA, ISO, UL, and Design History Files.

  • Basic knowledge of CAD.

  • Ability to join virtual meetings in the early morning or evening for international calls as needed outside standard business hours

  • Ability to travel internationally (Europe + Asia) (15%).

  • Authorized to work in the United States on a full-time basis.

Preferred Qualification:

  • Working knowledge of IEC 62304

  • Understanding of safety requirements and medical device regulatory submission in Europe (MDD/MDR) and USA (FDA).

In Massachusetts, the standard base pay range for this role is $88,000 - 110,000 annually. This base pay range is specific to Massachusetts and may notbe applicableto other locations. Actual salaries will vary based on several factors, including but not limited to location, experience, skill level, and performance.

The range listed is just onecomponentof the total compensation package for employees.

Benefits:Salary + Bonus,Healthcare, Dental, Vision, Paid Holidays, Paid Parental Leave, 401(k) with company match, Basic Life Insurance, Short Term Disability (STD), Long Term Disability (LTD), Paid Time Off (PTO), Paid Charitable (volunteer) Leave, and Educational Assistance.

Wondering if you should apply? Helen of Troy welcomes people as diverse as our brands! Have the confidence tocome aswho you are because your point of view, skills, and experience will make us stronger. Ifyou'reeager to sharenew ideasand try new things, we want to hear from you.

#li-ab1

#LI-HYBRID

For more information about Helen of Troy, visit www.helenoftroy.com. You can also find us on LinkedIn, and Glassdoor.

Helen of Troy is an Equal Opportunity/Affirmative Action Employer. We are committed to developing a diverse workforce and cultivating an inclusive environment. We value diversity and believe that we are strengthened by the differences in our experiences, thoughts, cultures, and backgrounds. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category under applicable federal, state, and local laws.

We will provide individuals with disabilities with reasonable accommodations to participate in the job application process. If you would like to request an accommodation, please contact Human Resources at (915) 225-8000.

Founded in 1968, Helen of Troy is a prominent player in the global consumer products industry, offering diverse career opportunities across North America, South America, Europe, and Asia. We boast a collection of renowned brands such as OXO, Hydro Flask, Osprey, Honeywell, PUR, Braun, Vicks, Hot Tools, Drybar, Curlsmith, Revlon, and Olive & June - many of which rank #1, #2, or #3 in their respective categories, making the Helen of Troy name synonymous with excellence and ingenuity.

At Helen of Troy, our strategy involves acquiring brands that we can integrate and enhance, amplifying their unique attributes to drive growth and profitability. Embracing a culture of collaboration internally and externally, we are committed to providing innovative solutions tailored to consumers, operational excellence, global scalability, and exceptional shared services to support our brand portfolio. This dedication to fostering development and success sets Helen of Troy apart as a pioneer in the industry, propelling our brands to unparalleled heights of success and recognition worldwide.

The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities and duties required of personnel so classified. Management retains the right to add or to change duties of the position at any time.