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9 results (3 new)

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Developement Engineer

Synkriom

Hybrid in Warsaw, Indiana • Today

Easy Apply

Full-time

$35 - $38

Medical Device Project Manager

Synkriom

Warsaw, Indiana • Today

Easy Apply

Contract

Depends on Experience

Sr. Business Analyst - Medical Devices

NexInfo Solutions, Inc.

Remote • 9d ago

Easy Apply

Contract

$80 - $90

Windchill Solution Architect - Medical Device experience

EdgeAll

Remote • Today

Easy Apply

Third Party, Contract

$70 - $80

Medical Device Software Project Manager

APN Software Services, Inc

Remote • Yesterday

Easy Apply

Contract

Depends on Experience

Field Service Engineer III

TransMedics

Remote • Today

Full-time

USD 80,000.00 - 113,000.00 per year

Medical Devices Software Engineering Project Manager - Ultrasound , SAFe Agilist (SA), SAFe Scrum Master (SSM), or PMP.

APN Software Services, Inc

Remote • Today

Easy Apply

Contract

70 - 80

Sr Talent Acquisition Specialist - Medical Devices

Ledgent Technology

Remote or Hybrid • Today

Easy Apply

Contract

$45.00 - $51.00 per hour

Medical Device V&V engineers

Katalyst Healthcares and Lifesciences

Remote or New Jersey • 14d ago

Full-time

Job Details

Skills

Biomedical Engineering
Design Of Experiments
ISO 9000
ISO 13485
Medical Devices
Product Development
21 CFR Part 820 QSR (2024)
MDD and MDR

Summary

Job Description

We are seeking a qualified Medical Device Engineer with experience in regulated medical device product development, engineering studies, and medical device standards. The ideal candidate will have strong technical writing and communication skills, knowledge of quality and regulatory requirements, and experience applying statistical methods to engineering studies.

Required Qualifications

Bachelor's degree in Engineering with at least 3 years of relevant experience, or equivalent experience.
Strong written and verbal communication skills.
Proficiency in Microsoft Office Suite.
Working knowledge of medical device standards and regulations, including:
- 21 CFR Part 820 QSR (2024)
- ISO 13485
- ISO 14971
- MDD and MDR
- IEC 62366-1
- ISO/IEC 27001
- BS EN 62304
Working knowledge of statistics applied to engineering studies, including sample size rationale, DOE, and hypothesis testing.
Preferred Qualifications
- 3 5 years of full-time engineering experience in regulated medical device product development.
- Degree from an ABET-accredited institution, or global equivalent, in Mechanical Engineering, Biomedical Engineering, Bioengineering, Materials Science, Materials Engineering, Chemical Engineering, Polymer Engineering, or a related engineering discipline.
- Experience with orthopedic implants, medical software, biomaterials, antimicrobial technologies, wound management, coatings, or local drug delivery.
- Familiarity with drug-device combination products and Software as a Medical Device (SaMD).
- Experience with Minitab and statistical analysis.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 90944144
Position Id: 9122881
Posted 18 hours ago

Fitment

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Similar Jobs

Principal Engineer, Systems Engineering

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Work Flexibility: Hybrid or Onsite Stryker is seeking a dynamic and visionary product development leader with a proven track record of leading large, complex product development programs through the application of systems engineering principles. As the technical quarterback, this individual will drive alignment, collaboration, and execution across a multidisciplinary global product line, ensuring teams work cohesively toward shared objectives while delivering innovative solutions that improve p

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Principal Engineer, R&D

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Job Description Support and lead the development of medical device products, including writing or verifying specifications; maintaining product process; designing fixtures; and testing processes, equipment, and raw materials to ensure the concepts and/or prototypes meet their requirements. Job duties:Develop new product concepts and products by applying various engineering disciplines, such as mechanical, electrical, materials, bioengineering, or other relevant fields2. Provide engineering desi

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Senior Mechanical Engineer

Portage, Michigan

•

Today

Work Flexibility: Hybrid Senior Mechanical Design EngineerPortage, MI Join Stryker's Orthopaedic Instruments team and contribute to the development of mechanical and electromechanical products used in surgical environments. This role offers the opportunity to work across the full product development lifecycle, from concept generation and prototyping through design verification, manufacturing scale-up, and product launch. You will collaborate with cross-functional teams while applying engineeri

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Sr Engineer, R&D

No location provided

•

Today

Job Description Support development of products and/or product engineering for medical device with work including writing or verifying specifications; designing new products and fixtures; testing processes and equipment; and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Job duties:Develop new product concepts and products by applying various engineering disciplines, such as mechanical, electrical, materials, bioengineering, or other relevant fields.

Full-time

Job Details

Skills

Biomedical Engineering
Design Of Experiments
ISO 9000
ISO 13485
Medical Devices
Product Development
21 CFR Part 820 QSR (2024)
MDD and MDR

Summary

Job Description

Required Qualifications

Bachelor's degree in Engineering with at least 3 years of relevant experience, or equivalent experience.
Strong written and verbal communication skills.
Proficiency in Microsoft Office Suite.
Working knowledge of medical device standards and regulations, including:
- 21 CFR Part 820 QSR (2024)
- ISO 13485
- ISO 14971
- MDD and MDR
- IEC 62366-1
- ISO/IEC 27001
- BS EN 62304
Working knowledge of statistics applied to engineering studies, including sample size rationale, DOE, and hypothesis testing.
Preferred Qualifications
- 3 5 years of full-time engineering experience in regulated medical device product development.
- Degree from an ABET-accredited institution, or global equivalent, in Mechanical Engineering, Biomedical Engineering, Bioengineering, Materials Science, Materials Engineering, Chemical Engineering, Polymer Engineering, or a related engineering discipline.
- Experience with orthopedic implants, medical software, biomaterials, antimicrobial technologies, wound management, coatings, or local drug delivery.
- Familiarity with drug-device combination products and Software as a Medical Device (SaMD).
- Experience with Minitab and statistical analysis.

Dice Id: 90944144
Position Id: 9122881
Posted 18 hours ago

Fitment

Dice Job Match Score™

To see how well you match this job, please log in or create an account.

Once logged in, be sure to complete your profile to get the most accurate match score.

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

Principal Engineer, Systems Engineering

Portage, Michigan

•

Today

Full-time

USD 118,000.00 - 196,700.00 per year

Principal Engineer, R&D

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Senior Mechanical Engineer

Portage, Michigan

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USD 77,700.00 - 129,500.00 per year

Sr Engineer, R&D

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