We are seeking engineers with SaMD (Software as a Medical device) in technical capacity which can include product design, development and/or testing. Purpose of the position To build, manage, develop ...
We are seeking engineers with SaMD (Software as a Medical device) in technical capacity which can include product design, development and/or testing. Purpose of the position To build, manage, develop ...
Design Quality Engineer
Indianapolis, IN · On-site +1
The Design Quality Engineer will play a crucial role in supporting quality activities throughout the medical device product development lifecycle. This position requires a strong understanding of ...
Design Quality Engineer
Indianapolis, IN · On-site +1
The Design Quality Engineer will play a crucial role in supporting quality activities throughout the medical device product development lifecycle. This position requires a strong understanding of ...
Engineering Manager
Warsaw, IN · On-site
$110 - $150/hr
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...
Engineering Manager
Warsaw, IN · On-site
$110 - $150/hr
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...
Be Seen First
Medical Device Quality Engineer
Warsaw, IN · On-site
$35 - $40/hr
... design assurance, FMEA, and product testing methods, and are able to use optical comparators and ... Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience ...
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Be Seen First
Medical Device Quality Engineer
Warsaw, IN · On-site
$35 - $40/hr
... design assurance, FMEA, and product testing methods, and are able to use optical comparators and ... Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience ...
New
Design Quality Engineer
Warsaw, IN · On-site
... Month Contract Position Overview We are seeking a Design Quality Engineer to support product development, validation, and lifecycle management activities within a medical device environment. This ...
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Design Quality Engineer
Warsaw, IN · On-site
... Month Contract Position Overview We are seeking a Design Quality Engineer to support product development, validation, and lifecycle management activities within a medical device environment. This ...
Senior R&D Engineer - MediTech (Mitsubishi Chemical Advanced Materials)
Fort Wayne, IN · On-site
$101 - $126/hr
Experience with medical device design controls (21 CFR 820.30) * Knowledge of FDA Quality System Regulations and ISO 13485 * Experience with ISO 10993 biocompatibility standards * Knowledge of ISO ...
Senior R&D Engineer - MediTech (Mitsubishi Chemical Advanced Materials)
Fort Wayne, IN · On-site
$101 - $126/hr
Experience with medical device design controls (21 CFR 820.30) * Knowledge of FDA Quality System Regulations and ISO 13485 * Experience with ISO 10993 biocompatibility standards * Knowledge of ISO ...
Experience with medical device design controls (21 CFR 820.30) * Knowledge of FDA Quality System Regulations and ISO 13485 * Experience with ISO 10993 biocompatibility standards * Knowledge of ISO ...
Experience with medical device design controls (21 CFR 820.30) * Knowledge of FDA Quality System Regulations and ISO 13485 * Experience with ISO 10993 biocompatibility standards * Knowledge of ISO ...
Experience with medical device design controls (21 CFR 820.30) * Knowledge of FDA Quality System Regulations and ISO 13485 * Experience with ISO 10993 biocompatibility standards * Knowledge of ISO ...
Experience with medical device design controls (21 CFR 820.30) * Knowledge of FDA Quality System Regulations and ISO 13485 * Experience with ISO 10993 biocompatibility standards * Knowledge of ISO ...
Senior Software Engineer for Medical Device Startup
Fishers, IN · On-site
$114K - $151K/yr
Design intuitive and visually engaging user interfaces. * Proactively take on new responsibilities ... Experience working in the medical device industry. * Familiarity with Agile development ...
Senior Software Engineer for Medical Device Startup
Fishers, IN · On-site
$114K - $151K/yr
Design intuitive and visually engaging user interfaces. * Proactively take on new responsibilities ... Experience working in the medical device industry. * Familiarity with Agile development ...
Senior Software Engineer for Medical Device Startup
Fishers, IN · On-site
$115K - $152K/yr
Design intuitive and visually engaging user interfaces. * Proactively take on new responsibilities ... Experience working in the medical device industry. * Familiarity with Agile development ...
Quick apply
Senior Software Engineer for Medical Device Startup
Fishers, IN · On-site
$115K - $152K/yr
Design intuitive and visually engaging user interfaces. * Proactively take on new responsibilities ... Experience working in the medical device industry. * Familiarity with Agile development ...
Senior Software Engineer for Medical Device Startup
Fishers, IN · On-site
$90 - $120/hr
Design intuitive and visually engaging user interfaces. * Proactively take on new responsibilities ... Experience working in the medical device industry. * Familiarity with Agile development ...
Senior Software Engineer for Medical Device Startup
Fishers, IN · On-site
$90 - $120/hr
Design intuitive and visually engaging user interfaces. * Proactively take on new responsibilities ... Experience working in the medical device industry. * Familiarity with Agile development ...
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Design and execute experimental studies, including study planning, hypothesis generation, and ...
Quick apply
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Design and execute experimental studies, including study planning, hypothesis generation, and ...
Sr Manufacturing Engineer- Medical Device at Master Compliance Warsaw, IN
Warsaw, IN · On-site
$95 - $135/hr
Job Location - Warsaw, Indiana (Fully On Site.) Type - Contract ( W2 Only ). Duration - 12 Months ... Tooling & Equipment Design * Experience designing fixtures, gages, cutting tools , and implementing ...
Sr Manufacturing Engineer- Medical Device at Master Compliance Warsaw, IN
Warsaw, IN · On-site
$95 - $135/hr
Job Location - Warsaw, Indiana (Fully On Site.) Type - Contract ( W2 Only ). Duration - 12 Months ... Tooling & Equipment Design * Experience designing fixtures, gages, cutting tools , and implementing ...
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Design and execute experimental studies, including study planning, hypothesis generation, and ...
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation ... Design and execute experimental studies, including study planning, hypothesis generation, and ...
Silkscreen Operator
Indianapolis, IN · On-site
$16.25 - $19.25/hr
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...
Silkscreen Operator
Indianapolis, IN · On-site
$16.25 - $19.25/hr
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...
Design Quality Engineer
Indianapolis, IN · On-site
Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control requirements. • Knowledge of FDA 21 CFR Part 820, ISO ...
Design Quality Engineer
Indianapolis, IN · On-site
Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control requirements. • Knowledge of FDA 21 CFR Part 820, ISO ...
Engineering Manager
Warsaw, IN · On-site
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...
Engineering Manager
Warsaw, IN · On-site
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...
Design Quality Engineer
Indianapolis, IN · On-site
Location: ~Indianapolis, IN~ (REMOTE) Duration: 6 months Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control ...
Design Quality Engineer
Indianapolis, IN · On-site
Location: ~Indianapolis, IN~ (REMOTE) Duration: 6 months Design Quality Engineer Technical/Functional Skills • Strong understanding of Medical Device Product Development Process and Design Control ...
Solution Design & Verification * Lead solution design, specification development, verification, and validation activities. * Define solution packages, components, and elements at the required level ...
New
Quick apply
Solution Design & Verification * Lead solution design, specification development, verification, and validation activities. * Define solution packages, components, and elements at the required level ...
New
Quality Engineer
Noblesville, IN · On-site
$67K - $87K/yr
Quality Assurance Department: QA, Noblesville Employment Type: Full-time Req ID: 9887 We are seeking a Quality Engineer with experience in medical device design quality and risk management to support ...
Quality Engineer
Noblesville, IN · On-site
$67K - $87K/yr
Quality Assurance Department: QA, Noblesville Employment Type: Full-time Req ID: 9887 We are seeking a Quality Engineer with experience in medical device design quality and risk management to support ...
Contract Medical Device Design information
What is the difference between Contract Medical Device Design vs Medical Device Design Engineer?
| Aspect | Contract Medical Device Design | Medical Device Design Engineer |
|---|---|---|
| Credentials | Typically requires a degree in engineering or related field; certifications like ISO 13485 are a plus | Requires a degree in biomedical, mechanical, or electrical engineering; professional certifications may enhance prospects |
| Work Environment | Project-based, often freelance or consulting; varies by client and project scope | Full-time employment within a company or R&D department |
| Employer & Industry Usage | Used by consulting firms, contract agencies, and medical device startups | Employed by medical device companies, hospitals, or research institutions |
Contract Medical Device Design professionals focus on project-specific work, often freelance, while Medical Device Design Engineers are typically employed full-time within organizations. Both roles require similar technical credentials but differ in work setting and employment structure.
What are the most commonly searched types of Medical Device Design jobs in Indiana?
The most popular types of Medical Device Design jobs in Indiana are:
What are popular job titles related to Contract Medical Device Design jobs in Indiana?
For Contract Medical Device Design jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Contract Medical Device Design jobs in Indiana look for?
The top searched job categories for Contract Medical Device Design jobs in Indiana are:
- Medical Device Sales Internship
- Commission Cardiac Device Sales
- Neuromodulation Sales
- Locum Medical Device Design
- Human Factors Engineer Medical Device
- Remote 1099 Medical Device Sales
- Afternoon Medical Device Startup
- Orthopedic Medical Device Sales
- Internship Orthopedic Device Sales
- Medical Device Territory Manager
What cities in Indiana are hiring for Contract Medical Device Design jobs?
Cities in Indiana with the most Contract Medical Device Design job openings:
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 28 days ago
Job description
We exist to create positive change for people and the planet. Join us and make a difference too!
Job Title:Technical Specialist, Scheme Manager, Clinical Evaluation Specialist - SaMD
Reports to: Technical Team Manager
Location:Home Based - Global
We have exciting opportunities for medical device software specialists to join our Software team. You will have the opportunity to work with medical device manufacturers across the globe, from dynamic start-ups through to established large manufacturers. We are seeking engineers with SaMD (Software as a Medical device) in technical capacity which can include product design, development and/or testing.
Purpose of the position
To build, manage, develop, control and manage a portfolio of Medical Device CE marking schemes. To deliver technical documentation assessments in support of the CE marking schemes. To provide Medical Device expertise leadership and mentoring in areas of competence to Healthcare personnel.
Key Responsibilities & Accountabilities
Plan and deliver Technical File Assessments, Design Examinations and Unannounced Audits to support EC Certification.
Manage client projects, acting as their primary contact and after satisfactory assessment, to make certification recommendations for CE, UKCA and ISO 13485 certificate issue to ensure compliance with required certification, timely delivery of services and client satisfaction.
Act as technical support to the commercial team when required to support business development and marketing activities as it grows the customer base worldwide.
Perform unannounced visits to medical device manufacturers globally as a technical expert to check on compliance with certification.
Work with Line Manager and other team leaders as required to provide reviews within area of expertise.
Essential Criteria:
4 or more years of Software Medical Device experience in a technical capacity, preferably within product design, development and/ or testing.
Interpretation and applications of International and National standards for the design, development and regulation of software medical devices.
Understanding of Risk Management and FMEA of Software Medical Devices.
Broad technical understanding of medical devices. Understanding of companies operating in these spaces and current industry trends.
Qualifications:
Degree educated (Bachelor's minimum or equivalent) relevant to medical device design, development, manufacture and use i.e. electro-mechanical, electronic/electrical, biomedical engineering, computer science, medical physics or similar
BSI offers a competitive total reward package, an independent and varied job in an international environment, flexible working hours, ongoing training and development. For the US, this role offers 20-days annual leave, bank holidays, medical, dental, vision, and life insurance, 401(K) with company contribution, short-term and long-term disability, maternal leave, paid parental leave, paid bereavement leave, learning and development opportunities, and a wide range of flexible benefits that you can tailor to suit your lifestyle.As the salary differs per country according to various factors, if you reside in another country, you'll be notified of the salary range by the recruiter.
Do you believe the world deservesexcellence?
We are proud to be the business improvement company for other organisations to become more sustainable and resilient and finally to inspire trust in their products, systems, services, and the world we live in.
Headquartered in London, BSI is the world's first national standards organization with more than 100 years of experience. We are a global partner for 86,000 companies and organizations in over 193 countries, offering development, auditing, certification, and training services, including innovative software solutions and cyber security expertise for all industries: from aerospace and automotive to food, construction, energy, healthcare, IT and trade sectors. Incorporated by Royal Charter, we're truly impartial, and home to the ultimate mark of trust, the Kitemark.
Through our unique combination of consulting, training, assurance and regulatory services we bring solid and broad knowledge to every company.
If you want to contribute to this inspiring challenge, bring your open and enthusiastic mindset to our dynamic team, apply now and become part of the BSI family!
D&I Policy
BSI is committed to ensuring the diversity of our workforce reflects that of our clients and the communities in which we operate.Our goal is to create a sense of belonging for all employees by providing opportunities to develop, grow, andengage with our global organization all while having fun doing great work.BSI is a community where everyone can thrive.
If you require any reasonable accommodations to be made on account of a disability orimpairment throughout out our recruiting process,please inform your Talent Acquisition Partner.
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About Us
BSI is a business improvement and standards company and for over a century BSI has been recognized for having a positive impact on organizations and society, building trust and enhancing lives.
Today BSI partners with more than 77,500 clients in 195 countries and engages with a 15,000 strong global community of experts, industry and consumer groups, organizations and governments.
Utilizing its extensive expertise in key industry sectors - including automotive, aerospace, built environment, food and retail, and healthcare - BSI delivers on its purpose by helping its clients fulfil theirs.
Living by our core values of Client-Centricity, Agility, and Collaboration, BSI provides organizations with the confidence to grow by partnering with them to tackle society's critical issues - from climate change to building trust in digital transformation and everything in between - to accelerate progress towards a better society and a sustainable world.
BSI is an Equal Opportunity Employer dedicated to fostering a diverse and inclusive workplace.