Medical Device Product Development Lifecycle Neuroscience, Surgical navigation, and or Cranial Spinal Technologies For Baccalaureate degrees earned outside of the United States, a degree that ...
New
Medical Device Product Development Lifecycle Neuroscience, Surgical navigation, and or Cranial Spinal Technologies For Baccalaureate degrees earned outside of the United States, a degree that ...
New
Medical Device Product Development Lifecycle Neuroscience, Surgical navigation, and or Cranial Spinal Technologies For Baccalaureate degrees earned outside of the United States, a degree that ...
New
Medical Device Product Development Lifecycle Neuroscience, Surgical navigation, and or Cranial Spinal Technologies For Baccalaureate degrees earned outside of the United States, a degree that ...
New
Medical Device Product Development Lifecycle Neuroscience, Surgical navigation, and or Cranial Spinal Technologies For Baccalaureate degrees earned outside of the United States, a degree that ...
New
Medical Device Product Development Lifecycle Neuroscience, Surgical navigation, and or Cranial Spinal Technologies For Baccalaureate degrees earned outside of the United States, a degree that ...
New
Medical Device Product Development Lifecycle Neuroscience, Surgical navigation, and or Cranial Spinal Technologies For Baccalaureate degrees earned outside of the United States, a degree that ...
New
Leads the planning of new product development projects using structured phase-gate and design control processes common to the medical device industry. Develops andmaintainsdetailed Gantt charts ...
Leads the planning of new product development projects using structured phase-gate and design control processes common to the medical device industry. Develops andmaintainsdetailed Gantt charts ...
Principal Duties and Responsibilities: • Leads the planning of new product development projects using structured phase-gate and design control processes common to the medical device industry. • ...
Principal Duties and Responsibilities: • Leads the planning of new product development projects using structured phase-gate and design control processes common to the medical device industry. • ...
Prior experience in medical device development required. * Prior experience in taking a medical device or similar product from ideation to commercialization required. * Ability to read and interpret ...
Prior experience in medical device development required. * Prior experience in taking a medical device or similar product from ideation to commercialization required. * Ability to read and interpret ...
$19.50 - $21/hr
Ability to learn advanced assembly skills and product flow process * Ability to reliably interpret ... medical devices. We hire individuals who are looking for more than just a job. Every role at our ...
$19.50 - $21/hr
Ability to learn advanced assembly skills and product flow process * Ability to reliably interpret ... medical devices. We hire individuals who are looking for more than just a job. Every role at our ...
Denver, CO · On-site
$130K - $171K/yr
Requisition ID: 65189 Title: Sr. Product Manager, Vet Systems Arthrex, Inc. is a global medical device company and a leader in new product development and medical education within the orthopedic ...
Denver, CO · On-site
$130K - $171K/yr
Requisition ID: 65189 Title: Sr. Product Manager, Vet Systems Arthrex, Inc. is a global medical device company and a leader in new product development and medical education within the orthopedic ...
Arvada, CO · On-site
$19.50 - $21/hr
Ability to learn advanced assembly skills and product flow process * Ability to reliably interpret ... medical devices. We hire individuals who are looking for more than just a job. Every role at our ...
Arvada, CO · On-site
$19.50 - $21/hr
Ability to learn advanced assembly skills and product flow process * Ability to reliably interpret ... medical devices. We hire individuals who are looking for more than just a job. Every role at our ...
Develop and implement comprehensive global regulatory strategies for medical device submissions to ensure timely market access for New Product Development * Author regulatory submissions, including ...
Develop and implement comprehensive global regulatory strategies for medical device submissions to ensure timely market access for New Product Development * Author regulatory submissions, including ...
Develop and implement comprehensive global regulatory strategies for medical device submissions to ensure timely market access for New Product Development * Author regulatory submissions, including ...
Develop and implement comprehensive global regulatory strategies for medical device submissions to ensure timely market access for New Product Development * Author regulatory submissions, including ...
Develop and implement comprehensive global regulatory strategies for medical device submissions to ensure timely market access for New Product Development * Author regulatory submissions, including ...
Develop and implement comprehensive global regulatory strategies for medical device submissions to ensure timely market access for New Product Development * Author regulatory submissions, including ...
The Product Development Engineer II is responsible for leading new product development activities ... in the medical device. * Experience in high volume manufacturing and assembly processes ...
The Product Development Engineer II is responsible for leading new product development activities ... in the medical device. * Experience in high volume manufacturing and assembly processes ...
The Product Development Engineer II is responsible for leading new product development activities ... in the medical device. * Experience in high volume manufacturing and assembly processes ...
The Product Development Engineer II is responsible for leading new product development activities ... in the medical device. * Experience in high volume manufacturing and assembly processes ...
Golden, CO · On-site
$100 - $145/hr
... medical device environment. This role serves as the central point of accountability for program ... Lead operational readiness reviews and production hand‑off activities from development to ...
Golden, CO · On-site
$100 - $145/hr
... medical device environment. This role serves as the central point of accountability for program ... Lead operational readiness reviews and production hand‑off activities from development to ...
... medical device environment. This role serves as the central point of accountability for program ... Lead operational readiness reviews and production hand-off activities from development to ...
... medical device environment. This role serves as the central point of accountability for program ... Lead operational readiness reviews and production hand-off activities from development to ...
Golden, CO · On-site
$100K - $145K/yr
... medical device environment. This role serves as the central point of accountability for program ... Lead operational readiness reviews and production hand-off activities from development to ...
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Golden, CO · On-site
$100K - $145K/yr
... medical device environment. This role serves as the central point of accountability for program ... Lead operational readiness reviews and production hand-off activities from development to ...
Golden, CO · On-site
$100 - $145/hr
... medical device environment. This role serves as the central point of accountability for program ... Lead operational readiness reviews and production hand‑off activities from development to ...
Golden, CO · On-site
$100 - $145/hr
... medical device environment. This role serves as the central point of accountability for program ... Lead operational readiness reviews and production hand‑off activities from development to ...
... medical device environment. This role serves as the central point of accountability for program ... Lead operational readiness reviews and production hand-off activities from development to ...
... medical device environment. This role serves as the central point of accountability for program ... Lead operational readiness reviews and production hand-off activities from development to ...
... preferably medical device) product development or testing environment. Knowledgeable and experience in software and hardware development and the processes associated with product life-cycles.
... preferably medical device) product development or testing environment. Knowledgeable and experience in software and hardware development and the processes associated with product life-cycles.
$44.7K - $54.4K
1% of jobs
$54.4K - $64.2K
0% of jobs
$64.2K - $73.9K
2% of jobs
$73.9K - $83.7K
3% of jobs
$83.7K - $93.4K
4% of jobs
$93.4K - $103.2K
4% of jobs
$103.2K - $112.9K
4% of jobs
$119.6K is the 25th percentile. Wages below this are outliers.
$112.9K - $122.7K
9% of jobs
$122.7K - $132.4K
6% of jobs
$132.4K - $142.2K
2% of jobs
The median wage is $144.3K / yr.
$142.2K - $151.9K
64% of jobs
$44.7K
$133.5K
$151.9K
A Medical Device Product Development job involves designing, testing, and bringing medical devices to market while ensuring compliance with regulatory standards. Professionals in this role work with cross-functional teams, including engineering, regulatory affairs, and manufacturing, to develop safe and effective healthcare solutions. They oversee the entire product lifecycle, from concept and prototyping to clinical validation and commercialization. Strong knowledge of FDA, ISO, and other regulatory requirements is essential.
Professionals in Medical Device Product Development often encounter challenges such as navigating complex regulatory requirements, managing cross-functional project teams, and ensuring that products meet both clinical needs and quality standards. Balancing innovative design with safety and compliance can require careful planning and solid problem-solving skills. Additionally, adapting to shifting project timelines and incorporating stakeholder feedback are common aspects of the job. Overcoming these challenges is rewarding and helps ensure the delivery of safe, effective devices to patients and healthcare providers.
To thrive in Medical Device Product Development, you need a strong background in engineering or life sciences, product design, and an understanding of regulatory requirements like FDA and ISO standards. Proficiency with CAD software, project management tools, and knowledge of quality management systems (QMS) is commonly required, along with certifications such as Six Sigma or PMP being beneficial. Strong problem-solving abilities, collaboration skills, and effective communication are key soft skills for this role. These skills are important to ensure that devices are developed safely, efficiently, and in compliance with industry regulations while fostering innovation and teamwork.

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted yesterday
New
7.9
Based on 176 frontline employees who took The Breakroom Quiz
161st of 538 rated manufacturers
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
A Day in the LifeResponsibilities may include the following and other duties may be assigned.
TECHNICAL SPECIALIST CAREER STREAM:An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies. Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering R&D, systems or initiatives related to new technologies or therapies - from design to implementation - while adhering to policies, using specialized knowledge and skills.
DIFFERENTIATING FACTORS
Autonomy:Established and productive individual contributor.
Works independently with general supervision on larger, moderately complex projects / assignments.
Organizational Impact:Sets objectives for own job area to meet the objectives of projects and assignments.
Contributes to the completion of project milestones.
May have some involvement in cross functional assignments.
Innovation and Complexity:Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex.
Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area.
Communication and Influence:Communicates primarily and frequently with internal contacts.
External interactions are less complex or problem solving in nature.
Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision-making.
Leadership and Talent Management:May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream.
Required Knowledge and Experience: Requires a Baccalaureate degreeand minimum of 2 years of relevant experience OR Master's degree with a minimum of 0 years relevant experience.
Preferred Knowledge and Experience:
Medical Device Product Development Lifecycle
Neuroscience, Surgical navigation, and or Cranial Spinal Technologies
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Recruitment Fraud Alert
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.
Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance,Health Savings Account,Healthcare Flexible Spending Account,Life insurance, Long-term disability leave,Dependent daycare spending account,Tuition assistance/reimbursement, andSimple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees:Incentive plans, 401(k) plan plus employer contribution and match,Short-term disability,Paid time off,Paid holidays,Employee Stock Purchase Plan,Employee Assistance Program,Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), andCapital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
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