We anticipate the application window for this opening will close on - 7 Jan 2025

 

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

Team is working hybrid and position will be onsite 2 days/week in Carlsbad, CA.

At our Design Quality Engineering department in Medtronic we focus on providing Engineering support for Design and Development, Quality Compliance, and Risk Management activities across the Ventilation Service Solutions portfolio. As a Senior Design Quality Engineer, you will apply Design Controls and Risk Management principles to ensure that any changes to our sustaining ventilation products are safe, effective, and compliant to associated Regulations and Methods.  You will join a team of four engineers in a senior role.

Come for a job, stay for a career!

Responsibilities may include the following and other duties may be assigned:

•    Responsible for ensuring that mechanical, electrical, software, and labeling changes to existing products (ventilators and accessories)  are conducted in compliance with the FDA Quality System Regulations and EU MDR requirements. This position will focus on software design changes.
•    Responsible for approving product requirements and modified product designs for quality characteristics, including reliability, maintainability, serviceability, and testability.
•    Participate on cross-functional teams to maintain Product Risk Management Files (Risk Management Plan, Risk Assessments, DFMEA and Risk Management Report) and facilitate Post Launch Risk Management Reviews.
•    Participate in Post-Market Surveillance and signal detection activities. Provide Quality support to facilitate the rapid resolution of Product Complaints and/or Patient Safety issues. Author Issue Impact Assessments (IIA/HHE).
•    Participate in the development of Design Verification and Validation Test Plans / Protocols and provide guidance on Standards compliance. 
•    Challenge proposals during Formal Technical Design Reviews. 
•    Provide guidance and direction for sample size and test method validation.
•    Provide guidance to project teams on all Quality Policies / Procedures (including verification, validation, statistical methods, risk management, and design controls).
•    Review Design History Files and EU MRD files for conformance to applicable requirements and support occasional Regulatory Affairs activities.  
•    Participate in the CAPA process.
•    Provide assistance during Compliance audits.

Must Have: Minimum Requirements

•    Bachelor's degree plus 4+ years of quality or engineering experience (or 2+ years with an advanced degree)

Nice to Have

•    Bachelor’s Degree in Engineering, Physics, Science fields, or Math  
•    5+ years industry experience Quality Assurance, R&D, or Regulatory Affairs in  Medical Device or Pharmaceutical Industries.
•    Experience with Medical Device Quality Systems (21 CFR 820, ISO-13485, and EU MDR)
•    Strong familiarity with ISO-14971 and IEC-62304
•    Excellent written and verbal communication skills
•    Proficiency with MS Office, Outlook, PowerPoint, and Teams
•    Experience with biocompatibility standards requirements verification is desirable
•    Experience with Li-ion batteries

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.

Benefits & Compensation
 

Medtronic 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.
 

Salary ranges for U.S (excl. PR) locations (USD):$98,400.00 - $147,600.00

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

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, and Simple 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), and Capital 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

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 90,000+ passionate people. 
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Learn more about our business, mission, and our commitment to diversity here.

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.