At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.
Responsibilities may include the following and other duties may be assigned.
Lead the electrical design and development of advanced electrochemical glucose sensor systems including circuitry embedded systems and signal processing algorithms.
Define and execute verification and validation strategies for sensor electronics ensuring compliance with relevant medical device standards (ISO 13485 IEC 60601 etc.).
Drive innovation through the evaluation and adoption of new materials sensor architectures and low-power electronics.
Oversee design documentation risk analysis and failure mode analysis (FMEA) for sensor-related components.
Interface with external partners suppliers and research organizations to advance sensor technology.
Present technical findings and project updates to executive leadership and cross-functional stakeholders.
Architect electrical systems for continuous glucose monitors or other diagnostic platforms
Develop signal conditioning circuits analog front ends and data acquisition systems for biosensor applications
Design low-noise high-precision potentiostat circuits and amperometric measurement systems
Develop algorithms for signal processing noise reduction and biomarker detection
Create electrical interfaces between biosensors and embedded systems
Optimize sensor performance parameters including sensitivity selectivity and stability
Drive innovation in sensor miniaturization power optimization and wireless connectivity
Collaborate with chemistry mechanical software systems and manufacturing teams to integrate sensor technology into commercial diabetes devices.
Mentor and guide junior engineers and project teams in design best practices troubleshooting and root cause analysis.
Review and approve electrical designs test protocols and validation procedures
Lead design reviews and risk analysis activities
Ensure designs comply with FDA regulations (21 CFR Part 820) IEC 60601 and ISO 13485
Support regulatory submissions including 510(k) and PMA applications
Implement design controls and verification/validation protocols per medical device standards
Partner with regulatory and quality teams to support submissions audits and compliance activities.
Required Knowledge and Experience:
Requires a Bachelors degreeand minimum of 10 years of relevant experience OR Masters degree with a minimum of 8 years relevant experience OR PhD with 6 years relevant experience.
Nice to Have:
MS or PhD Degree in Electrical Engineering or Applied Physics
5 years of hands-on experience with electrochemical biosensing systems
Deep understanding of electrochemical principles (cyclic voltammetry impedance spectroscopy potentiometry)
Proven experience designing potentiostat circuits and electrochemical instrumentation
Proficiency in analog circuit design mixed-signal systems and low-power electronics
Experience with biosensor fabrication techniques and electrode materials
Knowledge of biocompatibility requirements and sensor packaging for biological environments
Strong background in signal processing and data analysis for biosensor applications
Experience with wireless communication protocols (Bluetooth NFC) for medical devices
Proficiency in circuit simulation tools (SPICE Cadence) and PCB design (Altium )
Deep knowledge of PCBA design and manufacturing processes
Understanding of medical device regulations and quality systems
Excellent leadership communication problem-solving and analytical skills
Experience with design for manufacturability reliability and testability in a regulated environment.
MS or PhD in Electrical Engineering Biomedical Engineering or related field
Previous experience with continuous glucose monitoring or other implantable sensors
Knowledge of machine learning applications in biosensor data analysis
Experience with ISO 14971 risk management processes
Publication record in peer-reviewed journals related to biosensing
Experience leading cross-functional teams in regulated environments
Hands-on experience with microfabrication MEMS or biosensor integration.
Knowledge of diabetes care products and user needs.
Proficiency with simulation and modeling tools (e.g. SPICE MATLAB).
Track record of patents publications or contributions to industry standards.
Knowledge of manufacturing test equipment design
Experience working with vendors and contract manufacturers for PCB fabrication and assembly
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.
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.
The following benefits and additional compensation are available to those regular employees who work 20 hours per week: Health Dental and vision insuranceHealth Savings AccountHealthcare Flexible Spending AccountLife insurance Long-term disability leaveDependent daycare spending accountTuition 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 matchShort-term disabilityPaid time offPaid holidaysEmployee Stock Purchase PlanEmployee Assistance ProgramNon-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
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 95000 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 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.
Required Experience:
Staff IC
About Medtronic Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an excit ... View more