Careers That Change Lives

　　As a member of the Medtronic Diabetes – Continuous Glucose Monitoring Sensor R&D team the Sr. Process Engineer will support the development of next generation CGM products. This position will play a key role in the development of various new/improved chemistry layers/coatings of glucose sensors by designing and executing design feasibility, process development, and manufacturing transfer. This role will be responsible for driving the product build documentation, design and executing experiments and builds of sensors for pilot scale evaluations, execute data trending & statistical analysis. Upon successful process and design optimization, this role will subsequently support tech transfer to new product introduction and manufacturing teams. You will manage deliverables for multiple projects and maintain an effective system for tracking progress. You will be interfacing with Managers, Engineers &Technicians in R&D and New Product Introduction (NPI) Operations teams as well as Quality and Clinical groups to accomplish day to day activities. The candidate must have strong organizational skills, attention to details, an analytical mindset and ability to communicate effectively with multiple stakeholders.

　　Engineers create our market-leading portfolio of innovations. Join us to make a lasting impact. Help bring the next generation of life-changing medical technology to patients worldwide.

　　A Day in the Life

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

　　Develop & utilize technical & wet lab skills associated with medical device coatings/deposition & relevant fabrication processes

　　Utilize design of experiments (DOEs), statistical process control, and statistical data analysis methodologies in developing new designs and processes to integrate with next generation sensors

　　Generate documentation following good documentation practices in relation to product builds & instructions, clinical documentation, specifications, etc. and drive approvals

　　Act as a key interface with Manufacturing/Production teams

　　Coordinate with material inventory and external or internal vendors in sourcing raw materials and parts for the prototype builds

　　Develop and support Bill Of Materials (BOM)

　　Oversee & coordinate device build, sterilization, and testing

　　Resolve non-compliance issues and inefficiency issues, recommending and implementing process changes.

　　Provides technical support to device failure analysis on devices

　　Attend prototype product build coordination meetings, including schedule management; gather and verify requirements and communicate updates to stakeholders in a timely manner

　　Utilize knowledge of project management, schedules and deliver on day-to-day tasks to accomplish goals for a specific project

　　Must Have: Minimum Requirements

　　To be considered for this role, please ensure the minimum requirements are evident in your applicant profile.

　　Bachelors Degree in Engineering, Chemistry, or Physics and 4+ years product or process development

　　OR

　　Masters Degree in Engineering, Chemistry, or Physics and 2+ years product or process development

　　Nice to Have

　　Prior experience with coatings/deposition methodologies including spray, slot, spin, CVD, PVD, as relevant to medical device or semiconductor industries (ex: MEMS photolithography processes)

　　Standard wet lab techniques as applicable to chemistry or biology labs

　　Prior experience working in a manufacturing or prototype line in a cleanroom environment in medical device, pharmaceutical or semiconductor industry

　　Experience with statistical data analysis software (Ex. Minitab, JMP, etc.) and standard statistical tests (T-test, ANOVA)

　　Experience in programming with MATLAB and/or Python

　　Performed R&R studies, demonstrating process capability (Ppk & Cpk), and Qualification procedures (IQ/OQ/PQ)

　　Exposure to Design for Reliability and Manufacturability (DRM) principles and/or process and performance improvement tools such as Lean and/or Six Sigma

　　Experience with technical documentation (Work Instructions, laboratory notebooks, publications, engineering reports, change requests, IQ/OQ/PQ’s, Standard Operating Procedures, test protocols, BOMs, DHFs etc.)

　　Exposure to inventory management and ordering systems (e.g. SAP)

　　Prior project management experience

　　Ability to collaborate with multiple departments to analyze and assess Non-conformances and mitigate risk by following established procedures.

　　Demonstrated written and verbal communication skills

　　Ability to manage multiple tasks & projects and work independently & within a team-based environment

　　Experience with quality documentation and systems (e.g. Agile PLM.)

　　About Medtronic

　　Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services 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 exciting and rewarding place to be.

　　We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.

　　Physical Job Requirements

　　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. (ADA-United States of America)

　　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. Learn more about our benefits here (https://www3.benefitsolver.com/benefits/BenefitSolverView?page_name=signon&co_num=30601&co_affid=medtronic) .

　　This position is eligible for a short-term incentive plan.  Learn more about Medtronic Incentive Plan (MIP) on page 6 here .

　　The provided base salary range is used nationally (except in certain CA locations). The rate offered is compliant with federal/local regulations and may vary by experience, certification/education, market conditions, location, etc.   

　　Min Salary

　　92000

　　Max Salary

　　138000

　　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.