Senior Design Quality Engineer - San Diego, CA (Onsite)
Senior Design Quality Engineer - San Diego, CA (Onsite)
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
$ 96800 - 145200
1 Vacancy
Job Description
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.
A Day in the Life
Careers that Change Lives
We are currently looking for a Senior Design Quality Engineer to join our Cranial and Spinal Technologies (CST) operating unit. CST provides a comprehensive portfolio of proven powerful technologies setting the highest standards of integrity and reliability in Cranial and Spinal care.
This position is located ONSITE in San Diego CA collaborating with team in Memphis TN.
In this exciting role you will have primary responsibility for developing and coordinating quality assurance activities working in a cross functional team setting. This is a dynamic opportunity where you will also be involved in leading production control and execution on projects of strategic importance.
Responsibilities may include the following and other duties may be assigned.
Perform duties as the technical liaison between contract manufacturers and Medtronic site(s) - devise and implement methods/ procedures for inspecting testing and evaluating the precision accuracy stability and control of products and/ or production equipment.
Collaborate with internal and contract manufacturing engineering teams to ensure purchased products and/ or components are manufactured and qualified in accordance with applicable industry standards and regulatory requirements.
Develop and maintain quality records per established processes - design history files risk management change requests across the product lifecycle.
Monitor parts through the development and production value stream communicate and resolve issues in a timely manner (including leading nonconformance assessments investigations corrective and preventive actions)
Partner with global functions and contract manufacturers to ensure designated suppliers are monitored on a regular basis (via audits onsite reviews continuous improvement initiatives etc) for ensuring continued adherence to good manufacturing practices (GMP) and quality standards are met.
May specialize in the areas of design incoming material production control product evaluation and reliability inventory control and/or research and development as they apply to product or process quality.
Must Have: Minimum Qualifications
To be considered for this role please ensure the minimum requirements are evident on your resume.
Bachelors Degree in a technical discipline
Minimum of 4 years of relevant experience or advanced degree with a minimum of 2 years relevant experience.
Nice to Have: Preferred Qualifications
Experience working with global engineering teams in the medical device industry.
Ability to work effectively in a team environment and build strong working relationships.
ASQ Quality certification CQE CSQP CQA.
Hands on experience with metrology statistical tools and supplier controls
Experience with international standards for development production control and Quality Management Systems
Lean Six Sigma Green Belt or Black Belt.
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.
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
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 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 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.
Required Experience:
Senior IC
Employment Type
Full-Time
