
Senior Principal Quality Engineer
- Lafayette, CO
- Permanent
- Full-time
- Supplier selection and qualification while ensuring suppliers deliver quality parts, materials, and services.
- Monitor parts from acquisition through the manufacturing cycle, promptly identifying and resolving supplier-related problems.
- Experience with PCBA suppliers and validation of PCBA test and manufacturing processes strongly preferred.
- Develop and prioritize an auditing schedule to ensure suppliers meet GMP and quality standards through regular audits.
- Evaluate suppliers' internal functions to assess overall performance and provide feedback.
- Manage Non-Conformance Material Reports (NCMRs) on materials-related quality issues and trends (Incoming, Production, Sterilization).
- Handle suppliers' change requests, including communication, project management via MAP Agile workflow, and regular reporting.
- Manage the Approved Supplier List, including administrative work in MAP Agile.
- Qualify materials through the Production Part Approval Process (PPAP), including process validation, test method validation, technical writing, and project management.
- Improve suppliers' performance and reduce escapes to manufacturing.
- Execute Process validation IQ/OQ/PQ and Master Validation Planning in new product development.
- Knowledgeable in Statistical analysis (MSA, Capability, SPC)
- Support DFMEA and PFMEA activities
- Identification of critical to quality parameters and process controls in collaboration with designers and cross-functional team
- Design Transfer; translating design specifications into production specifications.
- Use project management skills to ensure that supplier processes are developing at the appropriate cadence to support engineering builds and Design Verification and Validation.
- Provide mentorship and coaching.
- The job requires occasional travel to visit suppliers within the United States and internationally.
- Bachelor’s degree in engineering or related field
- Minimum of 10 years of relevant experience, or advanced degree with a minimum of 8 years relevant experience
- Experience with PCBA suppliers and validation of PCBA test and manufacturing processes strongly preferred
- Medical device manufacturing industry experience, preferably ISO 13485.
- Lead auditor experience.
- Hands-on experience with SAP, Trackwise, Agile change management.
- Ability to manage tasks and projects under tight deadlines with a sense of urgency.
- Strong communication and presentation skills, with the ability to confidently address external audiences and high-level leadership.
- Comfortable navigating through complex networks with diplomatic approaches and reporting to a flattened organization.
- Equipped with sophisticated problem-solving methodologies (Lean/Sigma) and great attention to detail to fit for fast-accurate action-driven environments.
- Engage in changes and advocate for inclusion/diversity.
- Experience with materials and manufacturing processes such as PCBAs, MIM, nitinol, cables, crimping, laser welding, automated functional testing
- DRM or DFSS
- Knowledge of GD&T
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):$147,200.00 - $220,800.00This 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:About MedtronicWe 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 95,000+ 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 .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 find 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.