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Medtronic

Senior Sourcing Engineer

Reposted Yesterday
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In-Office
Lafayette, CO
113K-156K Annually
Mid level
In-Office
Lafayette, CO
113K-156K Annually
Mid level
The role involves technical liaison between design requirements and suppliers, ensuring compliance with medical device standards, and driving continuous improvement projects.
The summary above was generated by AI
We anticipate the application window for this opening will close on - 25 Sep 2025

Position Description:       

Sr. Sourcing Engineer for Covidien, LP (a Medtronic company) located in Lafayette, CO. Provide technical engineering expertise and serve as the technical liaison between Medtronic design requirements and suppliers' technical capability to support business objectives; facilitate Lean-Sigma continuous improvement with suppliers, support and implementation; identify risks associated with low margins between supplier processes and design requirements; understand and conform with medical device industry standards and regulatory requirements to include Food and Drug Administration (FDA) regulations, ISO 13485, ISO 14971, 21 CFR Part 820, IEC 60601, Corrective Action & Preventive Action (CAPA), and GMP (Good Manufacturing Practices); execute lean transformation projects, product transfers, cost savings and material replacement projects with suppliers; coordinate and drive continuous improvement activities including process characterizations and optimization using methodologies including Design of Experiments (DOE), Time studies, value analysis and value engineering (VAVE), DRM (Design, Reliability and Manufacturability), and Lean Six Sigma; facilitate selection of new suppliers ensuring Medtronic design requirements are met; coordinate root cause investigations of product or process non-conformances using six sigma methodology; establish process flows, coordinate process validations using Installation Qualification, Operational Qualification and Performance Qualification (IQ/OQ/PQ) protocols; oversee statistical analysis by using techniques including Gage R and R, ANOVA, variables data distribution, sample size calculation, statistical process control, and Capability and Normality Assessments; oversee and coordinate Critical Feature Identification (CFI), Critical to Quality (CTQ) determination, Process Failure Mode and Effect Analysis (PFMEA), and Design Failure Mode and Effect Analysis (DFMEA) activities; and coordinate inspection methods including variables and attribute.

Position works a hybrid model and will be onsite in Lafayette, CO – 4 days per week.

Basic Qualifications:        

Bachelors’ Degree in Electrical, Mechanical or Biomedical Engineering or related engineering field and four (4) years as a supplier, electrical or quality engineer or related occupation in supplier quality engineering for medical devices. Must possess at least four (4) years’ experience with each of the following: FDA regulations, 21 CFR Part 820, ISO 13485, ISO 14971, IEC 60601, CAPA, and GMP; Lean transformation projects, product transfers, cost savings and material replacement projects; Process characterizations and optimization using methodologies including DOE, Time studies, VAVE, and Lean Six Sigma; Identifying root cause of product or process non-conformances; Establishing process flows and conducting process validations using IQ/OQ/PQ; Gage R &R, ANOVA, variables data distribution, sample size calculation, statistical process control, and Normality Assessments; CFI, PFMEA, DFMEA, and CTQ; Coordinating inspection methods including variables and attribute.

Salary:  $113,400 to $156,000 per year

#LI-DNI

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

Top Skills

21 Cfr Part 820
Capability And Normality Assessments
Design Of Experiments (Doe)
Fda Regulations
Iec 60601
Iso 13485
Iso 14971
Lean Six Sigma
Statistical Analysis

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