Principal Manufacturing Engineer

We anticipate the application window for this opening will close on 31 Dec 2026.

Principal Manufacturing Engineer for Medtronic, Inc. in Jacksonville, FL. Responsible for coordinating and executing the Medtronic site Verification and Validation (V&V) deliverables, for supplier transfers within the Supplier Optimization group (Transfer Office) under the Operations Innovation team. Assist with defining Quality Impact Level (QIL) of supplier qualified product. Design assembly and holding fixtures, coordinate supplier fabrication, and develop protocols, reports, process instructions, preventive maintenance plans, and calibration schedules.

Navigate the complexities of various government and industry regulations to include FDA 21 CFR part 820, European Union Medical Device Regulation (EU MDR), ISO 13485, ISO 14971, and Good Manufacturing Practices (GMP). Responsible for the PPAP (Production Part Approval Process) for supplier provided goods. Leverage IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification). Utilize Minitab and associated statistical tools including TMV (Test Method Validation), Capability (Ppk / Tolerance Intervals), and SPC (Statistical Process Control).

Responsible for providing Control Plans, Process Flow Maps, and PFMEA (Process Failure Mode and Effects Analysis). Coordinate the creation and approval of V&V protocols / reports to include top-level assembly or sub-assembly test acceptance criteria, sample sizes based on component/feature criticality, and sampling plans. Leverage AGILE, SAP, and ERP system knowledge based on Medtronic Operating Unit/site requirements. Execute First Article Inspection activities and summation of results.

Update all BOM (Bill of Material) structure within the appropriate QMS (Quality Mgmt. System). Relocation assistance is not available for this position. #LI-DNI.

Masters’ Degree in Mechanical, Industrial, or Biomedical Engineering or related engineering field and five (5) years of experience as a manufacturing or design engineer for medical devices, or, Bachelors’ Degree in Mechanical, Industrial, or Biomedical Engineering or related engineering field and seven (7) years of experience as a manufacturing or design engineer for medical devices. Must possess at least five (5) years’ experience with each of the following: FDA 21 CFR part 820, EU MDR, ISO 13485, ISO 14971, and GMP;

PPAP and IQ/OQ/PQ;
Minitab, TMV, Capability (Ppk / Tolerance Intervals), and SPC;
Control Plan, Process Flow Map, and PFMEA;
Creation and approval of V&V protocols, reports for top-level assembly and sub-assembly test acceptance criteria, sample sizes based on component/feature criticality, and sampling plans; AGILE, SAP, and ERP systems;
Executing First Article Inspection activities and summation of results; and Updating BOM structure within QMS.

Salary: $144,000 to $184,800 per year

• 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
• Simple Steps (global well-being program)

• 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)
• 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…