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Senior Manufacturing Engineer

Job in Eden Prairie, Hennepin County, Minnesota, 55344, USA
Listing for: Bracco Medical Technologies
Full Time position
Listed on 2026-02-28
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

We care as much about our employees as we do our patients. Our culture fosters a work environment where employees can thrive, be passionate and have fun along the way. Each member of the Bracco Medical Technologies team has the power to make a difference......every day!

The Senior Manufacturing Engineer is a hands-on technical lead with a primary focus on Operational Excellence & Manufacturing Support, followed by process development and manufacturing test. The role ensures stable, compliant, and efficient manufacturing of electro-mechanical medical devices. This role, which will provide an on-the-floor presence and strong cross-functional influence, will partner closely with Production, R&D, Quality, and Regulatory to resolve issues, optimize throughput, improve yield, and transfer robust processes and test systems into production.

Primary

Duties & Responsibilities
  • Serve as the first-line technical owner for assigned product lines and value streams, providing daily support for NC/MRB resolution, ECO/CO execution, rework development, design implementation, troubleshooting, and line balancing.
  • Lead structured problem-solving efforts (5-Why, Fishbone, Fault Tree) and drive CAPA completion with data-backed effectiveness verification (SPC, Cpk/Ppk, trend analysis).
  • Execute continuous improvement projects and initiatives—kaizen/A3 events, waste elimination, OEE/uptime improvement, cycle time reduction.
  • Update PFMEA, control plans, and risk documentation to maintain compliance with QMS requirements.
  • Design, fabricate/source, and document manufacturing fixtures, tooling, semi-automation solutions, and ergonomic workstations.
  • Partner with suppliers and contract manufacturers on process capability, qualifications, and change control.
  • Influence cross-functional decisions using data, structured problem solving, and clear communication.
  • Maintain a strong on-the-floor presence to support operators, troubleshoot issues, and ensure stable daily performance.
Process Development
  • Drive DFM/DFA and manufacturability considerations early in product development; shape part strategies, assembly flow, ergonomics, and automation opportunities.
  • Lead process and line concepting (layouts, takt modeling, throughput modeling), proof-of-principle builds, and DOE activities to establish robust process windows for CTQs.
  • Design, source, and document fixtures, tooling, semi-automation solutions, and ergonomic workstations.
  • Author and execute IQ/OQ/PQ protocols for processes, equipment, and fixtures, including sampling plans, statistical justification, and revalidation criteria.
  • Manage process transfer activities into production, including pilot builds, ramp-to-rate, FPY stabilization, and documentation readiness under Design Controls.
  • Mentor technicians and junior engineers in ME fundamentals and best practices.
Manufacturing Test (New & Legacy technologies)
  • Develop new manufacturing test fixtures and systems for new products in close partnership with R&D. R&D owns test requirements and early prototypes; the Manufacturing Engineer converts these into robust, production-ready solutions.
  • Improve, upgrade and modernize legacy testers by refining hardware, software, instrumentation, and data collection approaches to reduce variation, improve uptime, and enhance diagnostic capability.
  • Lead TMV/MSA efforts (Gage R&R, correlation, linearity, repeatability) for both new and legacy systems to ensure accurate, reliable measurement performance.
  • Perform periodic tester verification checks, trend performance data, and drive corrective actions to maintain validated state and ensure long-term stability.
  • Author and execute IQ/OQ/PQ protocols for new and updated test fixtures and systems, providing clear, audit-ready documentation aligned with ISO 13485 and FDA expectations.
Qualifications (Knowledge, Skills & Abilities):

Minimum

  • BS in Manufacturing, Mechanical, Industrial Engineering, or related field.
  • Minimum of 5 years of experience in a regulated manufacturing environment; medical device strongly preferred.
  • Strong background in production support, troubleshooting, and maintaining validated manufacturing processes.
  • Demonstrated expertise in IQ/OQ/PQ, DFM/DFA, DOE,…
Position Requirements
10+ Years work experience
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