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Senior Electrical Manufacturing Engineer

MiniMed · Northridge, CA

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Level
Senior
Team
Reliability
Base pay
$87k–$149k
Degree
Required
Experience asked
4+ years
Certification
Black Belt preferred
Industry
Medical devices
Posted
4 days ago

The role in 30 seconds

A senior reliability role at MiniMed (medical devices) in Northridge, CA. Evaluate, qualify, and implement new materials, equipment, and technologies to improve process performance and competitiveness.

They ask for
4+ years · degree required · Black Belt preferred
Tools it names
Lean, Six Sigma, Kaizen, Value stream mapping, Root cause, SPC
Base pay
$87k–$149k

Read from the posting. The full description is below.

How this role compares

Against 89 other live reliability postings in California.

Base pay
About 13% below similar roles

Typical $111k–$160k, from 50 postings that list pay.

Experience asked
Less than usual (4+ vs 5+)

Similar roles usually ask 5+ years.

Skills these teams ask for most

  • ✓ Root cause 79%
  • ✓ FMEA 50%
  • ✓ New product launch 49%
  • ✓ Automation 39%
  • ✓ DOE 29%
  • ✓ SPC 24%

✓ = this posting asks for it too. % = share of similar postings that mention it.

Stands out: this posting asks for Kaizen, Value stream mapping, CAPA, ISO 13485, which few similar roles mention. If you have it, lead with it.

It asks for 4+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone on the team first.

At a glance

Training program

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Reliability team at MiniMed

    Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • The posting mentions a Black Belt. Does the company sponsor certification?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: MiniMed in Northridge

7 other open roles at this site.

All 8 roles at MiniMed →
Full description from MiniMedAs posted on their careers site.Show

About the Role

We are seeking an experienced and highly skilled Senior Electrical Manufacturing Engineer to lead and drive the development, optimization, and sustaining of complex PCBA manufacturing processes within a highly regulated medical device environment. This senior-level role requires deep technical expertise, strong leadership capabilities, and a proven track record of delivering high-quality PCBA solutions for life-critical medical products.

The ideal candidate will serve as a technical subject matter expert (SME), driving continuous improvement initiatives, leading cross-functional teams, and ensuring that all PCBA processes meet the most stringent quality, reliability, and regulatory standards in the medical device industry.

Responsibilities

may include the following and other duties may be assigned.

requirements

  • ✓Represent manufacturing engineering in cross-functional core teams and program reviews

requirements

  • ✓Lead CAPA investigations and drive systemic corrective actions for PCBA-related non-conformances and customer complaints
  • ✓Own process-level risk management activities in accordance with ISO 14971
  • ✓Ensure compliance with FDA 21 CFR Part 820, ISO 13485, IEC 60601 , and other applicable standards
  • ✓Support regulatory submissions, internal audits, and external inspections (FDA, Notified Body) related to PCBA manufacturing
  • ✓Drive implementation of Statistical Process Control (SPC) and key process indicators (KPIs) to monitor and control PCBA process performance

requirements

and collaborate with supply chain to resolve supplier-related PCBA issues

  • ✓Evaluate and approve material and component changes from a manufacturing process perspective

Required Qualifications

Requires a bachelor's degree and minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years of relevant experience.

Preferred Qualifications

  • ✓8–12+ years of progressive experience in PCBA manufacturing engineering
  • ✓5 years of experience in a regulated medical device, aerospace, or defense manufacturing environment
  • ✓Demonstrated experience leading NPI programs and complex process validation activities
  • ✓Technical Skills - SMT & Through-Hole Assembly Processes
  • ✓Expert - IPC Standards (IPC-A-610, J-STD-001)
  • ✓Expert - Reflow, Wave & Selective Soldering
  • ✓Expert - AOI, X-Ray & SPI Inspection Systems
  • ✓Expert - DFM / DFA Principles & Application
  • ✓Expert - IQ/OQ/PQ Process Validation
  • ✓Expert - FDA 21 CFR Part 820 / ISO 13485
  • ✓Expert - FMEA & Risk Management (ISO 14971)
  • ✓Expert - Root Cause Analysis (8D, 5-Why, DOE)
  • ✓Expert - Statistical Process Control (SPC)
  • ✓Expert - Conformal Coating & Cleaning Pr
Show full description ↓

At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down barriers to innovation for a more connected, compassionate world.

Advanced Process Engineering & Development

  • •Lead the design, development, validation, and continuous improvement of complex PCBA manufacturing processes including SMT, through-hole, reflow soldering, wave soldering, selective soldering, and advanced cleaning processes
  • •Drive process capability improvements using statistical methods and advanced engineering techniques to achieve best-in-class yields and quality metrics
  • •Own and lead full process qualification and validation (IQ/OQ/PQ) activities from planning through execution and approval
  • •Develop and implement Design for Manufacturability (DFM) and Design for Assembly (DFA) guidelines and ensure adoption by design engineering teams
  • •Lead advanced root cause analysis for complex, recurring, or high-impact PCBA manufacturing failures
  • •Evaluate, qualify, and implement new materials, equipment, and technologies to improve process performance and competitiveness
  • •Define and own process control plans, FMEAs, and control strategies for critical PCBA processes

New Product Introduction (NPI) Leadership

  • •Serve as the primary PCBA manufacturing engineering lead for NPI programs, from concept through full production transfer
  • •Lead manufacturing readiness reviews and ensure all PCBA processes are production-ready prior to launch
  • •Collaborate with R&D and design engineering teams during early-stage development to influence PCB layout, component selection, and assembly design decisions
  • •Define pilot build strategies, process qualification plans , and production ramp activities
  • •Develop and present manufacturing risk assessments and mitigation strategies to program leadership

Technical Leadership & Mentorship

  • •Serve as the technical SME for all PCBA process-related topics across the organization
  • •Mentor and coach junior and mid-level manufacturing engineers, technicians, and operators
  • •Lead technical reviews, design reviews, and process audits with internal and external stakeholders
  • •Develop and deliver training programs on PCBA processes, IPC standards, and quality

Quality, Compliance & Risk Management

  • •Ensure all PCBA processes comply with IPC standards (IPC-A-610, IPC-7711/7721, IPC-J-STD-001) and medical device regulatory

Supplier & Contract Manufacturer Management

  • •Lead qualification and ongoing oversight of contract manufacturers (CMs) and PCBA suppliers
  • •Conduct supplier audits and technical reviews to assess process capability and quality performance
  • •Define supplier quality

Continuous Improvement & Innovation

  • •Champion Lean Manufacturing and Six Sigma methodologies to drive waste reduction and process efficiency
  • •Lead or participate in kaizen events, value stream mapping , and other continuous improvement initiatives
  • •Identify and implement automation and digitalization opportunities in PCBA manufacturing processes
  • •Track and report on yield, defect rates, cycle time , and other key PCBA process metrics

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