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Staff Engineer, Instrument Manufacturing

Job in San Diego, San Diego County, California, 92189, USA
Listing for: UNAVAILABLE
Full Time position
Listed on 2026-05-23
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer, Electronics Engineer, Process Engineer
Salary/Wage Range or Industry Benchmark: 145000 - 175000 USD Yearly USD 145000.00 175000.00 YEAR
Job Description & How to Apply Below

Overview

Job Summary

The Staff Manufacturing Engineer applies advanced technical insight, hands‑on experience, and deep knowledge of electrical systems to support complex Manufacturing Engineering activities focused on instrument electronics and printed circuit board assemblies (PCBAs) in the instrument area. This role is responsible for solving multifaceted issues in new product design transfer, manufacturing process development and optimization for medical diagnostic instruments, electrical integration, sustaining engineering, and daily production operations.

The Staff Manufacturing Engineer will lead cross‑functional teams on continuous improvement projects, develop and execute validation protocols and final reports, and drive manufacturing activities to ensure high‑yield, reliable production of complex electromechanical instruments.

The annual base salary range for this role is currently $145,000 to $175,000. This is a bonus‑eligible position. Individual employee compensation will ultimately depend on factors including education, relevant experience, skillset, knowledge, and particular business needs.

Responsibilities

Key Accountabilities

  • Function as a lead team member for design control project teams; ensure design requirements are met and comply with applicable standards.
  • Work as a lead project team member to complete all activities needed to conclude projects per plans.
  • Develop and implement process controls for new products and for transfer to manufacturing.
  • Develop statistically based sampling plans for design verification, design and process validation activities, new/existing product test methods, and incoming inspection to ensure they meet their predetermined requirements.
  • Oversee validation project teams; prepare agendas, issue meeting minutes, and participate in development of quality plans.
  • Write, review, and approve validations (installation qualification IQ/operational qualification OQ/performance qualification PQ protocols, SOPs, technical reports and final reports) for new products, processes, and equipment; ensure systems, utilities, and processes comply with the FDA and industry standards.
  • Function as an advanced support resource; lead training initiatives of department staff as directed.
  • Provide statistical analysis of process and test data to support validation reports and continuous improvement.
  • Ensure all projects/processes are following FDA, Good Manufacturing Practices (GMP), Quality System Requirement (QSR), ISO‑13485:2003 and other applicable requirements.
  • Actively participate in FDA inspections, ISO audits, and internal/customer audits as a subject‑matter expert on instrument electronics.
  • Provide cross‑functional support by delivering required technical documentation and data to meet compliance needs.
  • Identify and implement opportunities for continuous improvement in instrument yield, cycle time, and first‑pass quality.
  • Coordinate activities with cross‑functional departments, external CMs/vendors, and customers.
  • Maintain fiscal responsibility and budget compliance.
  • Ensure and maintain compliance with the company’s quality system requirements through training and adherence to policies, procedures, and processes.
  • Other duties as assigned.

Networking/Key relationships

  • To be determined based on business needs.
Qualifications

Minimum Knowledge & Experience for the position:

  • Bachelor’s degree in Electrical Engineering (strongly preferred) or equivalent; advanced degree a plus.
  • A minimum of Ten (10) years of progressive manufacturing engineering experience in a regulated medical device environment, with significant hands‑on focus on printed circuit board assemblies (PCBAs), electronics manufacturing, and instrument production.

Skills & Capabilities:

  • Six Sigma Green Belt or Black Belt methodology a plus.
  • Strong Electrical Engineering background with deep proficiency in electrical schematics, BOM management, and electromechanical instrument integration.
  • In-depth knowledge of instrument electronics and PCBA technologies, including sustaining support, integration, and technical oversight of contract manufacturers.
  • Excellent troubleshooting and root‑cause analysis skills for electrical and…
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