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Senior or Manufacturing Engineer

Job in Irvine, Orange County, California, 92713, USA
Listing for: BioTalent Ltd
Full Time position
Listed on 2026-08-25
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer, Lean Manufacturing / Six Sigma
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Lean Manufacturing / Six Sigma
Salary/Wage Range or Industry Benchmark: 120000 - 160000 USD Yearly USD 120000.00 160000.00 YEAR
Job Description & How to Apply Below
Position: Senior or Staff Manufacturing Engineer

Own the technical launch of a brand-new medical device production line, from first specs through full qualification and ramp-up. This is a hands-on, high-visibility role for someone who wants to be the go-to technical owner for a line — not just a contributor to one.

Responsibilities:
  • Line specs, layout, capacity, cycle time, and staffing to meet business needs
  • Production builds — component availability, design configurations, special builds
  • Key production metrics: yield, scrap, throughput, cycle time, OEE, uptime, process capability
  • Design transfer from R&D into operations — bridging development through qualification and launch
  • Equipment procurement, installation, commissioning, and ramp-up
  • PFMEAs, control plans, process risk assessments, and validation protocols (IQ/OQ/PQ)
  • Continuous improvement, capacity expansion, and cost-reduction initiatives
Required Experience:
  • Bachelor's in Mechanical, Manufacturing, Biomedical, Industrial, or Electrical Engineering
  • 5+ years in manufacturing or process engineering
  • Direct experience standing up and managing a new production line for a medical device — not just operating an already-mature line
  • Strong grasp of line design efficiency and line balancing (identifying bottleneck/slowest equipment, determining trade-offs on equipment speed)
  • Hands-on with equipment specification, installation, commissioning, and process validation
  • Strong grasp of DOE, SPC, process capability, and root-cause analysis
  • Comfortable owning cross-functional communication across Manufacturing, Quality, R&D, Ops, and Supply Chain
  • Medical device or other regulated manufacturing background
  • ISO 13485, process validation, and manufacturing risk management knowledge
  • Experience with automated assembly, dispensing, bonding, inspection, packaging, or test equipment
  • Lean/Six Sigma, OEE, PFMEA, and control plan experience

On-site in Irvine, CA — regular cleanroom work, with frequent commute to San Diego for business meetings

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Position Requirements
10+ Years work experience
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