More jobs:
Senior or Manufacturing Engineer
Job in
Irvine, Orange County, California, 92713, USA
Listed on 2026-08-25
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
Job Description & How to Apply Below
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
- 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
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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