3+ YOEBA/BS and 3+ years in regulated medical device or biopharma document control or quality records role; experience with Propel/eQMS, SharePoint, and quality systems (21 CFR Part 820, ISO 13485).
NokiaNYSE: NOK: Sells telecommunications infrastructure and software for global network operators.
Develop and deliver training for photonic semiconductor manufacturing, manage document lifecycle and records, administer the LMS, conduct audits and assessments, ensure ISO and regulatory compliance, and support site ramp-up.
Quality Control Inspector (QA/QC) (Ft. Hunter Liggett, CA)
Fort Hunter Liggett, California, United States
$39/hrOnsiteFull Time
PD Systems: Provides logistics, engineering, training, and maintenance to military agencies.
High school diploma, valid CDL-A, ability to inspect heavy equipment, operate forklifts and hoists, use micrometers and gauges, document inspections, and communicate in English; able to lift 50 lbs.
Heron Power: Developing solid-state transformers and power electronics to modernize electrical grids.
Organized, methodical candidate with basic electrical/controls knowledge; ability to wire panels, document work, follow engineering conventions, and collaborate. PLC/HMI exposure and sheet-metal or schematic experience are nice-to-haves.
Claude, Microsoft PowerPoint, Microsoft Excel, HTTP/REST, PLC, HMI, AutomationDirect
Project Solutions: Provides project management and engineering services for government infrastructure.
OSHA 30-hour, construction inspection and documentation experience, quality assurance/quality control oversight, submittal/RFI review, safety monitoring, and project administration coordination.
Microsoft Word, Microsoft Excel, Microsoft Teams, Microsoft Project, Primavera
5+ YOE5+ years design quality experience in medical devices, knowledge of design controls, risk management, ISO 13485, FDA QMSR, IEC 60601-1, strong documentation and audit skills.
Imperative Care: Develops medical devices for stroke and vascular disease treatment.
8+ YOEBachelor's in engineering and 8+ years developing flexible medical device instruments or equivalent; experience with statistical analysis (Minitab), CAD (SolidWorks, ProE), PLM, documentation control, and leading cross-functional teams.