Engineer

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Company: Katalyst HealthCares and Life Sciences

Location: Los Angeles, CA 90011

Description:

Roles & Responsibilities:
  • 4-6 years Minimum bachelor's or master's degree in a health-care related field
  • Strong knowledge of GMP (Good Manufacturing Practices) and ISO 13485 standards, along with regulatory affairs.
  • Strong creative, analytical, and problem-solving skills.
  • Proficient in interpreting data and compiling detailed reports.
  • Expertise in Design Quality, Good Manufacturing Practices (GMP), CAPA/NC, Statistics, DFMEA, PFMEA, CAD, Root Cause Analysis, and Manufacturing Processes.
  • Expertise in statistical analysis and root cause analysis.
  • Strong CAD skills (preferred: AutoCAD and SolidWorks).
  • Experience in fixture design, FMEA creation, and report writing.
  • Knowledge of Post Market Surveillance (PMS) and PLM tools (Windchill).
  • bility to observe, understand, and optimize manufacturing processes.
  • Excellent interpersonal, communication, organizational, and project management skills.
  • Proficiency in Windows-based software (Word, Excel, PowerPoint, email, and web browsers).
  • bility to work efficiently, meet deadlines, and communicate project status effectively.

Skills:
  • Investigate field return products and perform root cause analysis.
  • Optimize manufacturing processes and work with stakeholders to reduce scrap.
  • Identify and implement process improvement opportunities.
  • Support design enhancement initiatives.
  • Collaborate with cross-functional teams (engineering, manufacturing, marketing, and suppliers).
  • Create Engineering Change Orders (ECOs) to update documentation in the PLM system (Windchill).
  • dhere to company policies, procedures, and training requirements.

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