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Senior Quality Engineer

Karwell Technologies

San Diego, CA

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JOB DETAILS
SKILLS
Analysis Skills, Cleanroom, Communication Skills, Cross-Functional, Design Verification, Detail Oriented, Documentation, File Maintenance, ISO (International Organization for Standardization), Leadership, Manufacturing Requirements, Manufacturing/Industrial Processes, Marketing, Medical Equipment, Minitab, Operations Processes, Problem Solving Skills, Process Validation, Product Development, Product Support, Quality Assurance, Quality Assurance Methodology, Quality Engineering, Quality Management, Regulations, Research & Development (R&D), Risk Management, Statistics Software, Technical Writing, Test Plan/Schedule
LOCATION
San Diego, CA
POSTED
3 days ago
Job Description:
  • The Senior Quality Engineer will perform Quality Engineering activities supporting product development and ongoing cleanroom build efforts, ensuring New Product Development (NPD) processes comply with quality systems and applicable regulatory standards.
  • The role works cross-functionally to support design verification, process validation, and commercialization activities.
Roles & Responsibilities:
  • Perform Quality Engineering activities related to product development and ongoing cleanroom build support.
  • Ensure NPD processes comply with quality system and applicable regulatory standards.
  • Update risk management and design control files and maintain relevant quality documentation.
  • Develop and execute test method validations and qualification plans.
  • Support design verification and facilitate process validation and commercialization activities related to multi-site transfer.
  • Work collaboratively with cross-functional teams including R&D, manufacturing, regulatory, clinical, and marketing.
  • Perform other duties as assigned by Leadership.
Requirements:
  • Bachelor's degree in Engineering or Scientific field with 4+ years of experience OR Master's degree or equivalent in Engineering or Scientific field with 3+ years of experience.
  • Proficient understanding of medical device operations and/or manufacturing processes (medical device experience strongly preferred).
  • Relevant experience in product development, quality assurance, and/or related fields.
  • Knowledge and understanding of Engineering and Quality principles, theories, and concepts.
  • Understanding of ISO 13485Experience developing, updating, and maintaining technical content of risk management files.
  • Basic understanding of statistical techniques; experience using statistical software (e.g., Minitab) is a plus.
  • Experience in test method development including validation and/or fixture development.
  • Solid problem-solving, organizational, analytical, and critical thinking skills.
  • Strong documentation and communication skills with attention to detail.
  • Ability to build productive working relationships across all organizational levels.
  • Ability to manage competing priorities in a fast-paced environment.

About the Company

K

Karwell Technologies

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