Junior Quality Engineer - Failure Investigations

DEKA Research & DevelopmentManchester, NH

About The Position

Join our dynamic team at DEKA and help solve complex technical challenges in subcutaneous drug delivery systems. As a Junior Quality Engineer focused on Failure Investigations, you will play a key role in a collaborative environment, supporting root cause investigations and driving product improvements through systematic analysis. This is a high-visibility role with direct impact on product quality, safety, and overall program success. As a key contributor to our team, the following skills are required: Technical Expertise: Ability to understand complex electromechanical systems and apply engineering principles to failure analysis Root Cause Analysis: Structured, data-driven problem solving using inductive/deductive reasoning Risk Awareness: Understanding of failure modes and their impact on product risk (e.g., risk file integration) Collaboration: Effective cross-functional communication and ability to drive alignment on root cause and corrective actions Analytical Skills: Ability to interpret complex or ambiguous data and identify meaningful patterns Self-Management: Ability to manage multiple investigations and prioritize effectively Technical Communication: Clear, concise documentation of investigations and findings

Requirements

  • BS/MS in Science or Engineering
  • Hands-on experience troubleshooting electromechanical products and systems
  • Experience with electronics test equipment (multi-meters, oscilloscopes, power supplies, microscopes)
  • Strong data analysis and problem-solving skills
  • Excellent written and verbal communication skills
  • Must have strong attention to detail

Nice To Haves

  • Experience with medical device field returns and complaint handling
  • Ability to read and interpret electrical schematics and mechanical drawings
  • Familiarity with statistical analysis tools (Minitab, JMP, etc.)
  • Experience with electromechanical device development
  • Knowledge of FDA's Quality System Regulation (21 CFR Part 820), ISO 13485 or (ISO 14971)

Responsibilities

  • Conduct multiple simultaneous field return investigations from initiation through closure, ensuring thorough root cause analysis and appropriate corrective actions
  • Participate actively in multidisciplinary investigation teams, bringing quality and accuracy to technical discussions
  • Analyze field return data, failure modes, and trends to identify systemic issues and improvement opportunities
  • Interpret investigation results and translate findings into actionable recommendations for design, manufacturing, or process improvements
  • Ensure investigation findings are properly documented and integrated into the risk management file
  • Attain and maintain comprehensive understanding of device design, manufacturing processes, and core technologies to support effective investigation
  • Peer review investigation reports to ensure accuracy and completeness
  • Contribute to continuous improvement initiatives based on investigation insights
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