Senior Design Quality Engineer

Johnson & Johnson Johnson & Johnson · Pharma · Galway, Ireland

Senior Design Quality Engineer at Johnson & Johnson in Galway, Ireland, focusing on design control, risk management, and quality system compliance for new and existing medical products. Requires a degree in engineering, 5+ years of industry experience, and knowledge of medical device regulations (21 CFR 820, ISO 13485).

What you'd actually do

  1. Ensuring Design Control and Risk Management activities comply with applicable processes and regulatory requirements
  2. Acting as a Design Quality team member supporting new product development and lifecycle management activities
  3. Providing guidance on medical device regulations and design control requirements across global markets
  4. Supporting product development teams in the effective application of design controls and risk management principles
  5. Partnering with design teams to define design inputs and outputs, support verification and validation activities, and contribute to process validation, design transfer, and launch planning

Skills

Required

  • Degree in an engineering or technical discipline
  • Minimum 5 years of experience in the medical device, IVD, or pharmaceutical industry
  • Experience working with Quality Management Systems and design control processes
  • Strong knowledge of design control, risk management, sterilization, and quality assurance processes
  • Working knowledge of 21 CFR 820 and ISO 13485, with familiarity of global regulatory requirements
  • Experience preparing for and participating in regulatory inspections (e.g., FDA, Notified Body)
  • Ability to manage multiple projects and prioritize effectively in a dynamic environment
  • Strong problem-solving skills and ability to identify and address key quality risks
  • Ability to work independently and collaboratively within cross-functional and global teams
  • Clear communication skills, with the ability to present complex information in a structured way
  • Ability to build strong working relationships across functions such as Product Development, Regulatory Affairs, Manufacturing, and Marketing

Nice to have

  • Agility Jumps
  • Business Behavior
  • Coaching
  • Compliance Management
  • Continuous Impro

What the JD emphasized

  • Minimum 5 years of experience in the medical device, IVD, or pharmaceutical industry
  • Experience working with Quality Management Systems and design control processes
  • Strong knowledge of design control, risk management, sterilization, and quality assurance processes
  • Working knowledge of 21 CFR 820 and ISO 13485, with familiarity of global regulatory requirements
  • Experience preparing for and participating in regulatory inspections (e.g., FDA, Notified Body)