QA Engineer, Product Development

QA Engineer - Product Development

Please apply in English only

Novocure is a global medical device company with R&D based in Haifa.

The company is growing quickly as it commercializes TTFields therapy: a novel treatment for aggressive cancers using alternating electric fields.

We are looking for a Quality Assurance Engineer who will join our R&D center and support Novocure’s medical device product development activities by providing a technical review of design input requirements, design descriptions, and other product design and test documentation.

This position involves frequent communication and coordination with Project Management, engineering and quality team members in Portsmouth NH, Switzerland, and Israel.

This is a full-time, exempt position which reports to a Senior Quality Engineer- Product Development (or higher) and will located in our Haifa, Israel office.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Provide advice, guidance, and training as needed to ensure product realization activities and documentation meet quality system requirements
• Review engineering and test documents to ensure they meet Novocure quality system requirements consistent with applicable regulations, standards, and guidance
• Provide constructive feedback to improve design and test documentation
• Participate in product and process risk analysis activities
• Collaborate in requirements development and derivation
• Participate in corrective and preventative action activities
• Participate in design reviews
  
  

• 2-7 years of related experience
• At least 1 year of experience in medical device product development- preferably
• Demonstrated technical writing skills
• English language mastery and fluency
• Experience with risk analysis and risk management
• Experience writing and reviewing design input requirements
• Experience writing and reviewing design verification and validation protocols
• Critical thinking and decision-making, including the ability to recognize when to ask questions
• Familiarity with Quality System Regulation, Medical Device Regulation, ISO 13485, and ISO 14971
• Able to work in a team environment and execute responsibilities with some direct supervision
  
  

• Ability to lift up to 20 pounds
• Must have good written and oral communication skills
• Highly organized and strong attention to detail