QA Engineer, Product Development

QA Engineer - Product Development

Please apply in English only

*Please note: This position isn't a QA test/ Automation/ V&V engineer

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

QUALIFICATIONS/KNOWLEDGE:

Qualifications:

BS.c or MS.c degree in engineering or other discipline

Knowledge:

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

OTHER:

Ability to lift up to 20 pounds

Must have good written and oral communication skills

Highly organized and strong attention to detail

ABOUT NOVOCURE:

Our vision

Patient-forward: aspiring to make a difference in cancer.

Our patient-forward mission

Together with our patients, we strive to extend survival in some of the most aggressive forms of cancer by developing and commercializing our innovative therapy.

Our patient-forward values

– innovation

– focus

– drive

– courage

– trust

– empathy

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