Novocure is a global publicly-traded commercial-stage oncology company developing a profoundly different cancer treatment therapy called tumor treating fields (TTFields) for patients with solid tumors. TTFields therapy is a non-invasive, novel, antimitotic treatment modality which utilizes proprietary technology attempting to slow or reverse tumor progression by inducing tumor cell death. Novocure's commercialized product, Optune, is approved for the treatment of adult patients with glioblastoma (GBM) in the USA, Europe and Israel. Novocure has ongoing or completed clinical trials and is further expanding its efforts into several other solid tumor indications - non-small cell lung cancer, pancreatic cancer and other types of solid cancers.
We are currently looking for a Software Design Quality Assurance Engineer to join our Kraków office.
As a Software Design QA Engineer, you will work with software development and quality assurance teams to implement best practices.
This is a full-time, exempt position located in our Krakow Poland office and reports to the Software Quality Assurance Manager.
RESPONSIBILITIES :
- Review requirements, specifications, design documents, validation plans and report, user acceptance protocols, test protocols and reports, traceability matrices and other documentation as required and provide feedback.
- Provide expertise in establishing good software requirements, specifications, detailed design, verification and validation protocols and planning documentation.
- Support development teams on the validation of software tools.
- Ensure the delivery of high-quality products (including requirements, design documentation, testing, and deployment procedures) while adhering to medical device industry standards and regulations
- Work with cross-functional teams to drive projects to completion
YOUR PROFILE : Qualifications :
Bachelor’s degree required, preferably in computer scienceA hands-on background in software development - advantageBackground in radiation oncology or medical industry – advantageKnowledge :
4+ years of experience developing software in highly regulated environments, including the medical and safety-critical industriesStrong knowledge of software QA methodologies, tools, and processesKnowledge of up to date related standards and regulationsSkilled in managing traceability matrixes between all SDLC documentsTop level knowledge of test types and strategies : unit, integration, system, performance, stress etc.Experience with IEC 62304 – big advantageKnowledge of Software Configuration Management, CI and CD technologiesExperience working in an Agile / Scrum as well as waterfall development process and the implications coming from the regulatory standardsExcellent Documentation Skills and experience operating under Document ControlProficient communication skills in English (verbal and written)Benefits :
Performance related bonusLife InsuranceFree fruit & cookies delivered for office staffMultisport cardPrivate Medical careand more