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, ovarian cancer and other types of solid cancers. Eindhoven, Netherlands we are looking for a:  

Quality Control Inspector

  In this role as QC Inspector you are responsible for supporting Novocure`s quality inspection activities in the warehouse of Novocure in Einhoven and reporting to Quality Control Supervisor. This includes conducting incoming, in-process and final inspection acceptance activities as needed. Acceptance activities include visual, mechanical and electrical testing as required. Your responsibilities: •    Inspect incoming, in-process, finished products for conformance to specification. •    Initiate and participate in resolution of non-conforming materials. •    Responsible for final product release sign-off. •    Trend incoming, in-process, and final inspection data. •    Assist in shipping and receiving as needed. •    Ensure activities comply with the applicable Novocure Quality System requirements.   Your profile: •    Quality Control Inspection experience in a Medical Device regulated environment •    Knowledge of active medical equipment desirable •    Proficient in Microsoft Office •    Must have good written and oral communication skills •    Must be able to read, speak and write English •    Must be able to work in a team environment, execute responsibilities with minimal direct supervision, and have a high attention to detail •    Knowledge of FDA and ISO standards for Medical Devices is a plus •    Ability to multi-task, perform efficiently, and independently •    Standing and sitting for extended periods