Quality Control Inspector

Vor 6 Tagen

Root, Schweiz Novocure Vollzeit

Location: Root D4, CH, 6039Novocure 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.

To support our team in Root, Switzerland are looking for a

**Quality Control Inspector**

In this position you will be responsible for supporting Novocure’s quality inspection activities of medical devices. Those activities include conducting incoming, in-process and final inspection acceptance activities through visual, mechanical and electrical testing.

**Your responsibilities**:

- Inspection of incominc, in-process and finished medical devices and components for conformance to specification.
- Initiate and participate in resolution of non-conforming materials.
- Responsible for final product release sign-off
- Trending of incominc, in-process and final inspection data.
- Assist in shipping and receiving as needed.
- Ensurance that activities comply with the applicable quality system requirements

**Your profile**:

- Quality inspection experience ideally in Medical Devices or any other regulated environment.
- Good written and spoken English communication skills.
- Ability to independent, detail oriented work according to instructions.
- Proficient in Microsoft Office.
- Ability to perform physical work that requires standing and sitting for extended periods of time.
- Knowledge of FDA and ISO standards for medical devices is a plus

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