Join to apply for the Quality Inspector role at Vision RT Ltd
Vision RT is a rapidly growing MedTech company transforming radiation therapy for cancer patients. We are the inventors of, and the market leaders in, Surface Guided Radiation Therapy (SGRT). Our SGRT solutions are used in 24 out of the 25 “Best Hospitals for Cancer,” as tracked by US News & World Report.
We’re one of Britain’s fastest-growing private tech companies, recognised by the 2025 Sunday Times 100 Tech list and winner of a 2024 King’s Award for Enterprise. Vision RT operates as part of William Demant Invest A/S, offering the security of a large global enterprise with the agility of a startup.
About the role
We are seeking a Quality Inspector for Goods Inwards and electromechanical items to join our Quality and Regulatory team. In this role, you will help ensure incoming components meet defined specifications and follow the non-conformance process to disposition when failures are identified.
Key Responsibilities
* Use risk-based sampling techniques to inspect incoming electronic components, assemblies and other goods to ensure the company’s specifications are met.
* Identify inspection criteria based on drawings and trends.
* Raise and escalate any defects or non-conformities identified during inspections of parts or records.
* Manage tools and equipment per company maintenance and calibration procedures.
* Liaise with suppliers on corrective action requests and rework.
* Maintain and update supplier and non-conforming product records.
* Work collaboratively with other teams within the Quality & Regulatory Compliance department and with Operations, Purchasing, Production and Process Engineering.
* Act as an internal and supplier auditor to ISO 9001 and ISO 13485.
* A degree in electromechanical or electronics engineering, or equivalent work experience.
* Minimum of 1 year experience of Product Quality Inspections or in a similar role.
* Practical knowledge of engineering drawings and methods.
* Knowledge of engineering measuring tools.
* Strong attention to detail, and ability to prioritise and plan tasks.
* Analytical and problem-solving skills.
* Ability to work independently and collaboratively.
* Competent in Microsoft Office products.
* Fluent in written and spoken English.
* Experience in Medical Device Quality Management Systems ISO 13485.
Seniority level
* Mid-Senior level
Employment type
* Full-time
Job function
* Quality Assurance and Engineering
Industries
* Medical Equipment Manufacturing, Appliances, Electrical, and Electronics Manufacturing, and Computers and Electronics Manufacturing
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