QualityAssurance Specialist is required by a medical device manufacturers based at Oxford Science Park, Oxford, OX4. As QualityAssurance Specialist you will be responsible for providing qualityassurance, regulatory guidance across the business including manufacturing, supply chain and engineering. Other responsibilities as QualityAssurance Specialist include: Provide support to … new product development activities and processes Review and approve Design and Development documentation Review and approve Change Control documentation for QualityAssurance Support the maintenance of Quality System documentation Analyse and communicate proposed, new or changing requirements Review and approve CAPA documentation Provide support to routine manufacturing activities, projects, development … and training Experience required: Experience working in QualityAssurance Experience operating in ISO9001 environment Excellent working knowledge of document management systems, change control and CAPA systems Knowledge and experience of working in an ISO13485 environment is advantageous Good team player and able to work in a fast-paced environment with more »
Forums and general briefings Quality Be responsible for managing and producing ITPs and ensure they are signed off by relevant parties Ensure that the QA File is produced and maintained Close out any technical queries Ensure as-builts and O&M manuals are submitted to the client on completion Key more »
The Role: We seek a driven and experienced UX Researcher to join an expert Software Engineering team and work closely with the Product and QA Teams. As the UX Researcher, you will work on various interesting technical projects and strive to produce easy-to-use high-quality, robust applications. You more »
in the review of imaging protocols, systems of work and contribute suggestions and ideas for their improvement. To be involved in the QualityAssurance (QA) regime of Ultrasound equipment, undertaking tests and reporting faults as per the QA protocol. Support the Information Technology (IT) Department through timely reporting of IT … practices, resulting from evidence originating from both within and outside Diagnostics. Participate in all relevant Audits, modifying practice if required. Assist in implementation of QA and Clinical Governance to ensure quality standards are achieved. Ensure continuing familiarization with the current QA measures in place within the Department. To attend Clinical more »
and machine learning, the cloud, and radio-frequency identification (RFID). Product Compliance An expert knowledge of design for manufacture and product approval processes. QualityAssurance Development and implementation of qualityassurance and regulatory compliance procedures for products. Please note: Only candidates with the relevant skills and experience will be more »
Greater Oxford Area, United Kingdom Hybrid / WFH Options
Practicus
hand person to the Head of Quality, deputising for them, sharing responsibility and leading the team when required. The ideal person will have strong QA and managerial experience within pharma and GCP, someone who is willing to be hands-on and into the detail expected when operating within a startup … environment. Responsibilities: Ensuring GCP is maintained and articulated successfully across the business Taking a lead QA role in assessment and tracking of serious breaches Leading the quality team when Head of Quality is absent Report up to senior leadership and represent QA in reporting What you will bring: Roughly 7+ … years working in a leadership QA position Outstanding knowledge of GCP, TFA and FDA regulations Strong management skills A desire to be hands-on and into the thick of things Logistics: Salary of around £95,000 pa. + benefits 2-3 days a week in the office, rest from home more »