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Chief Scientist

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Confidential 80000.00 British Pound . GBP Per annum

2021-12-03 08:51:20

Job location Thame, Oxfordshire, United Kingdom

Job type: fulltime

Job industry: Engineering

Job description

Our client is part of a group of market leading global medical device companies. They are experiencing rapid growth and are looking for a senior candidate to join the ranks. The Chief Scientist will lead all aspects relating to Assay, Reagent and Product Development for PT/INR testing and other projects and products of the Company.

The Chief Scientist will manage all aspects of Assay and Reagent development on all the Company's multiple projects from concept to commercialisation. This includes development and implementation of specifications, procedures and methods, verification and validation activities, clinical studies and assisting in transfer to manufacturing.

The Chief Scientist will be member of the senior management team involved in future direction of the Company and will help define new product areas applying the Companies intellectual property, as well as actively looking to enhance the Companies portfolio and helping the R&D effort.

Responsibilities:

Act as clinical and biological lead for the company
Identify, understand and communicate opportunities for applications of the company's existing and new technologies and develop product roadmaps for the company.
Assist in ensuring projects are delivered efficiently to meet the relevant standards with appropriate risk management and Quality Planning throughout
Write, review and maintain documentation relating to projects
Identify, plan and execute the required clinical studies for the company's projects
Manage and build relationships with external partners to ensure projects are delivered where external expertise is required.
Keep current in new and emerging technologies relating to diagnostic monitoringQualifications/Skills:

Either a degree in a scientific or engineering discipline or equivalent practical experience
Ideally Medical Device industry knowledge to ISO 13485, IVD Directive 98/79/EC and FDA 21 CFR part 820.
Product development of medical device and medical IVD products
Ideally leading projects under ISO 13485 from concept to manufacture
Quality and Regulatory aspects of medical devices.
Ideally Management level experience
Able to travel

To find out more about Real please visit

Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC(phone number removed) England and Wales

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