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Taylorollinson
Oxford, Oxfordshire
In Vitro Diagnostics – Regulatory Specialist Location: Oxfordshire Duration: 9 month FTC Salary: Annual salary equivalent of £40-50,000 (pro-rated for 9 months) Sector: Diagnostics Our client is a global biotechnology company specialising in the development of immunological products to diagnose and monitor patients with immunologically control
Job Source: Taylorollinsontaylorollinson Ltd
United Kingdom
In Vitro Diagnostics - Regulatory Specialist Location: Oxfordshire Duration : 9 month FTC Salary: Annual salary equivalent of £40-50,000 (pro-rated for 9 months) Sector: Diagnostics Our client is a global biotechnology company specialising in the development of immunological products to diagnose and monitor patients with immunologically controll
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Job Source: Bond WilliamsCpl Life Sciences
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Job Title: Senior Regulatory Affairs and Clinical Lead Job Type: Full-time, permanent position Location: West Oxfordshire, (On-site) Remuneration: £100,000 + This is an excellent opportunity to join a leading medical device manufacturing that is the world leader in Glucose Monitoring, their ranging product portfolio, develops and manufactures
Job Source: Cpl Life SciencesCpl Life Sciences
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Job Title: Senior Regulatory Affairs and Clinical Lead Job Type: Full time, permanent position Location: West Oxfordshire, (On-site) Remuneration: £100,000 + This is an excellent opportunity to join a leading medical device manufacturing that is the world leader in Glucose Monitoring, their ranging product portfolio, develops and manufactures g
Job Source: Cpl Life SciencesOxford
£ 40000 - 50000/annum
In Vitro Diagnostics – Regulatory Specialist
Location: Oxfordshire
Duration: 9 month FTC
Salary: Annual salary equivalent of £40-50,000 (pro-rated for 9 months)
Sector: Diagnostics
Our client is a global biotechnology company specialising in the development of immunological products to diagnose and monitor patients with immunologically controlled diseases.
The role:
An opportunity has become available for an Regulatory Specialist, experienced in Diagnostics, to join company and support the Global Regulatory activities in order to facilitate timely approval of new and existing products.
Core duties will include:
* Support with verification and validation activities to support global regulatory requirements.
* Assist the quality and regulatory team in preparation of documents for the Global IVD regulations.
* Maintenance of international quality certifications to ensure compliance (ISO13485, ISO17025, GMP)
* Assist with communication with Regulatory authorities to ensure compliance with IVD regulations
* Support with regulatory communications internally and across departments.
Experience expectations:
The successful applicant will ideally have;
* Prior experience as a Regulatory Specialist within IVD or Medical Devices
* Excellent understanding of ISO13485, ISO17025 and cGMP
* Familiarity in regulatory submission processes within Medical Devices or diagnostics.
* Familiarity with EMEA and LAT...
Email Alert for In Vitro Diagnostics - Regulatory Specialist jobs in Oxford
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