The role will involve management of all aspects of product registrations (Worldwide), regulatory approvals/submissions, licences and CE marking and managing relationships with the regulatory authorities. Additionally this will include maintaining processes for submissions, interim notifications and maintaining records on product registrations and regulatory requirements.
-Reporting, Financial Control and Contractual Governance -Management of Cash Flow Forecasting and the re-forecasting process -Trend analysis and the early escalation of anticipated adverse variances -Ensuring reporting is consistent with internal financial reporting and fulfils all regulatory requirements
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The role will involve management of all aspects of product registrations (Worldwide), regulatory approvals/submissions, licences and CE marking and managing relationships with the regulatory authorities. Additionally this will include maintaining processes for submissions, interim notifications and maintaining records on product registrations and regulatory requirements.
Head of Regulatory Affairs Job Summary: • Managerial leadership of the Regulatory Affairs and Pharmacovigilance departments to deliver the goals for the company projects and products; • Provide leadership on.
Regulatory Affairs Executive / Regulatory Affairs Assistant / Medical Devices Bromsgrove, Worcester £Competitive salary depending on skills and knowledge Our client, a well established UK manufacturing company supplying products and services for Cardiology, Radiology and Renal procedures in the UK and worldwide is seeking a Regulatory Affairs Executive to join their team based in Bromsgrove.
My client is dedicated to improving the health, quality of life and well-being of people through the development, manufacture and supply of the highest quality liquid medicines.
Key Requirements *Experience of regulatory submissions and licensing support. *Experience of Regulatory Affairs within a clinical trials organisation (CRO). *Regulatory submissions experience in the EU and ROW *Good experience of the preparation of marketing authorisation applications and maintenance activities.
The Regulatory Affairs Manager will ensure the business maintains its competitive lead with regard to knowledge and understanding of global legislation in the field of named patient programmes and compassionate use.
A B Resourcing has been appointed to recruit a Senior Regulatory Affairs Associate on behalf of this global organization based in the West Midlands. The main function of the role is to obtain and manage marketing approvals and product licenses throughout the business's operational areas within EMEA.
Regulatory Affairs Specialist, Medical Devices.This global market leader specialises in developing, manufacturing and supplying Orthopaedic devices for the Medical Devices sector. Due to recent expansion they now have an exciting opportunity for an International Regulatory Affairs Specialist to join their highly successful team in South Wales.
Regulatory Affairs Specialist, Medical Devices. This global market leader specialises in developing, manufacturing and supplying Orthopaedic devices for the Medical Devices sector. Due to recent expansion they now have an exciting opportunity for an International Regulatory Affairs Specialist to join their highly successful team in South Wales.
I am now recruiting for a Regulatory Specialist/Engineer to join a global leader in the orthopaedics market, on an 18month fixed term contract. My client specialises in design and manufacture of implants for replacement hips, knees, shoulders, bone cements etc and orthopaedic surgical instruments.
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