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Responsible for the provision of medical affairs support to the sales, marketing and regulatory teams in OU UK & Ireland to ensure we meet/exceed our targets and we are compliant with all relevant legislation and codes of practice.
The SAM is responsible to work closely with Clinical Affairs as well as other ADC departments and projects to ensure superior customer support. It will also require an in-depth knowledge of the difference between making recommendations in therapy based on validated standards of clinical affairs.
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Senior Manager Regulatory Affairs - South, South EastSenior Manager Regulatory Affairs c65k South East AF/016203A Senior Regulatory Affairs Manager is urgently required have primary responsibility for management of Regulatory Affairs activities and obtaining and maintaining the required regulatory approvals for products, including clinical trial approvals.
Head of Regulatory Affairs - Surrey, SurreyHead of Regulatory Affairs - Medical ConsumablesOur client is a provider of manufactured and bought in goods to a client base that is truly global.
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.
Quality Assurance Manager & Regulatory Affairs Manager Expanding Medical Devices Company based in the North East is currently seeking a Quality Assurance Manager on a 6 month contract. As the senior manager youre responsibilities will include: Maintaining and developing the Quality and Regulatory functions for the site.
Role: Regulatory Affairs Specialist / Regulatory Associate / Senior RA Specialist Salary: £33,000 - £38,000 Location: Hampshire Regulatory Affairs Specialist / Regulatory Associate / Senior RA Specialist wanted for an immediate start at a leading manufacturer of Medical Devices.
Regulatory Affairs Manager - Cambridge - PermanentMy client is a global CRO based in Cambridge urgently requiring a Regulatory Affairs Manager with extensive experience working in a CRO.
A Medical Device company based in Surrey is currently looking for an experienced Regulatory Affairs Coordinator to work on submissions and registration with new markets.You must have a Medical Device background and have in depth knowledge of dealing with regulatory submissions.
We currently require a Senior Regulatory Affairs Device manager for one of our International clients. They require a contractor to join their team for a 6 month interim period.Ideally a suitable will be able to begin asap.
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.
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