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Regulatory Affairs Specialist
- London, South East England
- up to £50,000 per annum, negotiable, inc benefits
- 8 applications
- Job type: Permanent, full-time
- Date:
- Reference: 21135696
Regulatory Affairs Specialist - Oncology - Based South London
This company are leading the way pioneering significant innovations and clinical solutions for treating cancer and brain disorders. The company develops sophisticated state of the art tools and treatment planning systems for radiation therapy and radiosurgery, as well as workflow enhancing software systems across the spectrum of cancer care.
This role is to support the Quality and Regulatory Affairs Manager in achieving the company's regulatory goals and objectives, by proactively supporting the organization in achieving the necessary regulatory submissions needed for targeted market areas. You will need to develop and maintain worldwide regulatory knowledge in the preparation of regulatory submissions and registrations for existing and new products.
To be considered for this role, you will need to show an:
*Ability to interpret, adapt & provide guidance on product regulation.
*Methodical thinker able to interpret regulatory requirements into meaningful business requirements
*Preferably knowledge, experience and proven track record in Regulatory Affairs.
*Good communication skills enabling independent and interactive working across the organisation.
*Professional integrity.
*Able to work within a global multi-cultural environment.
Key words - Medical Physics, Oncology, Radiation therapy, Medical Technology, Linac Beam, linear acclerator, Radiation Therapy, regulatory affairs, regulatory submissionst
Delta Consultants - Scientific and Medical Recruitment - Applying the Art of Recruitment Science
Scientific Sales - Medical Sales - Laboratory Sales - Technical Sales - Service EngineersDelta Consultants Ltd is acting as an Employment Agency in relation to this vacancy.
This company are leading the way pioneering significant innovations and clinical solutions for treating cancer and brain disorders. The company develops sophisticated state of the art tools and treatment planning systems for radiation therapy and radiosurgery, as well as workflow enhancing software systems across the spectrum of cancer care.
This role is to support the Quality and Regulatory Affairs Manager in achieving the company's regulatory goals and objectives, by proactively supporting the organization in achieving the necessary regulatory submissions needed for targeted market areas. You will need to develop and maintain worldwide regulatory knowledge in the preparation of regulatory submissions and registrations for existing and new products.
To be considered for this role, you will need to show an:
*Ability to interpret, adapt & provide guidance on product regulation.
*Methodical thinker able to interpret regulatory requirements into meaningful business requirements
*Preferably knowledge, experience and proven track record in Regulatory Affairs.
*Good communication skills enabling independent and interactive working across the organisation.
*Professional integrity.
*Able to work within a global multi-cultural environment.
Key words - Medical Physics, Oncology, Radiation therapy, Medical Technology, Linac Beam, linear acclerator, Radiation Therapy, regulatory affairs, regulatory submissionst
Delta Consultants - Scientific and Medical Recruitment - Applying the Art of Recruitment Science
Scientific Sales - Medical Sales - Laboratory Sales - Technical Sales - Service EngineersDelta Consultants Ltd is acting as an Employment Agency in relation to this vacancy.
