Medical devices regulatory affairs jobs in Croydon

Well known and respected Wellness brand are looking for a Senior Regulatory Affairs Manager who has experience in Herbal Medicines (ideally) Medical Devices and CosmeticsAs a Senior Regulatory ...

Up to £50,000 Senior Regulatory Affairs Officer opportunity working for a growing pharmaceutical company that specialising in medicinal, non-medicinal, medical devices, and OTC products. The ...

You will be responsible for becoming the subject matter expert on medical devices within the ... You will support the European Head of Regulatory Affairs and Pharmacovigilance in specific projects ...

... medical products. * Contributing regulatory guidance in order to enhance product development ... Previous experience in Regulatory Affairs and Compliance particularly within pharmaceutical ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

... Medical Device Regulations, International Standards, and Customer Requirements and that this is ... Responsibilities · Responsible for maintaining and supporting the promotion of regulatory affairs ...

Medical Diagnostics Design Engineer - Electromechanical Design - London A new Medical Devices start ... Regulatory Affairs, Quality Assurance, and Field Service Engineering sectors.

... devices. * Tech - working across some of the most exciting tech policy areas, including ... At least 3 years' experience gained from working in consultancy, in-house, thinktank, regulator or ...

Technical background within software medical devices with a strong understanding of the regulatory function, and a good knowledge of related quality, engineering, clinical, safety, and post-market ...

Bachelor's degree in a relevant field (e.g., Engineering, Life Sciences, Regulatory Affairs) * 2 years' experience in quality and regulatory affairs within the medical device industry, preferably ...

From research and development to regulatory affairs and sales, you will work closely with clients ... medical devices, and healthcare. * Build and maintain strong relationships with clients ...

... affairs, meetings, and HCP and patient education. They cover a variety of therapy areas including ... In depth knowledge of the pharmaceutical industry and associated regulations. * Superb relationship ...

... and Regulatory Affairs to join one of their clinical diagnostic sites in a permanent, full-time ... medical microbiology, medical laboratory sciences or biomedical science. You will need strong ...

Health-care regulatory body Do you have an interest in politics and current affairs is so this ... high standards in medical education and practise. Apply now to be part of a dynamic and ...

... medical devices as well as an understanding of how and why the devices can support healthcare delivery. * Extensive knowledge of medical device standards safety regulations pertaining to their ...

... Medical Device, IMP management, Regulatory Affairs and Pharmacovigilance · Experience in Monitoring, Quality Assurance and/or Good Clinical Practices · Exposure to inspections COMPETENCIES · ...

Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners ...

... chemicals, medical devices and equipment, automotive, telecoms, electronics and software. Our ... and regulatory environments, as well as for resolving contractual disputes involving such ...

... regulatory affairs, to align financial goals with operational objectives in the life sciences ... medical device companies. Proclinical Staffing is an equal opportunity employer.

... Regulatory Affairs, Clinical Development, Medical Affairs and Quality Assurance - all functions are booming and there is a real demand in the US for international talent to support the market. The ...

Prior experience working in Medical Devices or Pharmaceuticals is essential. Role Overview ... Knowledge of relevant regulations and standards - MDD/MDR, ISO13485 , cGMP. * Access to own ...

Collaborates with local medical affairs colleagues on country specific studies and initiatives * Provides knowledge and expertise on country specific regulations and site experience and suitability ...

Responsibilities: • Conduct Human Factors studies to assess the usability of medical devices ... Create regulatory paperwork such as human factors summary reports, threshold analyses, and ...

From orchestrating on-site meetings, congresses, and symposia to developing medical affairs content ... Familiarity with ABPI regulations. * Experience with Veeva, Promomats and CRM platforms. 🎁 ...