Medical devices regulatory affairs jobs in Watford

Front Office Team at Citadines Trafalgar Square London.Our properties operate 24/7; therefore, the department works on an early (7am-3.Night shifts are also available and required on occasion.Offer a warm welcome and departure experience to our guests, managing expectations by constantly seeking ...

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.

Partners with pharmacovigilance, regulatory affairs, in-country teams, and device QA for ... Knowledge of global regulatory requirements for pharmaceutical, medical devices and combination ...

... 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 ...

... 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 ...

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

... 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 ...

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 ...

... 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 ...

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 ...

The Senior Global Market Access Manager will report to the VP, Commercial Affairs and will be ... Supply safety data to the regulatory department for regulatory submissions. * Contribute to the ...

... medical devices, IVD and digital technology), charity and public research funders, to work in ... regulatory approval, market entry and adoption into the NHS, the UK and other global healthcare ...

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

... Affairs - to provide the essential support services that all areas of the business need, here in ... Ensuring that these new policies meet legislative and regulatory requirements * Providing subject ...

Focusing predominantly on clients within the Healthcare / Medical Devices / Pharma sector ... regulations, networking groups) Extensive experience in generating customers trading with the USA ...