Trabajos medical devices regulatory affairs en Beckenham

Work closely with cross-functional teams, including marketing, medical affairs, and market access ... Ensure all activities comply with company policies and regulatory requirements Benefits: · Career ...

UK CW Regulatory Affairs Manager (Inside IR35) This role will support one or more products from a ... medical device companies. Proclinical Staffing is an equal opportunity employer.

We are seeking a motivated Junior Consultant with 2-5 years of experience in Regulatory Affairs ... Create, review, and manage technical files and documentation for medical devices. * Compliance ...

Provide medical leadership and guidance to cross-functional teams, including Clinical Development, Regulatory Affairs, Marketing, and Market Access, to ensure successful product development and ...

Benefits on Offer: * Private medical insurance (for you, your partner and children) * Life ... Previous experience in the financial services industry/financial policy and regulation. * Excellent ...

... Regulatory Affairs or Companion Diagnostics. * Strong and proven team leadership skills * Deep knowledge in drug development and development of medical devices is a plus. * Strong knowledge of ...

... Affairs - to provide the essential support services that all areas of the business need, here in ... Private medical insurance (permanent employees only) * At least 25 days holiday, plus public ...

Director, Scientific Affairs Department: Scientific Affairs CNX Therapeutics is a European ... Ensure compliance with the General Data Protection regulation (GDPR) in relation to PV data ...

Customer Service Centre * Quality & Regulatory Affairs (QRA) function * Customer Engineering ... Medical equipment suppliers/manufacturers/distributors Person Specification: * Sales experience

Continues to strengthen collaboration with other departments such as PV, TMO, Regulatory, Quality ... Proven experience in Medical Information / Medical Affairs Function. Skills & Knowledge

As a Product Safety Specialist, you will be a vital member of our regulatory affairs team ... Private Medical Care * Exclusive benefits, free advice and savings from a range of retailers and ...

Collaborate with cross-functional teams, including clinical operations, regulatory affairs, medical affairs, and data management, to ensure alignment and effective communication throughout the ...

... 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 ...

Proven experience in designing and developing medical devices. * Familiarity with regulatory standards (e.g., FDA, ISO) and quality management systems. * Proficiency in CAD software, preferably ...

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

Facilitate effective collaboration and coordination among various functions involved in the launch, such as marketing, medical affairs, regulatory, market access, operations, and homecare. Ensure ...

... 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 ...

Design and conduct experiments and validation protocols to ensure the accuracy and reliability of machine learning models for medical devices. * Ensure compliance with relevant regulatory guidelines ...

Proven experience in designing and developing medical devices. Familiarity with regulatory standards (e.g., FDA, ISO) and quality management systems. Proficiency in CAD software, preferably Autodesk ...

Experience and understanding of Press & Regulatory affairs including regulations and compliance ... Private Medical and 4 x life Insurance scheme * Long service holiday scheme * Holiday purchase ...

... medical devices. * Familiarity with FDA/MDR/UK MDR medical device software regulation is essential including applicable standards such as ISO 13485, ISO 14971, IEC 62304, IEC 82304, and IEC 62366

... medical equipment and devices · Experience of Renal/Dialysis equipment is a huge advantage · Knowledge of regulations in Health & Safety and Medical Devices · A methodical approach to ...

... regulations/ standards/ guidelines for vigilance of both marketed and investigational products (incl. drugs, food supplements and medical devices). Major Accountabilities: * Manage the collection ...

... devices, and software to meet project specifications and regulatory standards. * Perform system ... Discounted private medical * Health and Well-being package * Dynamic and collaborative work ...