Regulatory Specialist - Medical Devices Jobs in London, England | Glassdoor.ca

Regulatory Specialist - Medical Devices Jobs in London, England

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  • 2.6
    Elekta – Crawley, West Sussex, South East England, England
    18 days ago 18d
    state-of-the art medical tools and treatment planning systems, is looking for a Clinical Training Specialist- Physics to join… (i.e, Linac QA, data collection and associated measurement devices, beam modeling process, treatment planning) Strong leadership…
  • i-Pharm Consulting Ltd – London, England
    4 days ago 4d
    Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). I-Pharm Regulatory is a team within… ABOUT i-PHARM REGULATORY i-Pharm Regulatory is a specialist Recruitment team working wholly within the Regulatory Affairs market…
  • 3.9
    Adzuna – London, England
    7 days ago 7d
    Our client is a high technology Medical Device company operating within the Oncology sector. They are a well recognised provider… footprint. They are looking to bring in a Quality and Regulatory Affairs Specialist who will share their passion, dedicate themselves…
  • ProClinical Ltd – Uxbridge, England
    4 days ago 4d
    major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.… Principal Regulatory Affairs Executive job will be responsible for preparing high quality documentation for all regulatory submissions…
  • 4.3
    Support Services Group – London, England
    23 days ago 23d
    call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore Consulting, on… you. Newton Colmore Consulting is a specialist recruitment company within the Medical Devices, Scientific Engineering, Scientific…
  • i-Pharm Consulting Ltd – London, England
    4 days ago 4d
    Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). I-Pharm Regulatory is a team within… ABOUT i-PHARM REGULATORY i-Pharm Regulatory is a specialist Recruitment team working wholly within the Regulatory Affairs market…
  • 3.9
    Adzuna – London, England
    13 days ago 13d
    Close Out Visits / CRO / Global CRO / Midsized CRO / Medical Devices / Devices / Pharma / Global Pharma Companies / Home-based /… CRA - Clinical Research Associate - Medical Devices - Home-based - UK i-Pharm Consulting is seeking a driven CRA with at least…
  • 4.3
    Support Services Group – London, England
    23 days ago 23d
    mechanical engineers, quality assurance and regulatory experts. The type of medical devices, you will be helping to create, will need… call Andrew Welsh, Director of Medical Devices recruitment and Scientific recruitment specialists Newton Colmore Consulting, on…
  • Professional Information – Richmond, London, England
    8 days ago 8d
    development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the… leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full…
  • 3.7
    Medtronic – Watford, East of England, England
    16 days ago 16d
    assist and support the Regulatory Affairs and Quality Manager in all aspects of medical device Regulatory Affairs relevant to the… profile 3 or more years Regulatory Affairs experience in the EMEA medical device industry (high risk classes) Post-market…
  • 3.9
    Adzuna – London, England
    2 days ago 2d
    major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Apply… Principal Regulatory Affairs Executive job will be responsible for preparing high quality documentation for all regulatory submissions…
  • i-Pharm Consulting Ltd – London, England
    9 days ago 9d
    Operations, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Biometrics. [URL removed] | Medical Affairs… permanent and contract staff to a range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs…
  • 3.7
    Barrington James Limited – London, England
    16 days ago 16d
    standards Quality background for the Pharmaceutical or medical device industry Knowledge of CSV including 21CFR Ideally, experience… management to comply with regulatory requirement and global business standards CAPA and deviation process management and review…
  • On Target Recruitment Limited – Bromley, England
    9 days ago 9d
    experience working in the pharmaceutical or in-vitro diagnostic medical devices industries - Experience in automated or part-automated… refurbishment project - Knowledge of working under other regulatory regimes (MHRA, ISO13485, or CE mark) is beneficial - Knowledge…
  • 3.2
    Adecco – Dartford, England
    7 days ago 7d
    experience working in the pharmaceutical or in-vitro diagnostic medical devices industries. *Experience in automated or part-automated… or refurbishment project *Knowledge of working under other regulatory regimes (MHRA, ISO13485, or CE mark) is beneficial. *Knowledge…
  • i-Pharm Consulting Ltd – London, England
    25 days ago 25d
    Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). I-Pharm Regulatory is a team within… ABOUT i-PHARM REGULATORY i-Pharm Regulatory is a specialist Recruitment team working wholly within the Regulatory Affairs market…
  • Professional Information – Richmond, London, England
    23 days ago 23d
    development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in the… leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full…
  • 3.7
    Amgen – Uxbridge, England
    2 days ago 2d
    of pharmaceutical/biotechnology or medical device industry Specialist knowledge of Regulatory Affairs. Strong communication skills… QC of regulatory documentation (e.g. redaction) Skills / Competencies: Bachelor’s degree and significant Regulatory CMC…
  • 3.2
    Adecco – Dartford, England
    7 days ago 7d
    experience working in the pharmaceutical or in-vitro diagnostic medical devices industries. * Experience in automated or part-automated… refurbishment project * Knowledge of working under other regulatory regimes (MHRA, ISO13485, or CE mark) is beneficial. * Knowledge…
  • 3.9
    Adzuna – United Kingdom
    8 days ago 8d
    major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Apply… Leaflet to support submissions to the Regulatory Authorities across regions, requesting medical advice from others when appropriate…
  • i-Pharm Consulting Ltd – Maidenhead, England
    8 days ago 8d
    experience in Medical Information within the pharmaceutical industry and will be an integral part of the UK Regulatory and Medical Team.… Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics. Key Words: Medical Information…
  • 3.9
    Medicines and Healthcare products Regulatory Agency – Potters Bar, England
    3 days ago 3d
    regulation of medicines and medical devices. A centre of the Medicines and Healthcare products Regulatory Agency, The National Institute… emergencies. Purpose of the role: The Specialist Service Contract Manager will manage all specialist service contracts to ensure that…
  • 3.4
    Novella Clinical – Stevenage, England
    7 days ago 7d
    successful and growing medical device regulatory team where you can demonstrate your prowess in Medical Device Regulatory Affairs. Then… experience in medical devices regulatory affairs, within industry or a CRO environment. · Extensive knowledge of medical device…
  • 5.0
    Key People Limited – London, England
    30+ days ago 30d+
    pharmaceutical/biotechnology or medical device industry -Specialist knowledge of Regulatory Affairs for a minimum of 1-2 years… years of CMC Regulatory experience and a strong knowledge of Regulatory Affairs.Responsibilities: -The Regulatory Professional…
  • PE Global – Uxbridge, England
    30+ days ago 30d+
    pharmaceutical/biotechnology or medical device industry Specialist knowledge of Regulatory Affairs for a minimum of 1-2 years… Senior Regulatory Affairs Associate for our multinational pharmaceutical client based in the Middlesex area. The Regulatory Professional…
  • i-Pharm Consulting Ltd – London, England
    4 days ago 4d
    permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs… i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and…
  • 4.4
    Swanstaff Recruitment Ltd – London, England
    30 days ago 30d+
    experience working in the pharmaceutical or in-vitro diagnostic medical devices industries. Experience in automated or part-automated… or refurbishment project Knowledge of working under other regulatory regimes (MHRA, ISO13485, or CE mark) is beneficial. Knowledge…
  • Professional Information – Richmond, London, England
    7 days ago 7d
    Follow up call intake for pharmaceutical, DS/OTC, medical food and medical device products Assist call intake staff with call management… the pharmaceutical, biotechnology, and medical device fields. We service clients globally with offices in the United States, United…
  • 3.7
    Amgen – Uxbridge, England
    3 days ago 3d
    of pharmaceutical/biotechnology or medical device industry Specialist knowledge of Regulatory Affairs. Strong communication skills… QC of regulatory documentation (e.g. redaction) Skills / Competencies: Bachelor’s degree and significant Regulatory CMC…
  • 3.2
    Thermo Fisher Scientific – Dartford, England
    8 days ago 8d
    GMP environment Demonstrable validation experience in a medical device ISO13485, biopharmaceutical (chromatography, ELISA), consumer… You will also represent the business in customer audits and regulatory inspections to demonstrate that we have compliant systems.…
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