Medical devices regulatory affairs jobs in GreenfordCreate job alerts

Solid experience within medical device regulatory affairs. Regulatory Director - Complex Software/Electronic Medical Devices. This Regulatory Affairs Director role reports to the VP of RA/QA with the primary goal of supporting the international registration program with the new products they have...

... Affairs Manager to join their team. You will be a confident Regulatory Lead looking to work in an ... trials and medical products. * Contributing regulatory guidance in order to enhance product ...

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

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

... Medical Devices sector. Our goal is to deliver outstanding recruitment solutions, ensuring top ... You will collaborate with cross-functional teams, including R&D, Quality, and Regulatory Affairs ...

Experience within the Pharmaceutical industry needed, preferably in Medical Affairs or a Quality, Pharmacovigilance or Regulatory department would be very beneficial Role and Responsibilities: * To ...

... Medical Devices industry. Collaborate with cross-functional teams, including R&D, Quality, Regulatory Affairs, and IT, to ensure end-to-end traceability, from requirements through to testing and ...

You will serve as the primary point of contact for internal teams and external sponsors, providing strategic advice on regulatory affairs and medical writing. As Head of Medical Writing and ...

You will serve as the primary point of contact for internal teams and external sponsors, providing strategic advice on regulatory affairs and medical writing. As Head of Medical Writing and ...

As a strategic advisor, you'll provide key insights into regulatory affairs and medical writing for internal teams and external sponsors alike. The role includes managing the medical writing and ...

Support the growth of the Medical Writing and Regulatory Affairs department, contributing to the commercial success of the organisation. * Regularly update process maps for medical writing and ...

... regulatory challenges. Will manage the most complex assets and those that potentially will require ... Lead development and execution of medical affairs strategy for Renal priority programs including ...

Senior Manager, Medical Writing - Regulatory Affairs Job Type: Permanent, full-time Location: Central London, UK - 4x a week in London Remuneration: Up to £80,000 + Benefits An exciting and rare ...

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

You will act as a point of contact for Local Medical Affairs, facilitating collaboration between ... Provide expertise in GCP or RWE data generation regulations to assess clinical study design

The role involves leadership in process development, team management, budget oversight, and collaboration with cross-functional teams including regulatory, medical affairs, and commercial departments

... medical devices, supplements, children's toys, and more-meets global regulatory requirements across the US, Canada, the UK, Europe, Japan, and Australia We seek a self-starter who excels ...

... regulations/ standards/ guidelines for vigilance of both marketed and investigational products (incl. drugs, food supplements and medical devices) from Novartis Group. * To mentor less experienced ...

Stay informed about industry developments, regulatory changes, and emerging trends affecting the ... medical devices, and related sectors. * Strong work ethic, attention to detail, and a proactive ...

... vascular devices. * Collaborate with sales and account teams to achieve targets, track product ... Ensure compliance with all quality and regulatory standards, maintaining a commitment to the ...

Our client, a leading distributor of highly regarded medical aesthetic skincare and devices, is ... You will be focused on the detail and ensure that you are compliant with regulatory requirements

Support the management team maintain and validate medical equipment and devices. * The above is not ... and regulatory guidelines as well as industry standards and best practices at all times. * All ...

Support the management team maintain and validate medical equipment and devices. * The above is not ... regulatory guidelines, as well as industry standards and best practices always. * All staff must ...