Medical devices regulatory affairs jobs in RichmondCreate job alerts

Regulatory Director - Complex Software/Electronic Medical Devices. Solid experience within medical device regulatory affairs. Proven experience of successful submission of complex Class IIb/III active medical devices in China or Russia.

Are you a detail-oriented professional with a strong background in quality assurance?.Benefits – Senior Assurance Officer:.Full time, 35 hours per week, 9am-5pm Monday-Thursday with 45 minutes lunch, 9am-4pm Friday with 1 hour lunch.Hybrid working (office in London).Significant investment in empl...

The Education Quality Assurance (EQA) Team ensures all providers of professional education and training for nurses, midwives and nursing associates continue to meet the required standards, in accordance with the Councils statutory duties.

Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory guidance across the EU region and make sure that regulatory deadlines and approvals are achieved (previous EU exposure is preferred). Acting as a point of contact between the co...

The Education Quality Assurance (EQA) Team ensures all providers of professional education and training for nurses, midwives and nursing associates continue to meet the required standards, in accordance with the Councils statutory duties. About the RoleThis role will ensure the safe and effective...

Senior Regulatory Affairs Associate / Regulatory Affairs Manager EU contract jobYour new companyThis global biopharmaceutical company is looking for an experienced Regulatory Affairs professional to join them on a contract basis, 12 month, hybrid contract job with scope for extension Your new rol...

To apply – Senior Assurance Officer:. Benefits – Senior Assurance Officer:. About the Organisation – Senior Assurance Officer:.

Description About the TeamThe Education Quality Assurance (EQA) Team ensures all providers of professional education and training for nurses, midwives and nursing associates continue to meet the required standards, in accordance with the Councils statutory duties.

Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory guidance across the EU region and make sure that regulatory deadlines and approvals are achieved (previous EU exposure is preferred). Acting as a point of contact between the co...

Hobson Prior is seeking a Regulatory Affairs Specialist for a Senior position to oversee the ... Prepare and submit regulatory applications for drugs, cosmetics, medical devices, and food ...

... 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 ...

... 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 ...

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 ...

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 ...

Demonstrable success in selling medical devices or service contracts to the NHS and/or private healthcare providers. * Strong knowledge of procurement processes and regulations within the healthcare ...

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