Medical devices regulatory affairs jobs in MitchamCreate job alerts

Are you a detail-oriented professional with a strong background in quality assurance?. Training provider quality assurance:. Benefits – Senior Assurance Officer:.

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...

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). Our client, a global pharmaceutical company...

Training provider quality assurance:. Are you a detail-oriented professional with a strong background in quality assurance?. The Role – 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.

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 ...

Quality Assurance and Regulatory Affairs Lead Location: Hybrid - need to be able to attend the ... medical devices. * Proven experience in preparing and submitting regulatory filings, managing ...

... 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 ...

Reporting into the Director, Regulatory Affairs and Testing Duties will include: * Support ... Comprehensive medical, dental, vision, life insurance, and disability benefits (depending on ...

This role will support the Director for Regulatory Affairs and Testing in the production and uplift ... Comprehensive medical, dental, vision, life insurance, and disability benefits (depending on ...

... 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 ...