Medical devices regulatory affairs jobs in IsleworthCreate job alerts

We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. Planet Pharma are partnered with a leading biotechnology company and we are actively seeking a Senior ...

As a Quality Assurance Officer at Taiko Foods, you will be responsible for ensuring that all products meet the highest standards of quality and safety. Check products against factory product specifications to ensure compliance with specifications, legality, and consistency in quality and report a...

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...

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...

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.

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.

In order to make an application, simply read through the following job description and make sure to attach relevant documents.The Education Quality Assurance (EQA) Team ensures all providers of professional education and training for nurses, midwives and nursing associates continue to meet the re...

... 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 ...

Extensive experience in global regulatory affairs within the pharmaceutical, biotech, medical device industry ideally within a dynamic, fast-moving environment. * Extensive knowledge of preparing and ...

... 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 ...

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 ...

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