Medical devices regulatory affairs jobs in MordenCreate job alerts

Senior Regulatory Affairs Associate. As part of their growth, they are searching for an experienced regulatory professional with relevant medical device or similar experience. Their Regulatory Affairs Team underpin the whole business.

Annual discretionary bonus subject to business and overall performanceDiscretionary Life AssuranceDiscretionary Income ProtectionGroup Personal PensionPrivate Medical Cash Pla.

Established in 1997 as the first manufacturer of sushi for the UK supermarket industry, Taiko has evolved into the most innovative manufacturer of Sushi, Food To Go, Prepared Meals and Snacking products in the UK, supplying Waitrose, Tesco and Sainsbury’s to name a few.Over the past 25 years Taik...

This is a permanent position working Monday to Friday 9am-6pm offering a salary of £27,500 per annum plus excellent benefits!As Quality Assurance Officer you will be working in a quality team of 5, assisting in the operational performance of the Quality Assurance (QA) function, ensuring the succe...

Module 3 IND, IMPD, amendments and annual reports) for assigned BicycleTx programs or projectsDeveloping and maintaining internal cross-functional relationships to support the development and execution of CMC regulatory submissions for assigned BicycleTx programs or projectsMay act as the Global/...

As Quality Assurance Officer you will be working in a quality team of 5, assisting in the operational performance of the Quality Assurance (QA) function, ensuring the successful delivery of business strategies and objectives, whilst adhering to regulatory compliance and achieving commercial succe...

Minimum five years of experience in Regulatory Affairs related to medical devices, drugs and/or biologics, developing regulatory deliverables and submissions. The primary roles and responsibilities include writing, reviewing, and managing regulatory submissions, development of overall regulatory ...

We are currently recruiting for a Quality Assurance Officer to join a leading pharmaceutical manufacturer based in West Molesey.This is a permanent position working Monday to Friday 9am-6pm offering a salary of £27,500 per annum plus excellent benefits!.Scroll down for a complete overview of what...

We are currently recruiting for a Quality Assurance Officer to join a leading pharmaceutical manufacturer based in West Molesey.This is a permanent position working Monday to Friday 9am-6pm offering a salary of £27,500 per annum plus excellent benefits!.Scroll down for a complete overview of what...

... for a Regulatory Affairs Manager to support their growing business. They are looking for an ... regulatory documents for medical devices and pharmaceuticals. * Working with Notified Bodies ...

Key Responsibilities * Assist in securing regulatory approvals for new and existing medical devices ... Additional training or certifications in Regulatory Affairs or Medical Devices Benefits

Job Title: Medical Affairs Associate Location: London, UK About the Role: As a Medical Affairs ... Familiarity with regulations and scientific education best practices. Behavioural Competencies

Knowledge of EU MDR 2017/745 for Medical Devices (Class I, Is and IIa), and Regulation (EU) 2016 ... Report on the Regulatory Affairs aspects and any need for improvements. Quality * Help the Dept. in ...

The ideal candidate will possess a robust background in Quality & Regulatory affairs and excel in a ... of medical devices * Evaluate and authorize project documentation as needed * Assist in ...

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 ...

Head of Medical Writing and Regulatory Affairs The Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will ...

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 ...

Knowledge of Medical Affairs, Clinical Development, and Regulatory functions. * Familiarity with relevant guidelines (GPP3, ICMJE), laws, and industry best practices. * Proficiency with Microsoft ...

Regulatory Affairs Coordination : Ensure market access strategies are compliant with relevant ... Work closely with internal teams (Sales, Marketing, Medical Affairs, Clinical, etc.) to ensure ...

... to their Medical Affairs team on basis. Hybrid role - 3 days per week in the office Role ... Ensure all company SOPs and UK regulatory guidelines are followed * Ensure smooth cross-functional ...

Demonstrable experience in the field of government and regulatory affairs and with ... disability, medical condition, marital status, genetics, age, or veteran status or any other ...

Prior experience in the field of government and regulatory affairs and with telecommunications ... disability, medical condition, marital status, genetics, age, or veteran status or any other ...

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