regulatory quality officer jobs in Devon

Senior Systems & Regulatory Software Engineer Medical Devices | High Salary or High-Rate Contract | Kent | Remote We are seeking an experienced Technical Expert to join our global team, working with active medical devices under MDR 2017/745 and ISO 13485 standards Electrionics device and audit experience is recognised. This is a fully remote role, offering the flexibility to work from...

Head Regulatory AI / Software as a Medical Device (SaMD) UK-based | Remote A high-growth healthcare Digital Health company with large-scale real-world deployments across the UK and US is hiring a Head of Regulatory to lead global regulatory and quality strategy. The Role You’ll own the global regulatory roadmap across UK, EU, US and emerging markets, combining strategic leadership with...

We’re recruiting for a GPhC registered Pharmacist with UK manufacturing and/or production experience to take ownership of operational quality and formulation strategy in a regulated pharmaceutical environment. We welcome applications from candidates with relevant expertise from the pharma industry, regulatory bodies and the NHS. To be considered for the role you must currently be based in the...

Job Description Quality Technician – Documentation & Compliance Role Summary The Quality Technician – Documentation & Compliance supports manufacturing operations by developing, maintaining, and improving quality documentation and compliance processes. The role focuses on SOPs, work instructions, training records, and internal audits to ensure consistency and adherence to quality and...

An opportunity has opened for a Quality Manager to join a regulated manufacturing site in Ashington. This role offers real ownership of quality systems, audits, and continuous improvement, making it ideal for someone ready to step into a visible and influential position. Whats in it for you - Annual bonus scheme - Private medical insurance - Enhanced pension contributions - 25 days holiday plus...

You will lead quality assurance and quality control activities, helping ensure products consistently meet customer requirements, regulatory obligations, and internal quality standards.

You will lead core GCP quality activities including quality system oversight, audit planning and execution, and regulatory inspection readiness. This role offers the opportunity to influence quality strategy, shape inspection preparedness, and drive continuous improvement across a growing clinical portfolio.

We’re hiring a Senior Quality Assurance Specialist known as a Quality Senior Scientist internally Location: Chippenham, Wiltshire, 2 days a week hybrid Contract: Fixed-Term Contract (12 months) Reports to: Scientific Affairs Director – Pharma Division Are you passionate about driving quality excellence in healthcare? Do you thrive in a regulated environment where your expertise directly...

You will act as an external arm of their clients, liaising with and managing CDMO's, and other key Vendors.

You will be speaking with key stakeholders including C-suite, and VP level, as well as connecting with entry level and specialists within their clients.

Senior Quality Engineer Medical Device Startup | £60M Raised Why This Role Matters This is a rare opportunity to join a high-growth medical device startup that has raised £60M from top-tier investors and is scaling rapidly towards global commercialisation. The company is building next-generation medical technologies that will meaningfully improve patient outcomes. As Senior Quality Engineer,...

Job Description As a Regulatory Officer, you'll play a vital role in shaping the future of recycling in England and see the impact of your work every day. Working within our Combined Packaging Regime team in Waste Markets & Shipments (WM&S), you'll help reduce waste, improve recycling standards, and support businesses to operate more sustainably. You'll regulate producers who place packaging on...

Role Overview Our client, a pioneering company in the medical technology industry, is seeking a Quality Validation Manager to join their team. This role is based in the UK and offers the unique chance to work remotely, with occasional trips to the company’s headquarters. As the Quality Validation Manager, you will play a crucial role in the development and validation of their unique...

Head Regulatory AI / Software as a Medical Device (SaMD) UK-based | Remote A high-growth healthcare Digital Health company with large-scale real-world deployments across the UK and US is hiring a Head of Regulatory to lead global regulatory and quality strategy. The Role You’ll own the global regulatory roadmap across UK, EU, US and emerging markets, combining strategic leadership with...

Senior Systems & Regulatory Software Engineer Medical Devices | High Salary or High-Rate Contract | Kent | Remote We are seeking an experienced Technical Expert to join our global team, working with active medical devices under MDR 2017/745 and ISO 13485 standards Electrionics device and audit experience is recognised. This is a fully remote role, offering the flexibility to work from...

Role Overview Our client, a pioneering company in the medical technology industry, is seeking a Quality Validation Manager to join their team. This role is based in the UK and offers the unique chance to work remotely, with occasional trips to the company’s headquarters. As the Quality Validation Manager, you will play a crucial role in the development and validation of their unique...

We’re hiring a Senior Quality Assurance Specialist known as a Quality Senior Scientist internally Location: Chippenham, Wiltshire, 2 days a week hybrid Contract: Fixed-Term Contract (12 months) Reports to: Scientific Affairs Director – Pharma Division Are you passionate about driving quality excellence in healthcare? Do you thrive in a regulated environment where your expertise directly...

Quality Technician – Documentation & Compliance If you want to know about the requirements for this role, read on for all the relevant information. Role Summary The Quality Technician – Documentation & Compliance supports manufacturing operations by developing, maintaining, and improving quality documentation and compliance processes. The role focuses on SOPs, work instructions, training...

You will lead core GCP quality activities including quality system oversight, audit planning and execution, and regulatory inspection readiness. This role offers the opportunity to influence quality strategy, shape inspection preparedness, and drive continuous improvement across a growing clinical portfolio.

Quality Technician - Documentation & ComplianceRole SummaryThe Quality Technician - Documentation & Compliance supports manufacturing operations by developing, maintaining, and improving quality documentation and compliance processes. The role focuses on SOPs, work instructions, training records, and internal audits to ensure consistency and adherence to quality and regulatory standards.This is...

Quality Technician – Documentation & Compliance Role Summary The Quality Technician – Documentation & Compliance supports manufacturing operations by developing, maintaining, and improving quality documentation and compliance processes. The role focuses on SOPs, work instructions, training records, and internal audits to ensure consistency and adherence to quality and regulatory...