Latest Quality Assurance (MedTech) Jobs

Quality Engineer - Medical Devices - Oxford

Quality Engineer - Medical Devices - OxfordThere is an excellent opportunity for a Quality Engineer to join a growing and innovative medical devices team in Oxford. Newton Colmore is recruiting for this position exclusively, meaning applications must be made directly through us to be considered.We are seeking someone with a...

Newton Colmore

Oxford

QA Intern: Medical Devices, Impactful Projects & Growth

A leading healthcare company is seeking an Intern for their Technical Quality Assurance team in Witney. The role involves collaborating on product development, supporting design transfers, and maintaining quality standards. Candidates should be pursuing a degree in relevant fields such as engineering or chemistry and must be proactive and organized....

Abbott Laboratories

Witney

Senior Manager, Quality Assurance & Regulatory Affairs- UKI & Nordics

Senior Manager, Quality Assurance & Regulatory Affairs – UKI & Nordics 3 days ago – Be among the first 25 applicants. Job Description Summary The Senior Manager QRA UKI and Nordics leads the Quality Assurance and Regulatory Affairs function across the region, ensuring full compliance with internal standards and external...

BD (Tissuemed Ltd)

Winnersh

Quality Engineer - Cambridge - Medical Devices)

Quality Engineer - Cambridge - Medical Devices We are currently looking for a Quality Engineer for a growing Medical Devices organisation based in Cambridge. The company works on a range of different Medical Devices, providing a variety of projects and tasks in your role. You will collaborate with various Medical...

Newton Colmore Consulting

Cambridge

Quality Engineer - Medical Devices - Oxford)

Quality Engineer - Medical Devices - Oxford There is an excellent opportunity for a Quality Engineer to join a growing and innovative medical devices team in Oxford. Newton Colmore is recruiting for this position exclusively, meaning applications must be made directly through us to be considered. We are seeking someone...

Newton Colmore Consulting

Oxford

Quality Engineer, Medical Devices – ISO 13485 & CAPA Expert

A recruitment agency is seeking a Quality Engineer for a position in Oxford. The role involves contributing to the development of a transformative medical device, requiring expertise in ISO 13485 and experience with electro-medical devices. The ideal candidate will join an established Quality Assurance team with responsibilities including managing CAPA...

Newton Colmore

Oxford

Quality Engineer

Location: Nottinghamshire - Onsite  Are you a detail-driven Quality Engineer who loves improving processes, strengthening systems and making a genuine impact on product excellence?  If you thrive in a fast-paced technical environment and want a desk-based role where your engineering mind really gets to shine, this could be your next...

Precept Recruit

Bilborough

Quality Officer

Bertelsmann is a media, services and education company that operates in about 50 countries around the world. It includes the broadcaster RTL Group, the trade book publisher Penguin Random House, the magazine publisher Gruner + Jahr, the music company BMG, the service provider Arvato, the Bertelsmann Printing Group, the Bertelsmann...

Arvato SCM UK Ltd

Lockington, Leicestershire

Quality Engineer

Location: Newark - Onsite Are you a detail-driven Quality Engineer who loves improving processes, strengthening systems and making a genuine impact on product excellence?  If you thrive in a fast-paced technical environment and want a desk-based role where your engineering mind really gets to shine, this could be your next...

Precept Recruit

Southwell

Product Quality Engineer - Medical Devices

OverviewProduct Quality Engineer – Medical DevicesLocation: KidlingtonSalary: Highly Negotiable, Dependent on ExperienceAn exciting opportunity to join a growing medical imaging company developing cutting-edge 3D imaging technology. With commercialisation underway in the UK and US, we are expanding our manufacturing capability and seeking a Product Quality Engineer to strengthen the Quality...

CT19

Kidlington

Senior Quality Engineer - Cambridge - Medical Devices)

Senior Quality Engineer - Cambridge - Medical Devices We are currently looking for a Senior Quality Engineer for a growing Medical Devices organisation based in Cambridge. The company work on a range of different Medical Devices, providing a variety of projects and tasks in your role. You will collaborate various...

Newton Colmore Consulting

Cambridge

Onsite Quality Engineer - MedTech, ISO CFR820, CI

Job Description SummaryWe have an exciting new opportunity to recruit an experienced quality engineer to join our quality engineers within the plant of 800 + employees. In this onsite role, you will oversee all operational aspects of the quality system, enhance operational efficiency on the manufacturing floor, manage non-conforming materials,...

BD

Plymouth

Clinical Trials QA & Regulatory Lead

A leading educational institution is seeking a Regulatory and Governance Affairs Officer for the Quality Assurance department. You will oversee compliance in clinical trials, manage a quality assurance team, and work closely with stakeholders. Candidates should have substantial clinical trials management experience and excellent communication skills. The role includes competitive...

University of Leeds

Leeds

Senior Regulatory Affairs & QA Lead - Medical Devices

A healthcare company based in Corsham is seeking a Senior Regulatory Affairs and Quality Assurance Specialist to support quality compliance within the medical device industry. The role involves leading a team to ensure QMS effectiveness, contributing to regulatory submissions, and ensuring adherence to international regulations. Candidates should possess a relevant...

TipTopJob

Corsham

QARA Administrator

QARA AdministratorSalary £28k- £30k per annumDetailsJob Summary:The QARA Administrator supports the Quality Assurance (QA) and Regulatory Affairs (RA) functions to ensure the Planer's medical devices comply with applicable regulatory requirements (e.g., ISO 13485, MDR 2017/745, FDA 21 CFR 820). This role plays a key part in maintaining documentation, coordinating quality...

Proactive Global

Sunbury Common