Device Regulatory Expert

Job Description: Quality Assurance and Regulatory Affairs ExpertCompany Overview:Newton Colmore Consulting is a leading consulting firm in the medical devices industry, providing expert advice on regulatory affairs and quality assurance. We are committed to delivering high-quality services that meet the needs of our clients, and we are seeking a talented...

Cpl Life Sciences is seeking a highly experienced Medical Device Development Expert to join our team in Cambridge. The ideal candidate will have a strong background in drug delivery device development and testing, with excellent knowledge of design control systems and mechanical/electronic testing.Key Responsibilities:• Work closely with multidisciplinary...

We are looking for an experienced Device Development Expert with a strong background in drug delivery devices to join our team at Cpl Life Sciences. As a key member of our multidisciplinary team, you will be responsible for working closely with designers, mechanical engineers, quality specialists, and regulatory experts to develop and deliver innovative drug...

Regulatory Affairs Manager for Medical Devices and Combination ProductsVectura Group is a global leader in developing innovative inhaled therapies and drug-device combination products (DDCPs). We are seeking a skilled and motivated Regulatory Affairs Manager to join our team and help drive the success of our medical device and DDCP regulatory...

Role Overview: Medical Device Compliance SpecialistAbout Us:Newton Colmore Consulting is a leading consulting firm in the medical devices industry, providing expert advice on regulatory affairs and quality assurance. Our mission is to deliver high-quality services that meet the needs of our clients, and we are seeking a talented individual to join our team...

About the RoleSagentia Innovation is seeking a skilled Regulatory Affairs Specialist to support our Human Factors compliance offering within the Medical Sector. As a key member of our team, you will work closely with our Head of Human Factors to develop and implement Human Factors/Usability Engineering Files and use-related risk documentation, ensuring best...

We are 52North, creators of Neutrocheck®, a med-tech company striving to transform patient experiences and set new industry standards through innovative technology.This exciting opportunity requires a Regulatory Compliance Expert to oversee our QMS, ensure adherence to regulations, and develop effective quality processes.ResponsibilitiesLeading the...

Reed Scientific, a leading partner in the biotech industry, is seeking an experienced Regulatory Affairs Specialist to join their team. This exciting opportunity will see you play a crucial role in ensuring the quality and regulatory compliance of innovative medical devices.  About the Role:This key position will require you to maintain and improve robust...

About the RoleWe are seeking a talented Device Development Scientist to join our team at SRG. As a key member of our multidisciplinary team, you will work closely with design, mechanical, quality, compliance regulatory, human factors, and formulation engineers and scientists to develop and test drug delivery devices.Key ResponsibilitiesCollaborate with...

**Newton Colmore Consulting: A Specialist Recruitment Company in the Medical Devices Sector**We are currently seeking a highly skilled Medical Devices Mechanical Engineer to join our team. Based in South Cambridgeshire, this role will involve utilizing SolidWorks for the CAD design of new Medical Devices.The ideal candidate will have a strong background in...

Cambridge-Based Design and Medical Devices Expert SoughtWe are seeking an exceptional Design and Medical Devices expert to join our R&D team in Cambridge. The successful candidate will have experience in the Medical Devices sector, with a strong understanding of human factors and user-centered design principles.This role involves working closely with...

Job Description: We are seeking a Quality Assurance Specialist to assist in the development of our QMS system for ISO 13485 standards.This role involves creating and managing technical files for several Medical Devices lines, including Class I, Class IIa and Class IIb Medical Devices.You will collaborate with Medical Devices experts and be responsible for...

We are MoonLake Immunotherapeutics, a biotech company that aims to transform global healthcare with novel therapies. We offer an exciting opportunity for a Technical Lead for Device Development to join our team.Job DescriptionThe Senior Technical Manager, Device will act as the subject matter expert responsible for all activities related to the development...

About the RoleVectura Group is a global leader in developing innovative inhaled therapies and drug-device combination products. We are seeking a highly experienced Medical Device Compliance Manager to join our regulatory affairs team.Key Responsibilities:Assume the role of Regulatory Affairs Manager with specialized expertise in medical devices and...

Are you a talented Electronics Design Engineer looking for a new challenge? We are seeking a Medical Devices Electronics Design Expert to join our team in Cambridge.Job SummaryAs a Medical Devices Electronics Design Expert, you will be responsible for designing and developing new medical devices. You will work closely with cross-functional teams to ensure...

Job OverviewNewton Colmore Consulting Ltd is a leading recruitment agency in the biotech and medical devices sectors, seeking an experienced Senior Software Development Engineer to join their team.This role offers an exciting opportunity to work with electro-mechanical devices used in biotech and medical devices, contributing to the development of...

Role OverviewWe are seeking a highly skilled Senior Neurotechnology Device Development Director to lead our neurotechnology devices development team at Vector Recruitment Ltd.About the RoleThis is an exceptional opportunity for a senior leader with experience in developing complex implantable medical devices. As a key figure in our Neurotech department, you...

Regulatory LeadershipVectura Group, a global leader in inhaled therapies and drug-device combination products, seeks a seasoned Regulatory Affairs Manager to drive the success of our medical device and DDCP regulatory activities.Regulatory Expertise: Lead regulatory activities across Vectura Group, specializing in medical devices and DDCPs, to support...

Job SummaryWe are seeking a skilled Regulatory Affairs Specialist to join our team at Vectura Group. As a key member of our regulatory affairs department, you will play a crucial role in ensuring compliance with global regulations and guidelines for medical devices and drug-device combination products.Key Responsibilities:Lead regulatory activities across...

About This RoleWe are seeking an experienced Senior Human Factors Engineer to join our team at Newton Colmore Consulting Ltd. As a key member of our medical devices practice, you will work closely with world-class engineers, surgeons, nurses, and healthcare professionals to ensure the usability of medical devices.Key ResponsibilitiesApply human factors...