Medical Device Compliance Manager

Senior Quality Assurance Specialist for Medical DevicesMV | MysteryVibe is seeking an experienced Senior Quality Assurance Specialist to lead the development and implementation of Quality Management Systems (QMS) for ISO 13485 certification. This role requires close collaboration with product development and manufacturing teams to ensure alignment with...

Singular: Building Brilliant Biotechs is looking for a Medical Device Director to lead our regulatory affairs function. As a senior leader, you will define regulatory strategies, guide clinical and analytical validation studies, and liaise with regulatory authorities to ensure compliance with international medical device directives and regulations.The ideal...

About Us:We are a fast-growing medical device business committed to providing innovative solutions for women's and men's healthcare. Our mission is to make a significant impact on people's lives by developing clinically proven medical devices.To achieve this goal, we need a skilled professional to lead our quality assurance efforts and ensure compliance with...

Company OverviewMV | MysteryVibe is a leading innovator in women's and men's health devices. Our clinically proven medical devices adapt to the user's body, delivering targeted vibrations to address Genito-Pelvic pain, penetration pain, arousal disorder, and erectile dysfunction.We are committed to changing lives with our products, recommended by top doctors...

Job SummaryWe are seeking an experienced Biostatistics Lead - Medical Devices to join our team at Gb Tech. As a key member of our data analytics department, you will be responsible for leading the statistical analysis of clinical studies and ensuring high-quality data models.Key Responsibilities:Lead or contribute to the statistical analysis of clinical...

Company Overview:MV | MysteryVibe is an award-winning leader in women's & men's health devices. We create clinically proven medical devices that adapt to the user's body and deliver targeted vibrations to address Genito-Pelvic pain, penetration pain, arousal disorder & erectile dysfunction.The company has received recognition from leading doctors at Mayo...

We are looking for a Regulatory Compliance Specialist to join our team at MV | MysteryVibe, a company dedicated to improving women's and men's healthcare through clinically proven medical devices. The successful candidate will be responsible for creating and managing the necessary documentation and processes for ISO 13485 certification.About the RoleThis...

Key ResponsibilitiesAs our ideal candidate, you will have a strong background in IVD medical device product development and a deep understanding of global medical device directives.You will be responsible for leading our regulatory efforts, developing and implementing regulatory strategies to support new product development and commercialisation.You will...

Key ResponsibilitiesAs our new Head of Regulatory Affairs, you will define regulatory strategies, guide clinical and analytical validation studies, and liaise with regulatory authorities to ensure global commercial rollout of our revolutionary cancer diagnostic technology.You will provide strategic direction and operational oversight to the regulatory and...

Our client, a world-leading biotech company, is seeking an experienced Regulatory Compliance Specialist to join their team in Guildford. As a key leadership role, you will act as the Person Responsible for Regulatory Compliance (PRRC) for MDR/IVDR, ensuring the organisation meets all relevant regulatory standards across global markets.You will provide...

Sales Manager - Aesthetic DevicesHome Recruitment Ltd is a global leader in providing expert solutions to various industries. We are seeking an experienced Sales Manager to join our team in the South of the UK.About the Company:We specialise in supplying advanced FDA-approved skin rejuvenation devices, renowned for their outstanding treatment results. Our...

Role Overview:We are seeking a highly experienced Quality Assurance Specialist to join our team. As a key member of our organization, you will be responsible for developing and implementing our Quality Management System (QMS) and ensuring all documentation and processes are up-to-date.This role offers a unique opportunity to work closely with our product...

About the RoleWe are seeking an experienced Head of Regulatory Affairs to join Singular: Building Brilliant Biotechs' team in Guildford. As a key leadership figure, you will oversee regulatory compliance for MDR/IVDR, ensuring the organisation meets all relevant standards across global markets. You will provide strategic direction and operational oversight...

Cancer Diagnostic Innovation LeaderThe successful candidate will act as Person Responsible for Regulatory Compliance (PRRC) for MDR/IVDR, ensuring the organisation meets all relevant regulatory standards across global markets. They will provide strategic direction and operational oversight to the regulatory and quality teams, managing compliance with...

Opportunity OverviewWe are seeking a seasoned Regulatory Affairs Director to lead our team in Guildford. In this key role, you will be responsible for ensuring our organisation meets all relevant regulatory standards across global markets.This position requires strategic leadership and operational oversight to manage compliance with international medical...

About the JobAs a Device Inspection Specialist at Element Materials Technology, you will be responsible for preparing specimens for testing, performing tests as per customer specifications, and working under the supervision of senior technicians and/or Department Managers.Key Responsibilities:Gather and record test dataConstruct and maintain test fixtures...

About Building Brilliant BiotechsWe are a world-leading biotech company at the forefront of liquid biopsy technology, developing a patent-protected platform that captures rare circulating tumour cells (CTCs) from blood in a minimally invasive manner.Role OverviewWe seek an experienced Head of Regulatory Affairs to join our team in Guildford as Person...

MV | MysteryVibe is a small but fast-growing medical device business dedicated to improving women's and men's healthcare. We are seeking a Quality Management Systems Lead to join our team and lead the development and implementation of our QMS for ISO 13485 certification.About the JobThis role requires a strong understanding of quality management systems, ISO...

About Singular: Building Brilliant BiotechsWe are a world-leading biotech company at the forefront of liquid biopsy technology, capturing rare circulating tumour cells from blood in a minimally invasive manner. Our patent-protected platform pushes the boundaries of cancer diagnostics and personalised medicine.Job Title: Senior Regulatory Affairs Director for...

Lead Compliance Specialist for ISO 13485 CertificationWe are seeking a highly skilled Lead Compliance Specialist to join our team at MV | MysteryVibe. As a key member of our quality assurance department, you will be responsible for leading the development and implementation of Quality Management Systems (QMS) for ISO 13485 certification.This role requires...