Quality Assurance Manager for Medical Devices

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...

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...

Regulatory Compliance SpecialistSingular is looking for a highly skilled Medical Device Compliance Manager to oversee regulatory compliance across the organisation.Estimated Salary: £95,000 - £130,000 per annumAbout the TeamThe regulatory and quality teams work closely together to ensure the organisation meets all relevant regulatory standards.The team...

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...

Job SummaryWe are seeking a highly experienced Medical Device Compliance Manager to join our team in Guildford. This is an exciting opportunity to lead our regulatory efforts and ensure compliance with global medical device regulations.In this role, you will be responsible for developing and implementing regulatory strategies to support new product...

We are seeking a highly skilled Senior Quality Assurance Specialist to join our team at MV | MysteryVibe. In this exciting role, you will be responsible for leading the development and implementation of our Quality Management System (QMS) for ISO 13485 certification.As a Senior Quality Assurance Specialist, you will create and manage technical files, SOPs,...

Singular: Building Brilliant BiotechsJob DescriptionWe are looking for a skilled Medical Device Compliance Specialist to lead our regulatory affairs team. As the Head of Regulatory Affairs, you will be responsible for ensuring our organisation's products meet the required regulatory standards worldwide.Key responsibilities include providing strategic...

About the OpportunitySingular: Building Brilliant Biotechs is seeking an experienced Head of Regulatory Affairs to join its team in Guildford. As a key member of the team, you will be responsible for ensuring the organisation meets all relevant regulatory standards across global markets. You will provide strategic direction and operational oversight to the...

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...

Singular: Building Brilliant BiotechsOpportunity OverviewWe are seeking a highly experienced Regulatory Affairs Director to join our team in Guildford. This senior leadership role involves overseeing our regulatory affairs strategy, ensuring our organisation meets all relevant regulatory standards across global markets.You will lead the regulatory and...

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...

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...

ISO 13485 Quality Assurance LeadWe are seeking an experienced ISO 13485 Quality Assurance Lead to join our quality assurance department at MV | MysteryVibe. As a key member of our team, you will be responsible for leading the development and implementation of Quality Management Systems (QMS) for ISO 13485 certification.This role requires close collaboration...

We are looking for a highly skilled Quality Assurance Engineer to join our team at Element Materials Technology in Surrey Hills, Guildford.This is a challenging role that involves preparing material specimens for testing, performing tests as directed by customer specifications, and gathering and recording test data.As a Quality Assurance Engineer, you will...

We are looking for a Quality Assurance Manager for Medical Devices to join our team at MV | MysteryVibe. As a Quality Assurance Manager, you will oversee the development and implementation of our Quality Management System (QMS) for ISO 13485 certification.You will be responsible for creating and managing technical files, SOPs, risk management reports, and...

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...

Job Opportunity: Medical Screening ProfessionalWe are seeking an experienced Medical Screening Professional to join our team in the Guildford area. As a Medical Screening Professional, you will be responsible for conducting health surveillance screening, recording medical information, and supporting health promotion activities. This is a full-time position...

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...

Are you looking for a challenging and rewarding role as an Occupational Health Technician?About the Opportunity:This position involves working with a leading occupational health provider in the Guildford area, conducting health surveillance screenings, and ensuring accurate recording of medical information.Key Tasks:Conduct health surveillance...

About ErgomedErgomed is a mid-sized pharmacovigilance service provider established in 2008. We have achieved global organic growth year after year, with staff based across Europe, North America and Asia, covering services within Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.We provide first-class support to our small to...