Medical Device Compliance Officer

GS Medical: Delivering Quality Medical Device SolutionsAs a leading provider of medical device solutions, we serve hospital customers in Ireland and the UK with our comprehensive range of services.We pride ourselves on our global market knowledge, expert staff, and commitment to delivering exceptional results.The RoleWe are seeking a skilled Service Engineer...

About GS Medical LimitedWe provide comprehensive Medical Device Solutions to hospitals in Ireland and the UK. With facilities in Dublin and the UK, we offer expert knowledge, broad expertise, and flexible delivery options.The PositionWe are looking for a dedicated Junior Service Engineer to join our team.This field-based role requires performing validation,...

About the RoleWe are seeking an experienced Regulatory Compliance Specialist to join our team. The successful candidate will be responsible for overseeing regulatory compliance for medical products procured, stored, transported, and sold by all companies operating in Ireland, UK, and Switzerland.Main AccountabilitiesOversee regulatory compliance for medical...

This is an excellent opportunity for a Medical Device Specialist to join our team and contribute to the success of our clients. As a Regulatory Compliance Officer, you will be responsible for ensuring that medical products meet regulatory requirements, providing advice on new legislation, and coordinating product compliance data collection and assessment.Key...

Medical Device Specialist Job SummaryWe are seeking an experienced Medical Device Specialist to join our team at TN Ireland. The successful candidate will be responsible for managing the implementation of medical devices, ensuring compliance with regulatory requirements, and maintaining high levels of customer satisfaction.About the RoleThe Medical Device...

Job TitleMedical Device InspectorJob SummaryWe are seeking a highly skilled Medical Device Inspector to join our team at TN Ireland. As a key member of our quality assurance department, you will be responsible for ensuring the quality and integrity of our medical devices.About the RoleThe successful candidate will have a Bachelor's Degree in a related field...

We are seeking a detail-oriented and organized Global Regulatory Coordinator to join our team at Teleflex. In this role, you will be responsible for supporting the regulatory activities of our company in the EMEA region.Key ResponsibilitiesRegulatory Support: Assist in the development and implementation of regulatory strategies to ensure compliance with...

The Senior Quality Engineer will be responsible for ensuring the highest standards of quality throughout the product development process. This includes developing quality plans, conducting quality reviews, and providing recommendations for improvement.Key Skills:Bachelor's degree in a relevant Engineering or Science field.4-5 years' experience in the medical...

Job Description: We are currently recruiting for a Medical Device Manager to oversee the development and implementation of innovative medical devices. This role requires both technical expertise and a strong understanding of quality and regulatory standards within the medical device industry.Responsibilities: Develop and execute strategies to drive medical...

The role of Regulatory Compliance Officer involves overseeing the regulatory compliance for medical products procured, stored, transported and sold by companies operating in Ireland, UK, and Switzerland. The successful candidate will also provide advice on new legislation and business needs, control company registrations with regulators, and coordinate...

Job DescriptionWe are seeking a Regulatory Compliance Officer to join our team at TN Ireland. The successful candidate will be responsible for ensuring that our medical device studies comply with all relevant regulatory requirements.About the RoleThe Regulatory Compliance Officer will be responsible for maintaining appropriate regulatory documents, reporting...

Key AccountabilitiesThe successful candidate will have the following key accountabilities:Regulatory Compliance:• Ensure full compliance with the Medical Device Regulations (MDR) in your capacity as PRRC for the European Authorized Representative.• Lead communications and interactions with Competent Authorities regarding Vectura's duties as Authorized...

This permanent hybrid role based in Dublin HQ offers a unique opportunity to join a young and exciting clinical-stage biotechnology company focused on discovering and developing novel therapies for debilitating diseases. As a Senior Director Regulatory Affairs Device, you will lead key elements of regulatory systems, ensuring compliance with relevant...

About Us:Vectura Group is a global leader in the development and delivery of inhaled medicines and medical devices. We are dedicated to innovation, quality, and compliance in delivering effective treatments for patients worldwide.Job Summary:We are seeking an experienced Manager - Regulatory Affairs and Medical Devices to contribute to our regulatory affairs...

Company OverviewCPL is a leading provider of scientific services, including research and development, manufacturing, and regulatory affairs. We specialize in the development of medical devices and pharmaceuticals, working closely with clients to deliver innovative solutions that meet their unique needs. Our team of experts has extensive experience in product...

Job Title: Senior Manager Regulatory Affairs for Medical Devices\Vectura Ireland Limited is seeking a Senior Manager in Regulatory Affairs for Medical Devices who will also assume the critical role of Person Responsible for Regulatory Compliance (PRRC). This position plays a key role in ensuring compliance with European medical device regulations as...

Job DescriptionVectura Group plc is seeking a highly experienced Senior Manager in Regulatory Affairs for Medical Devices to assume the critical role of Person Responsible for Regulatory Compliance (PRRC) as EU Authorized Representative.This position plays a key role in ensuring compliance with European medical device regulations. The successful candidate...

Job DescriptionAs a Product Development Engineer at CPL, you will be responsible for designing, developing, and optimizing medical devices aimed at improving the lives of individuals with tinnitus. Your primary focus will be on leading product development activities from design and prototyping to testing, validation, and commercialization. This role requires...

As a Senior Director Regulatory Affairs Device, you will be responsible for leading key elements of regulatory systems, ensuring compliance with relevant standards for medical devices including ISO 13485 and FDA QSR. This role involves defining the device regulatory strategy and overseeing all device submissions across global markets.Job Description:You will...

**Job Description:**We are seeking a QC Compliance Officer to join our team at Quanta Consultancy Services Ltd. As a key member of our Quality Team, you will be responsible for ensuring that our organisation complies with all relevant regulations and guidelines.**Key Responsibilities:**Assure that all product complaints are investigated to the appropriate...