Regulatory Medical Experts

ResponsibilitiesAs a Medical Device Regulatory Expert, you will play a critical role in ensuring that our products comply with regulatory requirements. You will have a deep understanding of regulatory frameworks, including ISO 13485 and 21 CFR Part 820, and be able to interpret and apply these regulations to our products.You will work closely with our...

About the Company:The Medical Council is a professional regulatory body responsible for protecting the public by promoting high standards of medical education and training.We are seeking an experienced solicitor to join our Legal Services Team as a Regulatory Solicitor (Assistant Principal Grade).

About the RoleWe are seeking a Senior Medical Physics Expert to provide scientific and technical support to several major teaching hospitals in Ireland. This position requires strong collaboration with healthcare professionals, ensuring that physics-related activities meet the highest standards of safety, quality, and cost-effectiveness.The successful...

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...

Job Requirements:We are seeking a highly skilled Regulatory Compliance Expert to join our team in Europe. As a Regulatory Compliance Expert, you will be responsible for ensuring compliance with all relevant standards and legislative requirements pertinent to EU regulations.About the Role:This is a pivotal leadership role that requires proven quality...

About the CompanyBausch + Lomb is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world. We offer a comprehensive portfolio of over 400 products that meet the diverse needs of customers across the globe. Our mission is to help people see better, to live better.About the JobWe are...

Company Overview:">AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services...

**Job Overview**BCL Legal, a well-regarded law firm, is seeking an experienced Defendant Clinical Negligence Associate to join its team. As a key member of the practice group, you will work alongside a highly respected Partner acting for insurers and indemnity providers for medical professionals.The opportunity revolves around representing a range of...

We are seeking a highly skilled and proactive Biotechnology Regulatory Expert to join our team at TN Ireland.The successful candidate will be responsible for identifying business-critical aspects of regulatory intelligence information and communicating effectively to internal/external stakeholders as applicable.This role requires a solid understanding of the...

We are a global leader in medical technologies, dedicated to improving healthcare outcomes through innovative solutions. As a Regulatory Affairs specialist at Teleflex, you will play a vital role in ensuring the compliance of our medical products in the EMEA region.About the TeamWe pride ourselves on our collaborative environment, where diversity and...

We're seeking a highly skilled Medical Director to lead our clinical trials team. This role requires expertise in medical monitoring, safety assessment, and regulatory compliance. As the primary medical expert, you'll oversee the execution of clinical trial protocols, ensuring accuracy, integrity, and successful outcomes.The ideal candidate will have...

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...

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...

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...

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,...

Job Title: Regulatory Affairs ExpertCompany OverviewAt TN Ireland, we are a well-established international healthcare business with a significant presence in Ireland, the UK, and mainland Europe.We have a new opportunity for a Regulatory Affairs Expert to join our team in Tullamore, Co Offaly.

Amicus Search & Recruitment is expanding its Regulatory & Information team, seeking a seasoned Regulatory Law Expert to join their dynamic practice in Dublin. As a key member of the team, you will provide expert advice on contentious and non-contentious regulatory matters, including food law, health and safety, consumer law, State aid, and information...

At ProPharma, we are committed to improving the health and wellness of patients by providing expert advice and consulting services to biotech, med device, and pharmaceutical organizations.We are looking for an experienced Medical Writer to join our team and support our global growth. This is a fully remote role across any of our ProPharma entities.The ideal...

Job DescriptionKey ResponsibilitiesDevelop and implement regulatory strategies for new and modified products/product families.Prepare and execute regulatory filings such as technical files, Canadian submissions, and letters to file.Conduct international registrations in accordance with and in support of regulatory strategies.Provide input on and approve...

Company Overview:Syneos Health, Inc. is a leading biopharmaceutical solutions organization dedicated to accelerating customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes that address modern market realities.Job Description:This role offers an exciting opportunity to join our team as a Regulatory Medical...