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📑 IVD Regulatory Affairs Specialist | Remote | EU Proclinical are seeking a dedicated professional to lead regulatory affairs in the in-vitro diagnostics sector within the EU for a Regulatory Specialist role which is a remote position. Responsibilities: - Independently assemble and maintain technical and regulatory documentation for EU Annex XIV ...

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📑 The Role As the Regulatory Affairs Specialist, you will be responsible for; Creating technical files for a range of medical devices, both new and existing devices Perform gap analysis and revision of existing documentation to ensure compliance with MDR Respond to and internal or external regulatory affairs queries You As the Regul ...

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📑 IVD Regulatory Affairs Specialist | Remote | EU Proclinical are seeking a dedicated professional to lead regulatory affairs in the in-vitro diagnostics sector within the EU for a Regulatory Specialist role which is a remote position. Responsibilities: - Independently assemble and maintain technical and regulatory docume ...

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📑 The Role As the Regulatory Affairs Specialist, you will be responsible for; Creating technical files for a range of medical devices, both new and existing devices Perform gap analysis and revision of existing documentation to ensure compliance with MDR Respond to and internal or external ...

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📑 Senior Regulatory Affairs Specialist Corinium Centre, Love Lane Industrial Estate, Cirencester GL7 1YJ, UK Req #233 04 April 2024 Corin is seeking a Senior Regulatory Affairs Specialist to be responsible for product registration and all regulatory aspects of post-market surveillance. The Regulatory Affairs Specialist will require knowledge o ...

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📑 Senior Regulatory Affairs Specialist Corinium Centre, Love Lane Industrial Estate, Cirencester GL7 1YJ, UK Req #233 04 April 2024 Corin is seeking a Senior Regulatory Affairs Specialist to be responsible for product registration and all regulatory aspects of post-market surveillance. The Regulatory Affairs Specialist ...

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📑 The Role Answering questions from customers Supporting customer service for tenders Assisting cross-functional teams with product launches Reviewing promotional materials in both French and Dutch Updating regulatory documents and internal databases Keeping track of regulatory changes in Benelux Attending internal meetings w ...

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📑 Regulatory Affairs Specialist – CVRMLocation: LondonCompetitive Salary and BenefitsClosing date: 5th May 2024Introduction to Role:Join our CVRM Regulatory Team as a Regulatory Affairs Specialist and embrace the opportunity to shape the future of healthcare. Be part ...

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📑 Senior Regulatory Specialist - Biocides - Hybrid/Remote Are you a Senior Regulatory Specialist / Regulatory Affairs Manager who would you like to work with a fast-growing business with lots of technical development planned for the next 3 years?? The role of Senior Regulatory Specialist offers you the chance to work with a globa ...

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📑 The Role Answering questions from customers Supporting customer service for tenders Assisting cross-functional teams with product launches Reviewing promotional materials in both French and Dutch Updating regulatory documents and internal ...

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📑 SEE designs and delivers packaging solutions that protect essential goods transported worldwide, preserve food, enable e-commerce and digital connectivity, and help create a global supply chain that is touchless, safer, less wasteful, and more resilient. Our people are entrepreneurial innovators and problem solvers committed to bringing u ...

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📑 Regulatory Affairs Specialist – CVRM Location: London Competitive Salary and Benefits Closing date: 5th May 2024 Introduction to Role: Join our CVRM Regulatory Team as a Regulatory Affairs Specialist and embrace the opportuni ...

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📑 About Us Oxford Nanopore Technologies is headquartered at the Oxford Science Park outside Oxford, UK, with satellite offices and commercial presence in many global locations across the US, APAC and Europe. Oxford Nanopore employs from multiple subject areas including nanopore science, molecular biology and applications, informatics, engineering, el ...

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📑 SEE designs and delivers packaging solutions that protect essential goods transported worldwide, preserve food, enable e-commerce and digital connectivity, and help create a global supply chain that is touchless, safer, less wasteful, and more resilient. Our people are entrepreneurial innovators and problem solvers committed to bringing unique insi ...

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📑 About Us Oxford Nanopore Technologies is headquartered at the Oxford Science Park outside Oxford, UK, with satellite offices and commercial presence in many global locations across the US, APAC and Europe. Oxford Nanopore employs from multiple subject areas including nanopore science, molecular biology and applications, informatics ...

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📑 Regulatory Affairs Specialist – CVRM Location: London Competitive Salary and Benefits Closing date: 5th May 2024 Introduction to Role: Join our CVRM Regulatory Team as a Regulatory Affairs Specialist and embrace the opportunity to shape the future of healthcare. Be part of changing the practice of medicine forever. In this r ...

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📑 Senior Regulatory Specialist - Biocides - Hybrid/Remote Are you a Senior Regulatory Specialist / Regulatory Affairs Manager who would you like to work with a fast-growing business with lots of technical development planned for the next 3 years?? The role of Senior Regulatory Specialist offers you the chance to work with a globally recognised bu ...

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📑 Regulatory Affairs Specialist - London - 12-Month Contract Do you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced C&Q Lead to oversee one of th ...

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📑 TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives. Quality and Regulatory Specialist As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to delive ...

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📑 Regulatory Affairs Associate| Pharmaceutical Industry | UK & Ireland Proclinical are seeking a dedicated professional to manage the operational and technical aspects of regulatory affairs for our UK, Ireland, and Maltese marketing affiliates. Responsibilities: - Execute the Regulatory Plan to ensure the success of new produ ...

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📑 TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives. Quality and Regulatory Specialist As the Quality and Regulatory Specialist, you will play a pivotal role in my cl ...

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📑 Global Regulatory Affairs – Due Diligence Manager / Senior ManagerYour newpany This US Biotech are looking for a Regulatory Affairs professional with strong Due Diligence experience to join an exciting, high-profile project, this is initially a 6 month contract but has scope for extension. There is the option to be fully remote.<br ...

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📑 The Role This is an exciting opportunity for someone develop their career in Regulatory Affairs in a market leading, medical devices company. You’ll be responsible for ensuring their supply chain operations comply with all relevant quality legislation. Creating, updating, and reviewing technical files for ClassI-IIb Medical Devices Post ...

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📑 The Role This is an exciting opportunity for someone develop their career in Regulatory Affairs in a market leading, medical devices company. You’ll be responsible for ensuring their supply chain operations comply with all relevant quality legislation. Creating, updating, and reviewing technical files for ...

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📑 Senior Legal Counsel - Regulatory Law EMEA - 2406180718W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Thr ...

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📑 About the job In the context of our growing activities, we are looking for a Regulatory Affairs Specialist to join our teams in the United Kingdom. You will integrate a team of dedicated Regulatory Affairs professionals and will have the mission to develop PLG’s local UK Regulatory Affairs presence, taking responsibility for new regulatory ...

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📑 Overview Werfen Werfen, founded in , is a worldwide developer, manufacturer and distributor of specialized diagnostic instruments, related reagents, automation workcells, and data management solutions for use primarily in hospitals and independent clinical laboratories. The Company’s business lines include Hemostasis, Acute Care, and Auto ...

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📑 Limbic is making mental healthcare available to everyone, everywhere.Limbic’s vision is to ensure the highest quality therapy is accessible to everyone, everywhere. The way we do that is by deploying AI responsibly, using it to augment clinical care and reduce barriers to accessing therapy at scale. Limbic is already used ...

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📑 Limbic is making mental healthcare available to everyone, everywhere.Limbic’s vision is to ensure the highest quality therapy is accessible to everyone, everywhere. The way we do that is by deploying AI responsibly, using it to augment clinical care and reduce barriers to accessing therapy at scale. Limbic is already used in over 30% of Talking The ...

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📑 Overview Werfen Werfen, founded in , is a worldwide developer, manufacturer and distributor of specialized diagnostic instruments, related reagents, automation workcells, and data management solutions for use primarily in hospitals and independent clinical laboratories. The Company’s business lines inc ...

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📑 About the job In the context of our growing activities, we are looking for a Regulatory Affairs Specialist to join our teams in the United Kingdom. You will integrate a team of dedicated Regulatory Affairs professionals and will have the mission to develop PLG’s local UK Regulatory Affairs presence, taking res ...

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📑 Registration & Regulatory Affairs Specialist • Location: Frimley, UK • Function: GSARA (global safety assessment and regulatory affairs) About the role The Global Registration and Regulatory Compliance (GRRC) team provide regulatory leadership, expertise and execution for the information/dossier develop ...

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📑 Overview Werfen Werfen, founded in , is a worldwide developer, manufacturer and distributor of specialized diagnostic instruments, related reagents, automation workcells, and data management solutions for use primarily in hospitals and independent clinical laboratories. The Company’s business lines in ...

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📑 Registration & Regulatory Affairs Specialist • Location: Frimley, UK • Function: GSARA (global safety assessment and regulatory affairs) About the role The Global Registration and Regulatory Compliance (GRRC) team provide regulatory leadership, expertise and execution for the information/dossier development, product registration and lifecyc ...

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📑 Overview Werfen Werfen, founded in , is a worldwide developer, manufacturer and distributor of specialized diagnostic instruments, related reagents, automation workcells, and data management solutions for use primarily in hospitals and independent clinical laboratories. The Company’s business lines include Hemostasis, Acute Care, and Autoi ...

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📑 Regulatory Affairs Officer (Hybrid working) I currently have a great opportunity for a Regulatory Affairs Officer to progress or start their career within Parallel import. This position is open for both Regulatory and Quality Assurance professionals, so please if you are unsure, give me a call 01925 909045. Key responsibilities for the Regula ...

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📑 An exciting opportunity for an experienced Regulatory Affairs Officer to join a global company in the North West. As a Regulatory Affairs Officer you will be responsible for product compliance following UK and EU REACH guidelines and acting as a mentor to less experienced staff. If you are looking for a step up in your current role then please app ...

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📑 Regulatory Affairs Officer (Hybrid working) I currently have a great opportunity for a Regulatory Affairs Officer to progress or start their career within Parallel import. This position is open for both Regulatory and Quality Assurance professionals, so please if you are unsure, give me a call 01925 909045. Key responsi ...

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📑 An exciting opportunity for an experienced Regulatory Affairs Officer to join a global company in the North West. As a Regulatory Affairs Officer you will be responsible for product compliance following UK and EU REACH guidelines and acting as a mentor to less experienced staff. If you are looking for a step up in your current role then please ...

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📑 Role Overview We are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products within the UK, focusing on CMC, clinical, safety, and product inf ...

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📑 The Role I'm recruiting for a Regulatory Affairs Manager - Biocides to manage a small team whilst remaining hands on, delivery projects to strict timescales and ensuring all professional biocidal products remain compliant with the relevant legislation. You'll be responsible for; End to end regulatory affairs for new and existing professiona ...

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📑 Medical Affairs Director (Remote)Reporting directly to the General Manager, the Medical Affairs Director will play a key part in developing and driving effective Medical Affairs plans for the UK. Our client is a Swiss specialty pharmaceutical company focused on the development and commercialization of innovative medicines for rare neuromuscular dis ...

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📑 Medical Affairs Director (Remote)Reporting directly to the General Manager, the Medical Affairs Director will play a key part in developing and driving effective Medical Affairs plans for the UK. Our client is a Swiss specialty pharmaceutical company focused on the development and commercialization of innovative medicines for rare neuromuscular dis ...

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📑 Medical Affairs Director (Remote)Reporting directly to the General Manager, the Medical Affairs Director will play a key part in developing and driving effective Medical Affairs plans for the UK. Our client is a Swiss specialty pharmaceutical company focused on the development and commercialization of innovative medicines for rare neuromuscular dis ...

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📑 Regulatory Affairs Manager – UK and Ire CosmeticsYour newpany This household name is looking for an experienced Regulatory Affairs Manager / Senior Manager to join their UK and Ire Cosmetics team. This role is mostly remote with 2 days required onsite in Buckinghamshire.Your new role As Regulatory Affairs Manager / ...

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📑 Role Overview Are you looking for a new opportunity where your expertise will be pivotal in navigating the complexities of UK/EU regulatory frameworks? Based in Berkshire, this role offers the chance to become an integral part of a leading Pharmaceutical company, ensuring that innovative health solutions reach the market efficiently and safel ...

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📑 Location: London, Greater London, United Kingdom Type: Contract Job #25229 Are you an experienced Regulatory Affairs professional with a background in Chemistry, Manufacturing and Controls and experience working in the Biopharmaceutical/Biotechnology industry, and are you looking for a new opportunity? We have your next role, we ar ...

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📑 The Role I'm recruiting for a Regulatory Affairs Manager - Biocides to manage a small team whilst remaining hands on, delivery projects to strict timescales and ensuring all professional biocidal products remain compliant with the relevant legislation. You'll be responsible for; End to end regulatory affairs ...

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📑 The Role I'm recruiting for a Regulatory Affairs Manager - Biocides to manage a small team whilst remaining hands on, delivery projects to strict timescales and ensuring all professional biocidal products remain compliant with the relevant legislation. You'll be responsible for; End to end regulatory affairs ...

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📑 Role Overview We are currently looking for a Senior Regulatory Affairs Officer to join a leading Pharmaceutical company based in the Kent area. As the Regulatory Affairs Manager, you will play a pivotal role in managing the life cycle and post-authorisation changes for products within the UK, focusing on CMC, clinical, sa ...

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