📑 Precision for Medicine (CRO) are recruiting a Regulatory Manager to join our team, candidates can be based in the following countries: UK, Spain, Hungary, Slovakia, Serbia, Romania or Poland.The Regulatory Manager (RM) provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, ...
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📑 Ref: 37326Legal Counsel (Regulatory) Location: LondonSalary: Competitive + Bonus + BenefitsReports to: Senior Legal CounselRole type: Permanent/ Full TimeWFH: < ...
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📑 Regulatory Lawyer Job Opportunity in Manchester - areas: HSE Regulatory; Compliance; Environmental; and Health and Safety Regulatory Solicitor Manchester – will also consider Legal Executives and Paralegals This is an exciting opportunity with a rapidly growing regulatory team operating across the UK. They are looking to attract solicitors with a r ...
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📑 Regulatory Lawyer Job Opportunity in Manchester - areas: HSE Regulatory; Compliance; Environmental; and Health and Safety Regulatory Solicitor Manchester – will also consider Legal Executives and Paralegals This is an exciting opportunity with a rapidly growing regulatory team operating across the UK. They are looking to attract solicitors with a r ...
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📑 Job summaryWe are currently looking for a number of Regulatory Engagement Managers to join us at the Regulator of Social Housing.� Join us in promoting a viable, efficient and well-governed social housing sector, ensuring the delivery and maintenance of suitable, quality housing.Job descriptionAs the Regula ...
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📑 ABOUT US We are a trusted partner in protecting brands and their end-consumers around the world, through clear and accurate product information. Creating trust: Consumers must be able to trust product information, in order to trust a brand. When our clients choose to work with us, they are trusting ...
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📑 Murray McIntosh are delighted to be partnering with Rockwool who are looking for a regulatory affairs specialist to join their accomplished team. Actively engaged in discussions to drive quality and sustainability in the built environment, Rockwool are a premium brand in manufacturing insulation products designed to meet the challenges ...
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📑 Regulatory Affairs Custom Device Team Lead / Senior Regulatory Affairs Custom Device AssociateMain Purpose of Job and Objectives:Perform Regulatory tasks to ensure compliance with regulations.Prepare regulatory documentation and submissions for product approvals.Develop regulatory plans/strategies for new products and changes to existing products.P ...
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📑 Job Title: Regulatory Affairs – Senior CMC Dossier ManagerJob Type: Contract position until December 2024, inside IR35Rate: Up to £85ph PAYE or UmbrellaLocation: UK or Europe (Remote-based)CPL has partnered with a world-leading Biotech looking for an experienced Regulatory CMC leader to work on a developing rare disease portfolio. This will be supp ...
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📑 Job Title: Regulatory Affairs – Senior CMC Dossier ManagerJob Type: Contract position until December 2024, inside IR35Rate: Up to £85ph PAYE or UmbrellaLocation: UK or Europe (Remote-based)CPL has partnered with a world-leading Biotech looking for an experienced Regulatory CMC leader to work on a developing rare disease portfolio. This will be supp ...
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📑 Christeyns is a privately owned detergents and chemicals group, with activities in several markets worldwide, completely focused on a B-2-B environment. Our head office is located in Ghent, Belgium. The Group employs about people across 30 countries. Over the last 15 years, Christeyns has enjoyed rapid growth of around 15% per year and now has ...
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📑 Austin Vita are pleased to offer an exciting opportunity for a hands on Regulatory Engineer to join our client, an innovative medical device business who design, develop and manufacture a range of devices for global markets based in Buckinghamshire. This will be a site based role so suit someone who loves working in a Team and rolling up their slee ...
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📑 Regulatory Affairs Custom Device Team Lead / Senior Regulatory Affairs Custom Device AssociateMain Purpose of Job and Objectives:Perform Regulatory tasks to ensure compliance with regulations.Prepare regulatory documentation and submissions for product approvals.Develop regulatory plans/strategies for new products and changes to existing products.P ...
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📑 Overview At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many ...
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📑 Company DescriptionSGS provide the worlds most comprehensive range of integrated inspection, testing, certification, and advisory services, powered by the latest technology and digital tools. Our global network of experts supports our customers by helping them to meet increasingly complex regulations and standards.At SGS, we believe in rewarding ou ...
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📑 Company DescriptionSGS provide the worlds most comprehensive range of integrated inspection, testing, certification, and advisory services, powered by the latest technology and digital tools. Our global network of experts supports our customers by helping them to meet increasingly complex regulations and standards.At SGS, we believe in rewarding ou ...
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📑 Regulatory Affairs Specialist - Lifecycle MaintenanceLocation: RemoteWe are seeking an experienced Regulatory Affairs Specialist to oversee lifecycle maintenance for our mature product portfolio. The successful candidate will manage compliance activities, coordinate with EU member states under the MRP, handle national product regulations, and ensur ...
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📑 I am working with a growing pharmaceutical company who provide over-the-counter (OTC) pharmaceutical products dedicated to enhancing the health and well-being of customers. They're currently in the next phase of growth for the company as they're overtaking a consumer portfolio from a huge company in the pharmaceutical industry.....Position Overview ...
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📑 I am working with a growing pharmaceutical company who provide over-the-counter (OTC) pharmaceutical products dedicated to enhancing the health and well-being of customers. They're currently in the next phase of growth for the company as they're overtaking a consumer portfolio from a huge company in the pharmaceutical industry.....Position Overview ...
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📑 Regulatory Affairs Specialist - Lifecycle MaintenanceLocation: RemoteWe are seeking an experienced Regulatory Affairs Specialist to oversee lifecycle maintenance for our mature product portfolio. The successful candidate will manage compliance activities, coordinate with EU member states under the MRP, handle national product regulations, and ensur ...
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📑 Our client, a successful and growing Biotechnology organisation, is looking to hire a new addition to the Regulatory CMC team.This role is responsible for preparing regulatory CMC submission strategy for rare disease drugs (both biologics and small molecules) and an opportunity to design creative solutions in order to obtain approval for initial BL ...
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📑 Our client, a successful and growing Biotechnology organisation, is looking to hire a new addition to the Regulatory CMC team.This role is responsible for preparing regulatory CMC submission strategy for rare disease drugs (both biologics and small molecules) and an opportunity to design creative solutions in order to obtain approval for initial BL ...
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📑 Role Summary An exciting opportunity has arisen for an experienced CMC Regulatory Affairs Sr. Director to join the Autolus team to take a leadership role for developing global CMC regulatory strategies and content plans for products across Autolus’ cell and gene therapy portfolio. Autolus is looking for a CMC Regulatory Affairs Sr. Dire ...
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📑 Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remoteCompany Description:We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies.Our commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team.Position Overvie ...
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📑 Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remoteCompany Description:We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies.Our commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team.Position Overvie ...
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📑 Overview At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many ...
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📑 Rev & Regs are recruiting for a Head of Risk & Compliance role for a rapidly growing tech-focussed Capital Markets company.Reporting to the Chief Operating Officer, the Head of Risk & Compliance will work closely with the board to develop fit for purpose Compliance Frameworks, Policies & Procedures, and implement and embed the companywide Risk Mana ...
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📑 Rev & Regs are recruiting for a Head of Risk & Compliance role for a rapidly growing tech-focussed Capital Markets company.Reporting to the Chief Operating Officer, the Head of Risk & Compliance will work closely with the board to develop fit for purpose Compliance Frameworks, Policies & Procedures, and implement and embed the companywide Risk Mana ...
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📑 tranScrip is a leading drug development partner who, in the last 2 decades, has supported over 500 clients deliver many development programmes and regulatory submissions.tranScrip has an excellent reputation for providing strategic regulatory support and for delivering regulatory documents and processes. Our team is growing, and we are searching fo ...
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📑 The RoleThis is a superb opportunity to join an established law firm that offers specialist quality legal advice to both businesses and individuals.The firm is recognised for its outstanding client care and high-quality Crime and Regulatory work, among other highly regarded practice areas.Due to the development and expansion of the firm, they are n ...
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📑 Regulatory Affairs Advisor (French Speaking)At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised for our expertise in the interpretation and commercial ...
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📑 tranScrip is a leading drug development partner who, in the last 2 decades, has supported over 500 clients deliver many development programmes and regulatory submissions.tranScrip has an excellent reputation for providing strategic regulatory support and for delivering regulatory documents and processes. Our team is growing, and we are searching fo ...
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📑 The RoleThis is a superb opportunity to join an established law firm that offers specialist quality legal advice to both businesses and individuals.The firm is recognised for its outstanding client care and high-quality Crime and Regulatory work, among other highly regarded practice areas.Due to the development and expansion of the firm, they are n ...
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