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📑 ​RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function. ✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member state ...

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📑 Job Title: Regulatory Affairs Consultant (Cosmetics)Company Overview: A leading company we represent is pharmaceutical company specializing in cosmetics, committed to delivering high-quality and innovative products that enhance the beauty and well-being of our customers. We are seeking a talented Regulatory Affairs Consultant with expertise ...

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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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📑 RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function.✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member states within the past ...

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📑 RBW Consulting are working in partnership with a global mid-sized CRO in their search for a Freelance IVD Regulatory Affairs Consultant based in the EU to start as soon as possible within their IVD function.✔ Local ethics committee submissions and Annex XIV submissions for clinical trial assay across the majority of EU member states within the past ...

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📑 Associate Director (Regulatory Affairs)My client are a dynamic and innovative medical technology company focused on developing advanced healthcare solutions. As we navigate through the transition to the Medical Device Regulation (MDR), we are seeking a highly skilled and experienced professional to join our team as Associate Director of Regulatory ...

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📑 Associate Director (Regulatory Affairs)My client are a dynamic and innovative medical technology company focused on developing advanced healthcare solutions. As we navigate through the transition to the Medical Device Regulation (MDR), we are seeking a highly skilled and experienced professional to join our team as Associate Director of Regulatory ...

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📑 Join the regulatory affairs team at a global pest control products company. Friendly and experienced team Work on compliance and registrations for a global portfolio of products. Duties will be varied and will include biocide product registrations / notifications, gathering data, compiling dossiers, liaison with testing teams, SDS authoring, classi ...

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📑 Join the regulatory affairs team at a global pest control products company. Friendly and experienced team Work on compliance and registrations for a global portfolio of products. Duties will be varied and will include biocide product registrations / notifications, gathering data, compiling dossiers, liaison with testing teams, SDS authoring, classi ...

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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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📑 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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📑 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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📑 Regulatory Affairs Manager - UK and Ire CosmeticsYour new company 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 / Senior Manager in Cosmetics O ...

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📑 Global household name speciality chemical companyResponsibility for National and Regional regulatory compliance Diverse business units – complex aqueous mixtures and substancesBecome a regulatory subject matter expert This will be a highly diverse role; typical duties include answering complex customer regulatory enquiries, researching/impact asses ...

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📑 Global household name speciality chemical companyResponsibility for National and Regional regulatory compliance Diverse business units – complex aqueous mixtures and substancesBecome a regulatory subject matter expert This will be a highly diverse role; typical duties include answering complex customer regulatory enquiries, researching/impact asses ...

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📑 [] Regulatory Affairs Associate (f/m/d) Full or Part Time United Kingdom Young Professional August 01, 2023 Hybrid Remote We are looking for Regulatory Affairs Associate (f/m/d) Tell a friend Apply now All jobs knoell is one of the leading global service providers in offering regulatory r ...

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📑 We're looking for a Senior Regulatory Affairs Specialist to join our innovative client during an exciting development programme. You'll lead in regulatory affairs, focusing on manufacturing regulations and environmental legislation. You'll need an, science, legal, engineering or environmental degree, superb communication skills, ...

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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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📑 BaxMed – Ad-Hoc Senior Regulatory Affairs ConsultantLed by Stuart Baxter, a seasoned professional with a distinguished career in Regulatory Affairs, BaxMed Regulatory Ltd is an exciting early-stage organisation formed to provide Regulatory and Quality Compliance Services for the global Medical Device / healthcare sector. With a core ethos and commi ...

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📑 Senior Consultant – Public and Corporate Affairs – Research/Strategy ConsultancyLondon (Hybrid)£40 – 44,000 + BensOur client is an established and well-regarded research/strategy consultancy with continued growth and a really great range of public and private sector clients. They seek to add a further senior consultant (SRE/RM level) to join their ...

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📑 Senior Consultant – Public and Corporate Affairs – Research/Strategy ConsultancyLondon (Hybrid)£40 – 44,000 + BensOur client is an established and well-regarded research/strategy consultancy with continued growth and a really great range of public and private sector clients. They seek to add a further senior consultant (SRE/RM level) to join their ...

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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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📑 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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📑 Description : Hydrafacial is hiring a Manager, Regulatory Affairs , who is a key contributor in bringing the company’s products into new markets and spearheading global medical device/cosmetic regulatory submissions. Serves as the internal subject matter expert for international regulatory affairs on assigned pr ...

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📑 OUR COMPANY We, at RegASK are a high growth global RegTech company leveraging technology and global network of experts to revolutionize regulatory intelligence, serving the LifeSciences (MedTech, CROs, Pharma) and FMCG industries (Food, Personal Care). RegASK team is highly diverse with more than 10 nationalities across 3 continents, entrepren ...

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📑 *OPPORTUNITY TO RELOCATE TO DUBAI, EARN TAX FREE BASE AND COMMISSION SALARYLife Science Recruitment Consultant / US & Global Market Office based in the Marina area of DubaI, UAEOpportunity for an experienced 360 life science market recruiter to join a Dubai based business at Associate / Recruitment Consultant / Senior Recruitment Consultant level. ...

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📑 *OPPORTUNITY TO RELOCATE TO DUBAI, EARN TAX FREE BASE AND COMMISSION SALARYLife Science Recruitment Consultant / US & Global Market Office based in the Marina area of DubaI, UAEOpportunity for an experienced 360 life science market recruiter to join a Dubai based business at Associate / Recruitment Consultant / Senior Recruitment Consultant level. ...

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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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📑 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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📑 Regulatory Affairs Consultant CMC, biologics outside of IR35Your new companyThis growing US rare disease company is looking for an experienced Regulatory Affairs CMC (biologics) professional to join them on a 12-month contract, this contract job is outside of IR35 and can be fully remote or hybrid working.Your new roleAs Regulatory Affairs Consulta ...

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📑 Are you an experienced regulatory affairs writer looking for a new challenge? We have just the opportunity for you! Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role offers a stimulating work environment at the forefront of medical research, along with ample opportunit ...

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📑 Are you an experienced regulatory affairs writer looking for a new challenge? We have just the opportunity for you! Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role offers a stimulating work environment at the forefront of medical research, along with ample opportunit ...

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📑 Are you an experienced regulatory affairs writer looking for a new challenge? We have just the opportunity for you! Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role offers a stimulating work environment at the forefront of medical research, along with ample opportunit ...

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📑 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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📑 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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📑 Exciting Opportunity for Regulatory Affairs AVP:Are you a regulatory compliance expert seeking your next career move? My client are a Global banking organisation on the lookout for a talented individual to join our team as a Regulatory Affairs Assistant Vice President (AVP).Key Responsibilities:Develop and maintain relationships with UK regulators, ...

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📑 Exciting Opportunity for Regulatory Affairs AVP:Are you a regulatory compliance expert seeking your next career move? My client are a Global banking organisation on the lookout for a talented individual to join our team as a Regulatory Affairs Assistant Vice President (AVP).Key Responsibilities:Develop and maintain relationships with UK regulators, ...

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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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📑 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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📑 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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📑 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 Consultant CMC, biologics outside of IR35Your newpany This growing US rare diseasepany is looking for an experienced Regulatory Affairs CMC (biologics) professional to join them on a 12-month contract, this contract job is outside of IR35 and can be fully remote or hybrid working.Your new role As ...

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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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📑 1,800+ associates. 86 countries. One Regulatory Affairs. At Novartis your voice, experience, and quality mindset can truly make a difference in Regulatory Affairs (RA). Novartis has a unique and promising portfolio with 70 projects as potential NMEs in development, 65 projects in Phase 3 or already undergoing registration, and 100 Phase 1/2 project ...

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📑 Our client is a clinical-stage R&D company that is developing an innovative treatment for solid tumour oncology. We are looking for an experienced medical device Regulatory Affairs and Quality Assurance (QA) professional to join the team in this executive role. The role manages the QA Director and reports to the CEO of the company. ...

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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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