📑 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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📑 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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📑 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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📑 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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📑 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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📑 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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📑 PE Global is currently recruiting for a Regulatory Affairs CMC Manager for a contract role with a leading multinational Biotech client based in London – Fully remote within the UK.Regulatory CMC support for post-approval submissions for commercial products, predominantly biotechnology products and new international MAA filings predominantly in EMEA ...
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📑 PE Global is currently recruiting for a Regulatory Affairs CMC Manager for a contract role with a leading multinational Biotech client based in London – Fully remote within the UK.Regulatory CMC support for post-approval submissions for commercial products, predominantly biotechnology products and new international MAA filings predominantly in EMEA ...
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📑 We are currently seeking a talented and experienced Regulatory Affairs Project Manager to join our client's team in Surrey. Our client is an established cosmetics/pharmaceuticals company looking for someone with expertise in global cosmetic regulations. In collaboration with a highly skilled international team you will support in the pr ...
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📑 This is an excellent opportunity to join a leading insurance company as a Regulatory Affairs Manager. The successful candidate will be responsible for providing guidance, aid and advice to the company's UK businesses and compliance colleagues on technical compliance matters and regulatory developments. Key Responsibilities: ...
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📑 This is an excellent opportunity to join a leading insurance company as a Regulatory Affairs Manager. The successful candidate will be responsible for providing guidance, aid and advice to the company's UK businesses and compliance colleagues on technical compliance matters and regulatory developments. Key Responsibilities: ...
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📑 By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowle ...
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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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📑 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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📑 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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📑 We are currently seeking a talented and experienced Senior Regulatory Affairs Manager to join our client's team in Surrey. Our client is an established cosmetics/pharmaceuticals company looking for someone with expertise in global cosmetic regulations. In collaboration with a highly skilled international team you will help to manage the ...
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📑 Insulet started in 2000 with an idea and a mission to enable our customers to enjoy simplicity, freedom and healthier lives through the use of our Omnipod® product platform. In the last two decades we have improved the lives of hundreds of thousands of patients by using innovative technology that is wearable, waterproof, and lifestyle accommodat ...
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📑 JOB TITLE : Senior Regulatory Affairs Specialist LOCATION : Remote/Hybrid WORKING HOURS : 37.5 Hours, Monday to Friday A brighter future awaits you At CooperVision, we are proud to be the global leader in contact lenses. At our innovative sites worldwide, we manufacture and distri ...
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📑 Head of Regulatory AffairsAre you looking for a role to lead global regulatory filing strategy?Do you have recent experience of regulatory strategy for novel oncology modalities?Have you worked on programs from preclinical stage to filing and launch?Fraser Dove International is partnering exclusively with an innovative biotechnology organisation sp ...
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📑 Head of Regulatory AffairsAre you looking for a role to lead global regulatory filing strategy?Do you have recent experience of regulatory strategy for novel oncology modalities?Have you worked on programs from preclinical stage to filing and launch?Fraser Dove International is partnering exclusively with an innovative biotechnology organisation sp ...
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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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📑 If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that read over 10 m ...
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📑 Regulatory Affairs Manager – Leading Pharma Specialist Medicines – Manchester (hybrid working) - £competitive salary, 10% bonus, pension + other benefits.Please note: This role is a 12month FTC to cover maternity leave. You'll be a permanent member of staff, with a salary/company benefits, for the 12 months. This is not an hourly/daily rate contrac ...
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📑 Regulatory Affairs Manager – Leading Pharma Specialist Medicines – Manchester (hybrid working) - £competitive salary, 10% bonus, pension + other benefits.Please note: This role is a 12month FTC to cover maternity leave. You'll be a permanent member of staff, with a salary/company benefits, for the 12 months. This is not an hourly/daily rate contrac ...
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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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📑 One of our top 10 pharmaceutical clients are seeking statisticians of various seniority to join and support the companies Statistical research. these roles are working directly in the company and is home based in the UK.The roles are at varying levels detailed below(Associate Manager / Manager) :Exposure to R, SAS, or PythonUnderstanding of regulat ...
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📑 One of our top 10 pharmaceutical clients are seeking statisticians of various seniority to join and support the companies Statistical research. these roles are working directly in the company and is home based in the UK.The roles are at varying levels detailed below(Associate Manager / Manager) :Exposure to R, SAS, or PythonUnderstanding of regulat ...
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📑 At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a s ...
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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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📑 Job title: Associate Director, Regulatory Affairs A Pharmaceutical business in London is looking for an Associate Director, Regulatory Affairs to join their Global team. In this role you will provide strategic regulatory and scientific assessment on preclinical requirements, and clinical development plans to bring new products to patients in the mo ...
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📑 Job title: Associate Director, Regulatory Affairs A Pharmaceutical business in London is looking for an Associate Director, Regulatory Affairs to join their Global team. In this role you will provide strategic regulatory and scientific assessment on preclinical requirements, and clinical development plans to bring new products to patients in the mo ...
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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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📑 Job Title: Pharmaceutical Packaging Artwork Manager Salary: £50-60k basic + bonus + benefits Location: Scotland Reference: J3000 Contact: Telephone: 0141 647 6688 Categories: , , Want to move to one of the most picturesque parts of Scotland, yet with easy access to Edinburgh ...
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📑 Compliance Manager - Global Organisation - Kings Lynn Office - £30k-£40k (DoE) - Part Time ConsideredA global company with offices in Kings Lynn, who is a trailblazer in their field of expertise, is looking for a, detail-minded and accurate Compliance Manager to join their team. The Compliance Manager will provide effectively communicate with clie ...
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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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📑 Compliance Manager - Global Organisation - Kings Lynn Office - £30k-£40k(DoE)- Part Time ConsiderednA global company with offices in Kings Lynn, who is a trailblazer in their field of expertise, is looking for a, detail-minded and accurateCompliance Managerto join their team.nTheCompliance Managerwill provide effectively communicate with clients, s ...
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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 Advisor – French Speaking£33,000 - £39,000HomebasedFood ManufacturingJob ref: 8627The companyThe business provides scientific, technical, and legislative support to the food and beverage industries worldwide. The practical application of technical excellence lies at the heart of all they do and ...
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📑 Role Summary With a significantly expanding regulatory team, an exciting opportunity has arisen for an experienced Global Regulatory Affairs Lead (Senior Director/Executive Director) for AutoImmune to join the Autolus team to expand their cell and gene therapy products. Autolus is looking for a ...
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📑 As an Associate Solicitor, you will help our General Counsel and the Head of Regulatory Affairs to minimize legal and regulatory risk and align with essential business objectives.Responsibilities of the roleSupport our legal and compliance teams, specifically the General Counsel and Head of Regulatory Aff ...
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