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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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📑 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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📑 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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📑 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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📑 Senior Medical Writer - Global Med Comms Agency - Remote, UKPhenomenally excited to be partnering with my Global Med Comms Agency client to support them in their search for a Senior Medical Writer to join thriving their UK team.We are looking for a Senior Medical Writer, ideally from a Med Comms background, who has been exposed to working on Public ...

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📑 Senior Medical Writer - Global Med Comms Agency - Remote, UKPhenomenally excited to be partnering with my Global Med Comms Agency client to support them in their search for a Senior Medical Writer to join thriving their UK team.We are looking for a Senior Medical Writer, ideally from a Med Comms background, who has been exposed to working on Public ...

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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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📑 BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: ...

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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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📑 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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📑 Job Title: Medical Information Specialist - German SpeakingLocation: Remote (based in UK)Salary: CompetitiveJob DescriptionPlanet Pharma are currently partnered with a leading global Research Consulting Organization providing services to the Pharmaceutical, Medical Device and Biotechnology industries across the world. Our client is currently seekin ...

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📑 Job Title: Medical Information Specialist - German SpeakingLocation: Remote (based in UK)Salary: CompetitiveJob DescriptionPlanet Pharma are currently partnered with a leading global Research Consulting Organization providing services to the Pharmaceutical, Medical Device and Biotechnology industries across the world. Our client is currently seekin ...

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📑 Description FSP Senior Clinical Research Associate II Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the custome ...

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📑 As a Senior Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. As a Senior Medical Writer you will be supporting a Top-5 pharma company. You have the chance to help our customer to deliver best-in-class regulatory and submission documents. While ...

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📑 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma ...

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📑 **Job Description** 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 g ...

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📑 Job Title: Senior Regulatory Affairs AssociateLocation: 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 Overview:As a Seni ...

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📑 Job Title: Senior Regulatory Affairs AssociateLocation: 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 Overview:As a Seni ...

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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 - Food Manufacturing BusinessCompany: True North Talent RecruitmentLocation: Fully Remote/ Home BasedPosition: Regulatory Affairs Advisor – Fluent in ArabicSalary: 28-38k full benefits package see belowAbout Us: True North Talent is a recruitment company, dedicated to connecting exc ...

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📑 Title: Clinical Trial Manager - Global Pharma - Complex TrialsLocation: LondonDuration: Full TimeSalary: Competitive Based on ExperienceWe’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. You will be apart of significant growth within its pipelin ...

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📑 Title: Clinical Trial Manager - Global Pharma - Complex TrialsLocation: LondonDuration: Full TimeSalary: Competitive Based on ExperienceWe’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. You will be apart of significant growth within its pipelin ...

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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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📑 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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📑 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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📑 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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📑 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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📑 What if the work you did every day could impact the lives of people you know? Or all of humanity?At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of dis ...

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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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📑 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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📑 When our values align, there's no limit to what we can achieve. We are currently seeking Regulatory Affairs Professionals with experience in Clinical Trial Applications (CTAs) under the EU-CTR directive. Join our team or work on dedicated client projects as a Senior Regulatory Affairs Consultant, Regulatory Affairs Consultant or Regulatory ...

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📑 Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and ...

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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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📑 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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📑 Role Summary With an expanding regulatory team, an exciting opportunity has arisen for a Director to join the Autolus Regulatory and Medical Writing team to support global expansion of our cell and gene therapy products. This position requires a medical writing professional with a proven track record of successfully w ...

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📑 Regulatory Affairs and Quality Assurance Assistant - Medical Devices - Cambridge Due to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with and support the company's Quality Assurance and Regulatory Affairs Manager. The team provide quality assurance and ...

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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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📑 About the Role :   We are building our documentation team and are looking for a Technical Writer to help lead the end-to-end vision, strategy, and implementation of Redpanda products. Reporting to the Technical Writing Manager, you will document multiple functional areas of Redpanda ...

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📑 Principal Medical Writer (EMEA) (FSP; Remote) At Thermo Fisher Scientific, you will 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 resour ...

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📑 When our values align, there's no limit to what we can achieve. We are currently seeking Regulatory Affairs Professionals with experience in Clinical Trial Applications (CTAs) under the EU-CTR directive. Join our team or work on dedicated client projects as a Senior Regulatory Affairs Consultant, Regulator ...

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📑 *This is a permanent position based in Dubai. Relocation assistant is provided. About The Opportunity:We are seeking a highly skilled and analytical Crypto Research Writer/Analyst to join our team! The ideal candidate will have a strong background in finance and data analysis, coupled with in-depth knowledge of the cryptocurrency industry. This rol ...

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📑 Regulatory Affairs and Quality Assurance Assistant - Medical Devices - Cambridge Due to the growth of a medical devices company based in Cambridge, there is need for a new Regulatory Affairs and Quality Assurance Assistant to work with and support the company's Quality Assurance and Regulatory Affairs Manager. The team provide qual ...

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📑 Working directly with the portfolio managers, the Investment Writer will take responsibility for the following duties: Working side by side with the portfolio management team and analysts to obtain technical knowledge that informs content production. Crafting engaging and sophisticated commentaries that discuss economic market outlooks for investo ...

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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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📑 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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