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📑 QbD Belgium Regulatory affairs Table of Contents At QbD our RA Services go from regulatory strategy, clinical, CTD registration dossier writing, eCTD compilation and submission to competent authorities to Vigilance. We support from idea to commercialization. Do you want to ensu ...

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📑 Senior or Principal Scientist Dissolution Sciences - 2306155317W **Description** **Based on your professional experience and educational background, we have the flexibility to tailor the position's level and responsibilities accordingly.** Dissolution Sciences is part of the Global Analytical Development organization with ...

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📑 QbD Belgium Regulatory affairs Table of Contents At QbD our RA Services go from regulatory strategy, clinical, technical file to Vigilance. We support from idea to commercialization. Do you want to support companies throughout the entire medical device regulatory lifecycle? Do ...

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📑 As a leading global animal health company, Elanco delivers innovative products and services to improve the health of pets and farm animals around the world because we believe making animals' lives better, makes life better. Since 1954, we have provided solutions that support veterinarians, farmers and pet owners to advance our vision of Food ...

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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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📑 RA Belgium Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations. Our objective is to provide ma ...

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📑 QbD Belgium, The Netherlands Clinical, Regulatory affairs Table of Contents Do you have a passion for technical, scientific writing? Do the words “responsible, communicative & effective” fit you perfectly? Then don’t hesitate and apply for this position! What do ...

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📑 Qarad Belgium Clinical, Regulatory affairs Table of Contents Are you excited about science and technology? Do you love to dig into scientific data to investigate the performance of that new diagnostic test? Do you enjoy coordinating and making sure the job gets done according t ...

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📑 Qarad Belgium, The Netherlands Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations. Our object ...

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📑 Associate Director in Solid State Sciences & Characterization - 2406176813W **Description** Pharmaceutical & Material Sciences is, within the Pharmaceutical Development & Supply (PPDS) organization of the Pharmaceutical Companies of Johnson and Johnson, responsible for preformulation & biopharmaceutics, solid state form selection ...

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📑 QbD, Sales The UK Table of Contents The UK team of the international QbD group is a specialist regulatory and pharmacovigilance consultancy company . Our services consist in providing consultation throughout product development, regulatory approval, market launch, and into ...

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📑 Position SGS is currently looking for a Final Reviewer/Certification Decision Maker for the SGS Notified Body in Antwerp. The main responsibilities will be to provide third party certification review and decision prior to certificate issue in line with SGS policies and procedures and ...

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📑 QbD clinical Belgium Clinical Table of Contents WHAT ARE YOUR MAIN RESPONSIBILITIES? The Medical Writer is responsible for authoring, reviewing and editing clinical trial-related documents (including regulatory documents) and scientific publications. ...

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📑 QbD HQ, Sales Belgium, The Netherlands, The UK Table of Contents The QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for ...

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📑 Job Description As a Product Assessor , you will play a crucial role in our organization by overseeing Sterilization product assessments and conducting technical file reviews in strict adherence to regulatory requirements, including the European Medical Device Directive and Medical Device Regul ...

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📑 Our client is a leading mid-sized, family-like company in Belgium, operating across different production sites. With a diverse portfolio spanning cosmetics, food supplements, and pharmaceutical products, our client offers a unique opportunity for professionals seeking a dynamic and interesting career. Working closely with different peop ...

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📑 Qarad Belgium Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations. Our objective is to provide ...

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📑 Qarad Belgium Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations. Our objective is to provide ...

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📑 Our client is a leading mid-sized, family-like company in Belgium, operating across different production sites. With a diverse portfolio spanning cosmetics, food supplements, and pharmaceutical products, our client offers a unique opportunity for professionals seeking a dynamic and interesting career. Working closely with different peop ...

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📑 Scientist MSAT Emerging Technology - 2406183520W **Description** Janssen Pharmaceutica NV, a part of the Johnson & Johnson Family of Companies is recruiting for a Scientist, MSAT Emerging Technologies, located in Beerse, Belgium. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation ...

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📑 RA Belgium Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations . Our objective is to p ...

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📑 **JOIN US ON OUR EXCITING JOURNEY!** IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, tech ...

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📑 Material Scientist - 2406173985W **Description** **About Johnson & Johnson** 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 ...

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📑 At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call ‘connectors', people ...

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📑 Clinical Belgium Clinical, Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations . Our o ...

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📑 Software Belgium Software validation Table of Contents Do you have in addition to your passion for regulatory affairs, also an affinity with IT? Would you like to be a part of QbD’s Software & Services Division and specialize in Medical Device Software Validation? Then apply no ...

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📑 From values to valueAckermans & van Haaren’s (AvH) mission is “to be your partner for sustainable growth”. For almost 150 years, we have invested alongside partners with whom we share the same long-term vision and values, creating sustainable growth. That’s what sets us apart. We believe that putting sustainability front and ...

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📑 QbD Belgium, The Netherlands Quality management Table of Contents Do you have the skills and motivation to take full responsibility for the product release at our clients in the pharmaceutical industry? Apply now! What do we expect from you as a Qualified Perso ...

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📑 Associate Regulatory Site Officer Antwerpen 4-6 jaar en 6-9 jaarBachelor en Master / PHDFarma Geplaatst op 15-04- Over de functie Als Associate Regulatory Site Officer zal je ondersteuning bieden bij de regulatory CMC-dossierbeheersactiviteiten voor verschillende farmaceutische product ...

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📑 QbD clinical Belgium Clinical Table of Contents Do you want to make an impact as Clinical Research Professional? Do you want to protect the safety & well-being of subjects and guarantee data quality? Do you get energy from daily communication with investigators, study coordinat ...

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📑 QA Table of Contents Quality Assurance (QA) consultant ATMP Are you eager and enthusiastic to improve quality within the cell and gene therapy sector? We are looking for a new colleague with thorough knowledge on QA proce ...

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📑 ASSET MANAGEMENT - COMPLIANCE - AML - REGULATORY - UHNWI - ANTWERPStay vigilant on regulatory shifts, evaluating their repercussions on current business methodologies.Direct the execution of projects, initiatives, procedures, and measures in response to the fluid legal and sectoral environment.Execu ...

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📑 QbD Belgium, The Netherlands Clinical, Qualification & Validation, Quality management, Regulatory affairs, Software validation Are you an expert within medical devices and passionate by helping companies in this area in their growth or to achieve their ISO13485 certificate? Apply now for the job of medical dev ...

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📑 Client Manager (CM) - Genomics Are you looking to make your next career move? CellCarta, a Contract Research Organization, is hiring a Client Manager (CM) - Genomics to join our dynamic team. As a CM - Genomics you will have the opportunity to use your expertise and skills to ensure that our services meet the highest industry standards. Come work w ...

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📑 RA Austria Regulatory affairs Table of Contents QbD Austria , part of the international QbD group, is a young and growing consulting company offering services and training on regulatory affairs, regulatory compliance, business organization and quality assurance ...

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📑 RA The UK Regulatory affairs Table of Contents The UK team of the international QbD group, is a specialist regulatory and pharmacovigilance consultancy company. Our services consist in providing consultation throughout product development, regulatory approval, ...

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📑 RA Austria Regulatory affairs Table of Contents QbD Austria , part of the international QbD group, is a young and growing consulting company offering services and training on regulatory affairs, regulatory compliance, business organization and quality assurance ...

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📑 RA Austria Regulatory affairs Table of Contents QbD Austria , part of the international QbD group, is a young and growing consulting company offering services and training on regulatory affairs, regulatory compliance, business organization and quality assurance ...

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📑 Clinical Belgium Table of Contents Do you want to make an impact as Senior Operations Lead, Clinical Division? Do you get energy from daily communication with study teams and clients? Do the cornerstones of Operations within Clinical Development have no more secrets for you? Then you might ...

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📑 Scientist, Regulatory CMC Dossier – Biotherapeutics - 2406181251W **Description** Janssen Research & Development, L.L.C., a division of Johnson & Johnson's Family of Companies, is recruiting for a Scientist, Regulatory CMC Dossier - Biotherapeutics based in Spring House, PA. Remote work options may be considered on a case-by-case ...

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📑 QbD clinical Belgium Table of Contents The QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in ATMP, ...

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📑 QbD The UK Quality management, Regulatory affairs Table of Contents The UK team of the international QbD group, is a specialist regulatory and pharmacovigilance consultancy company. Our services consist in providing consultation throughout product development, ...

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📑 DescriptionResponsibilities:Utilize comprehensive knowledge of regulations to advise and support business units on compliance matters.Provide guidance and consultation on code of conduct, regulatory compliance, and related policies.Collaborate with internal stakeholders ...

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📑 ERM is looking for a motivated, detail-oriented entry level Environmental Engineer or Scientist to join the Liability Portfolio Management and Remediation (LPMR) team as a Junior Consultant in Brussels or Antwerp. Working under the direction of project managers, team leaders and partners, the successful candidate will work on i ...

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📑 Mazars is an internationally integrated partnership, specialising in audit, accountancy, advisory, tax and legal services. Operating in over 90 countries and territories around the world, we draw on the expertise of more than 42,000 professionals to assist clients of all size ...

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📑 Associate Director, Temperature Strategy & Execution - 2406177829W **Description** Johnson & Johnson Innovative Medicine Research & Development (JJIM R&D), part of the Johnson & Johnson Family of Companies, is recruiting for an Associate Director, Temperature Strategy & Execution within Clinical Supply Chain (CSC). The position ca ...

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📑 Clinical Project Manager Are you looking for an exciting new career opportunity? CellCarta, a renowned Contract Research Organization, is actively seeking a highly skilled and motivated Clinical Project Manager to join our dynamic team. As a Project Manager, you will have the opportunity to use your expertise and skills to ensure that our services ...

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📑 Oliver James is looking a Junior consultant who want to work in the world of finance in Belgium.You will play a crucial role in ensuring compliance with regulatory requirements and mitigating financial and reputational risks associated with onboarding new customers. You will conduct thorough investigations into ...

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📑 Mgr Supply Chain Transfer Mgmt - 2406182808W **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. Through our exp ...

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📑 Job DescriptionAs Senior Manager Actuarial Sciences, the candidate will report to the Associate Partner and will be responsible for the following tasks:Consulting missionsThe candidate will personally perform and lead consulting missions or projects at our customers, thereby using his/her personal experti ...

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