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📑 Head of Regulatory Affairs Benelux Aspen Pharma Group 2023-07-07 Belgium Job Ref #: AP-4195 Industry: Pharmaceutical And Medical/Healthcare Job Type: Permanent Positions Available: 1 Applications are invited for the above indicated vacancy t ...

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📑 **The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.** **• Prov ...

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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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📑 Job Description Keyrus Life Science is looking on a regular basis for Regulatory Affairs Consultants to join our consulting team for clients (from big pharma to small biotech) projects based in Belgium. This job description is an example on how your job could look like. Once we have a specifi ...

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📑 For our Diabetes Care division, we are recruiting a Senior Regulatory Specialist for Benelux. The Senior Regulatory Specialist is responsible for managing an efficient program to ensure that all regulatory activities for Abbott Diabetes Care products are achieved to an agreed schedule. Role and Responsibilities ...

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📑 Position description Category OPERATIONS - ENGINEERING/PRODUCTION Job title R&D Scientist Contract Permanent contract Contractual hours Part-time Job description ...

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📑 You manage the regulatory activities for a diverse range of products, including but not limited to: prepare, submit and follow-up regulatory submissions (BLA, CTD, NDA,…), assess post-approval changes, manage responses to the Board of Health, review of packaging/inserts… You collaborate closely with the Regulatory Affairs team and o ...

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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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📑 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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📑 Job description As a member of our pharmaceutical consulting team, you will play a crucial role in ensuring the quality of pharmaceutical products and processes for our clients. You will be responsible for ensuring compliance with regulatory standards and good manufacturing practices (GMP), while ...

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📑 As the successful Regulatory Affairs Specialist, you will have the following responsibilities:Play a key role in the regulatory information flow and follow-up on registration & compliance projects focussing on EuropeCollect needed scientific data, prepare regulatory & risk assessments, registration dossiers, MSDS, an ...

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📑 Job Description Keyrus Life Science is looking on a regular basis for Technical Regulatory CMC Writers to join our consulting team for clients (from big pharma to small biotech) based in Belgium . This job description is an example on how your job could look like. Once we have a spec ...

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📑 Clinical Project Management services provides local management of a clinical trial (or Medical Affairs data generation activity) across Belgium. Services/deliverables include operational oversight of assigned protocols at the country level from start-up through to database lock and closeout activities. Further, services will ensure the local trial ...

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📑 Position description Category OPERATIONS - ENGINEERING/PRODUCTION Job title Regulatory Affairs Consultant Contract Permanent contract Job description ABOUT US Akkodis is ...

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📑 Position description Category OPERATIONS - ENGINEERING/PRODUCTION Job title Validation Support/Engineer - Life Sciences Contract Permanent contract Contractual hours Full time < ...

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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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📑 The Scope 3HR.be is the Recruitment Partner of Entrepreneurs & small companies, do you like working in such a business with a family ambiance? Our client is a Belgian Engineering office active in various Life Science Industries like Pharmaceutical, Biotechnology, Medical Devices, with expertise in Qu ...

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📑 **Clinical Research Associate** IQVIA Belgium is looking for talented and motivated team member to join our Sponsor dedicated team as junior CRA. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a me ...

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📑 The Scope Our client is a new Engineering office active in various Life Science Industries like Pharmaceutical, Biotechnology, Medical Devices, with expertise in Qualification & Validation, Quality Assurance, Consulting, Engineering and Construction Management.With a constant evolving team composed 25 employees/fr ...

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📑 The Scope Our client is a new Engineering office active in various Life Science Industries like Pharmaceutical, Biotechnology, Medical Devices, with expertise in Qualification & Validation, Quality Assurance, Consulting, Engineering and Construction Management. With a constant evolving team composed 25 employees/freel ...

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📑 Job Location Brussels Job Description Want to work in a role that supports the safety and wellbeing of consumers worldwide? Do you enjoy operating within a growing, dynamic, highly skilled team, working with multiple functions and being part of something bigger than yourself? If so, ...

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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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📑 The Scope 3HR.be is the Recruitment Partner of Entrepreneurs & small companies, do you like working in such a business with a family ambiance?Our client is a Belgian Engineering office active in various Life Science Industries like Pharmaceuti ...

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📑 As a successful Regulatory Affairs Specialist - Pharma - BeNeLux you will have the following responsibilities:Prepare, submit, maintain and record technical and regulatory documentationEnsure up to date EMEA document management systemCollect information on products to create and update the product regulatory informa ...

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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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📑 **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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📑 **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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📑 Scientific and Regulatory Affairs Specialist Corporate division Location: Brussels or Hoofddorp About L’Oréal L'Oréal has been a world leader in the cosmetics business for more than years and has grown into one of the largest FMCG companies in the world. With international bran ...

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📑 For our Diabetes Care division, we are recruiting a Senior Regulatory Specialist for Benelux. The Senior Regulatory Specialist is responsible for managing an efficient program to ensure that all regulatory activities for Abbott Diabetes Care products are achieved to an agreed schedule. Role and Responsibilities: For ...

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📑 When our values align, there's no limit to what we can achieve. Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role ...

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📑 When our values align, there's no limit to what we can achieve. Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team! This is a client dedicated project, and the role ...

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📑 Job Description Our client is a global medical device company, a pioneer of the MR-guided focused ultrasound technology which is a game-changing innovation. They are looking for a Clinical Affairs Program Manager Europe. The role is % remote with up to 40% travel and based in Europe. As part of the global cl ...

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📑 Job Title: Ecotoxicologist City, Country: Louvain la Neuve, Belgium Hybrid/Remote/On Site/: Hybrid As Scientist/Ecotoxicologist, you are the scientific expert assessing and ensuring the environmental safety of dsm-firmenich ingredients in particular from the perfumery & beauty business acc ...

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📑 Job Summary As member of the EMEA Regulatory Affairs (RA) department, the main responsibility of the RA Officer is to provide and coordinate regulatory support for database systems and to remain updated on applicable legislation & standardisation with specific focus on database systems. The RA Officer, will act as ...

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📑 The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.• ...

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📑 For the expansion of our Bioanalytical team, argenx seeks a highly motivated Senior Scientist in Bioanalytics with specialized expertise in immunogenicity assay development/validation for large molecules and/or clinical immunogenicity risk assessment and data interpretation.Operating under an outsourced model, argenx collaborates with bio ...

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📑 Regulatory Affairs Expert in Animal Health – Pharmaceuticals – Brussels – 12 Months Do you want to be involved with exciting Pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of E ...

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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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📑 We are currently seeking a Clinical Scientist for a remote position with one of our clients. If you possess a background aligned with the requirements of this role and find it intriguing, we encourage you to apply.Location: Europe (Remote, Team based in Belgium) Duration: 1.5 years Salary: €70,000 - €100,00 ...

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📑 RESPONSIBILITIES : - Guidance to some customers on the regulatory requirements - Writing, preparation of dossier for regulatory submissions like ANDA, Type B/C, BLA, Breakthrough Designation, Interact/fastrack,... - Writing and submission of the pre-IND and/or IND, in close collaboration with the custom ...

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📑 Responsibilities As a Associate Regulatory Site Officer you are responsible for managing and reviewing of CMC (Chemistry, Manufacturing and Controls) dossiers, variations, renewals, annual reports, site registrations and territory extensions as part of regulatory product lifecycle management responsibility ...

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📑 At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innova ...

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📑 Functie Het landschap van de gezondheidszorg en de medische industrie heeft de afgelopen jaren heel wat positieve ontwikkelingen gekend. Deze sectoren worden voortdurend uitgedaagd om verder te evolueren. Meer dan ooit hebben ze nood aan specifieke profielen die een toegevoegde waarde bieden en innovatieve ide ...

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📑 argenx is actively seeking a highly motivated Senior Scientist in Bioanalytics to join our expanding Bioanalytical team. The ideal candidate will possess extensive expertise in biomarker assay development and validation for large molecules.Operating under an outsourced model, argenx collaborates with bioanalytical vendors. The Senior Scie ...

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📑 You ensure that the manufacturing processes comply with the GMP regulations. You develop, implement and maintain quality systems such as QMS, QCS, and SOPs to ensure the consistent production of high-quality products. You conduct risk assessments and perform root cause analysis, striving for continuous improvement < ...

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📑 At Johnson & Johnson,we believe health is everything.Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to inno ...

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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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📑 Introduction For our client in Zaventem we are looking for a SR. Associate Regulatory Affairs s who will provide regulatory guidance and support for regional and global veterinary biological maintenance teams and development project teams. Job description The Sr Asso ...

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📑 Regulatory Affairs Officer Global Registrations Animal Health Human Health Contract Manufacturing Belgium Over KELA KELA, opgericht in , is een Belgische farmaceutische bedrijvengroep. KELA is een betrouwbare ontwikkelaar, producent en verdeler van veterinaire ...

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📑 Position description Job title Internship Audit Function Audit - Intern Roles & Responsibilities #Audit #Economics #KPMG #Stage#Trainee#Intern The fundamental role of an auditor is to report to the shareholders ...

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