Lavori attuali relativi a Regulatory Affairs Manager - Milano - Meet Recruitment Limited
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Senior Regulatory Affairs Manager
2 settimane fa
Milano, Lombardia, Italia Cpl Healthcare A tempo pienoJob Title: Senior Regulatory Affairs ManagerJob Type: Full Time, Permanent PositionLocation: Italy (Milan) – HybridRemuneration: Attractive salary and packageCpl Healthcare is seeking a Senior Regulatory Affairs Manager to join our team. As a key member of our Regulatory Affairs department, you will be responsible for the strategic lifecycle management of...
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Regulatory Affairs Manager
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Milano, Lombardia, Italia W Executive S.R.L. A tempo pienoJob Description: We are seeking a highly skilled Regulatory Affairs Manager to join our team at W Executive S.R.L. The successful candidate will be responsible for ensuring that all our products meet the relevant government legislation and regulations, while prioritizing patient safety and efficacy. The main responsibilities of this role include:Managing the...
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Regulatory Affairs Specialist
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Milano, Lombardia, Italia The Kraft Heinz Company A tempo pienoJob Title: Regulatory Affairs ManagerJob Summary:We are seeking a highly skilled Regulatory Affairs Manager to join our team at The Kraft Heinz Company. As a key member of our Legal, Government and Regulatory department, you will be responsible for ensuring all product labels comply with food legislation and company policies.Key Responsibilities:Ensure...
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Regulatory Affairs Specialist
3 settimane fa
Milano, Lombardia, Italia The Kraft Heinz Company A tempo pienoJob Title: Regulatory Affairs ManagerJob Summary:We are seeking a highly skilled Regulatory Affairs Manager to join our team at The Kraft Heinz Company. As a key member of our Legal, Government and Regulatory department, you will be responsible for ensuring all product labels comply with food legislation and company policies.Key Responsibilities:Ensure...
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Regulatory Affairs Specialist
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Milano, Lombardia, Italia The Kraft Heinz Company A tempo pienoJob Title: Regulatory Affairs ManagerJob Summary:We are seeking a highly skilled Regulatory Affairs Manager to join our team at The Kraft Heinz Company. As a key member of our Legal, Government and Regulatory department, you will be responsible for ensuring all product labels comply with food legislation and company policies.Key Responsibilities:Ensure...
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Regulatory Affairs Specialist
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Milano, Lombardia, Italia W EXECUTIVE S.R.L. A tempo pienoJob Title: Regulatory Affairs ManagerW EXECUTIVE S.R.L. is seeking a highly skilled Regulatory Affairs Manager to join our team. As a key member of our organization, you will be responsible for ensuring that our products meet all relevant regulatory requirements and standards.Key Responsibilities:Develop and execute regulatory strategies and plans to ensure...
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Regulatory Affairs Specialist
2 settimane fa
Milano, Lombardia, Italia W EXECUTIVE S.R.L. A tempo pienoJob Title: Regulatory Affairs ManagerCompany: W EXECUTIVE S.R.L.Location: MilanoAs a Regulatory Affairs Manager at W EXECUTIVE S.R.L., you will be responsible for ensuring that our company's products comply with all relevant laws and regulations. This includes developing and executing regulatory strategies, managing product registrations, and providing...
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Regulatory Affairs Specialist
1 mese fa
Milano, Lombardia, Italia W EXECUTIVE S.R.L. A tempo pienoRegulatory Affairs ManagerW EXECUTIVE S.R.L. is seeking a highly skilled Regulatory Affairs Manager to join our team. As a key member of our organization, you will be responsible for ensuring that our products meet all relevant regulatory requirements and standards.Key Responsibilities:Develop and execute regulatory strategies and plans to ensure compliance...
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Regulatory Affairs Expert
24 ore fa
Milano, Lombardia, Italia The Kraft Heinz Company A tempo pienoJob Title: Regulatory Affairs ManagerJob Summary:We are seeking a highly skilled Regulatory Affairs Manager to join our team at The Kraft Heinz Company. As a Regulatory Affairs Manager, you will be responsible for ensuring all product labels used by Kraft Heinz in Europe comply with food legislation, government guidelines, and company policies, with a...
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Regulatory Affairs Director
1 settimana fa
Milano, Lombardia, Italia Cpl Healthcare A tempo pienoJob Title: Associate Director, Regulatory Affairs - Medical Device/Post Market SurveillanceJob Type: Full Time, Permanent PositionLocation: HybridRemuneration: Attractive salary and packageCpl Healthcare is seeking an experienced Associate Director, Regulatory Affairs - Medical Device Lifecycle Management to join their team. This role offers a unique...
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Regulatory Affairs Specialist
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Milano, Lombardia, Italia PharmaLex A tempo pienoAbout the JobWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at PharmaLex. As a Regulatory Affairs Specialist, you will be responsible for managing the preparation and revision of informative texts for healthcare professionals and patients, as well as ensuring compliance with regulatory requirements.Your...
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Regulatory Affairs Director
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Milano, Lombardia, Italia Parexel A tempo pienoRegulatory Affairs Director Job DescriptionWe are seeking a highly skilled and experienced Regulatory Affairs professional to lead our team's regulatory efforts. As a Director, you will be responsible for ensuring compliance with regulatory requirements and guidelines, providing guidance to project teams, and managing performance and development of staff...
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Regulatory Affairs Manager
4 mesi fa
Milano, Italia Pharmalex A tempo pieno**We are growing, grow with us!** Are you looking for a dynamic company with daily challenges and opportunities? Then, Pharmalex is your next career move! Pharmalex is one of the leading service companies for the Pharmaceutical Industry globally, specialised in all aspects of drugs and medical devices approval of the market development, and any action of...
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Regulatory Affairs Expert
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Milano, Lombardia, Italia Parexel A tempo pienoJoin Our Team as a Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience, project management...
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Regulatory Affairs Expert
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Milano, Lombardia, Italia Parexel A tempo pienoUnlock Your Potential in Regulatory AffairsParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience, project...
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Regulatory Affairs Director
2 settimane fa
Milano, Lombardia, Italia Cpl Healthcare A tempo pienoJob Title: Associate Director, Regulatory Affairs - Medical Device/ Post Market SurveillanceJob Type: Full Time, Permanent PositionLocation: HybridRemuneration: Attractive salary and packageCpl Healthcare is seeking an experienced Regulatory Affairs Director to join their team. The ideal candidate will have a sound understanding of new registrations and...
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Regulatory Affairs Specialist
6 giorni fa
Milano, Lombardia, Italia Hover Senior Living Community A tempo pienoJob SummaryThe Regulatory Affairs Senior Specialist will be supporting the implementation, execution and management of the local regulatory activities in Italy ensuring regulatory compliance with local regulatory requirements and corporate policies.The Regulatory Affairs Senior Specialist supports interactions with the national Regulatory Authorities, i.e....
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Regulatory Affairs Specialist Eu
5 mesi fa
Milano, Italia Clinglobal Group A tempo pieno**Regulatory Affairs Specialist - European Union** Clinglobal is an Animal Health Contract Research Organisation and supports our global operations in various countries. We are currently looking for a** Regulatory Affairs Specialist** based in the EU to join our growing Regulatory Affairs team at Clinglobal. This position offers the opportunity to work...
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Regulatory Affairs Specialist
3 settimane fa
Milano, Lombardia, Italia Pfizer, S.A. De C.V A tempo pieno{"title": "Regulatory Affairs Specialist", "content": "Job SummaryPfizer is seeking a highly skilled Regulatory Affairs Specialist to join our team in the EU region. As a key member of our Global Regulatory Strategic Team, you will be responsible for providing regional strategic expertise and leading EU regulatory strategies for assigned projects and...
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Regulatory Affairs Cmc
5 mesi fa
Milano, Italia HAYS A tempo pienoAzienda Farmaceutica - Affari Regolatori - Regulatory Affairs CMC - GMP La tua nuova aziendaIl nostro cliente è una realtà multinazionale che produce e commercializza prodotti farmaceutici generici.Il tuo nuovo ruoloIn ottica dell’ampliamento dell’organico, siamo alla ricerca di una figura di Regulatory Affairs CMC.La risorsa risponderà direttamente...
Regulatory Affairs Manager
2 mesi fa
Global Regulatory Affairs ManagerWe're currently seeking a Global Reg Affairs Manager for an award-winning pharma company specialising in OTC products.
Overseeing the whole dossier process, working with license variations, acting as a submission specialist will all be core components of this roleThe Regulatory Affairs Manager will be responsible for overseeing the regulatory process for products, from development to post-market approval.
He/she will ensure compliance with applicable regulations and standards.RESPONSIBILITIESPreparation (compile and/or write the modules of an eCTD file, mainly Module 1 and 3), review and submission of regulatory documents throughout the product lifecycle (initial marketing authorisation submission, variations, notifications and renewals) to regulatory agencies to ensure timeliness, accuracy, comprehensiveness, or compliance with regulatory standardsPreparation, review and submission of responses to regulatory agency inquiriesMonitor and set timelines for licence variations, notifications and renewal approvalsEnsure compliance with regulatory requirements and guidelinesMonitor and update regulatory documentation as necessary to keep company in compliance from a regulatory perspectiveParticipate in meetings with regulatory agencies as neededParticipate in meetings with manufacturers as neededAdvise manufacturers on regulatory requirementsDocument and track regulatory submissions and regulatory authority approvalIs responsible for review, proof reading and approval of artwork of packaging materials to ensure compliance with regulatory requirementsIs responsible for the preparation of Summary of Product Characteristics, Patient Information Leaflets and labelling according to the Quality Review Documents (QRD) formatCollaborate with cross-functional teams including RD, Quality, and Marketing to ensure that all regulatory requirements are met throughout the product lifecycleProvide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of productsKeep up to date with national and international legislation, guidelinesMaintains RA archives (electronically)EXPERIENCE PROFILEScientific background is a must – master's degree in pharmaceutics, health care, life sciences or related fields preferred5 + years of experience in a similar role, preferably in an international environmentMinimum of 5 years of experience in regulatory affairs within the pharma industryA good knowledge and preferably experience with pharmaceutical development and validation of processesExperience in developing and maintaining regulatory compliance documentation, including technical files, regulatory dossiers, and other relevant documentationExperience in interacting with regulatory authoritiesExcellent planning and time management skillsA good knowledge of relevant European guidelines, applicable legislation and regulationsFluent communication skills in English (written and oral), also in Dutch is an assetCOMPETENCIESStrong team player, with the ability to work effectively in team setting and interaction with people of different seniority and functional backgroundsAbility to work independently and as part of a teamAbility to offer ideas and accept ideas of othersHighly ethical, honestly, reliability, accountability, loyaltyAbility to handle and enjoying complex and changing environmentsPositive "can do" attitudeAbility to consistently meet deadlines, remain organized, adaptable and autonomousGood communication and presentation skillsEnglish language skills (spoken and written), Dutch is a bonusAbility to work concurrently on projects, each with specific instructions that may differ from project to projectIf this role sounds interesting to you, then please apply or reach out to ****** #J-18808-Ljbffr
