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📑 Meda Pharma GmbH & Co KG At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access – Providing ...

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📑 Head of Regulatory CMC Germany (f/m/d) Das erwartet Sie In dieser Schlüsselposition leiten Sie die deutschen Regulatory CMC Abteilungen, setzen globale Geschäftsentwicklungsinitiativen in operative Maßnahmen um und optimieren die Entwicklung der Regulatory CMC-Services in Deutschland. Als Business-Pa ...

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📑 This position can be fully remote Global Regulatory experience needed. Demonstrated project management experience needed. PURPOSE AND SCOPE: Ensures company products meet regulatory requirements by supporting all assigned regulatory aspects of product approval and post-marketing compliance. Develops, ...

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📑 In your role as Regulatory Affairs Manager (m/f/d) you will support product registrations, provide design input and assess changes to ensure regulatory product availability on global markets. Your assignments: Obtain and sustain global registrations for product portfolio as per Regulatory Strategy and product roadmap <li ...

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📑 The ideal candidate should have US Advertising and Promotion experience. This position can be fully remote. PURPOSE AND SCOPE: Ensures company products meet regulatory requirements by supporting all assigned regulatory aspects of product approval and post-marketing compliance. Develops, coordinates, reviews a ...

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📑 Your Tasks: Definition, maintenance and further development of processes to ensure regulatory compliant approval of FME medical devices worldwide Creation and provision of regulatory documents for the global registration of FME medical devices Consulting and supporting all involved parties in the ...

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📑 PURPOSE AND SCOPE: Develops regulatory strategies for assigned products/product lines. Prepares regulatory submissions required to market new or modified medical devices in the domestic and international clinical markets. Develops and maintains procedures and systems designed to ensure the product development process addresses ...

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📑 Key Roles and Responsibilities: Conducting risk assessments and developing risk registers. Reviewing and updating policies and procedures to ensure compliance with regulatory requirements. Monitoring regulatory changes and assessing their impact on the organization. Collaborating with cro ...

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📑 Für unser Verifikations-Team suchen wir zum nächstmöglichen Zeitpunkt Unterstützung. Unbefristet - Vollzeit - Flexibles Arbeitszeitmodell - Mobiles Arbeiten teilw. möglich - Wir freuen uns sehr auf Ihre Bewerbung. We are looking for support for our verification team as soon as possible. Permanent - Full-time - Flexible wor ...

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📑 Fresenius Medical Care is the world’s leading provider of products and services for individuals with renal diseases of which around 3.9 million patients worldwide regularly undergo dialysis treatment. We care for more than 344,000 dialysis patients and provide our products in around 150 countries. With a strong focus on innovation, qua ...

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📑 Position Purpose: The holder of this position reports to the Senior Legal Counsel based in Bad Homburg, Germany and acts as a strategic legal partner to the various businesses of the Medical Technology division by providing practical and business-oriented guidance on healthcare regulatory, commercial, government policy, enforc ...

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📑 PURPOSE AND SCOPE: The System Owner will report into Quality Management and Regulatory Systems Head (QMRS) and will be responsible for overseeing the implementation and maintenance of Quality Management System (QMS) software solutions, including Regulatory Information Management (RIMs) and Regulatory Intelligence (RI) systems ...

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📑 Main tasks: Material compliance: Evaluation of raw materials as well as finished products concerning regulatory EHS-requirements on substances and materials (REACH, POP, MDR, CLP, Packaging Directive etc.) Contact person to external supplier concerning the before mention ...

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📑 Are you excited about clinical evaluation and would you like to look behind the scenes of the Medical Systems Products department to gain experiences in an international company during your studies? Then join our team and support us in regulatory tasks in a friendly environment. You will have the opportunity to get actively involved in our dail ...

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📑 Regulatory Affairs Manager (m/w/d) Anstellung bei der Hays Professional Solutions GmbH in Bad Homburg Startdatum: sofort Referenznummer: 487340/1 Diesen Job teilen oder drucken Ihre Aufgaben Erstellung, Erhalt, Pflege und Einreichung von Zulassungen für Arzn ...

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📑 Mylan Germany GmbH At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access – Providing high ...

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📑 Beschreibung der GesellschaftDQS MEDIZINPRODUKTE GMBHLERNEN SIE UNS KENNENAnspruchsvoll. Kompetent. Dynamisch: So verstehen wir, die DQS Medizinprodukte, uns und die Dienstleistungen für unsere Kunden. Wir bündeln weltweit unser Know-how rund um die Zertifizierung und Notifizierung von Managementsystemen und Pro ...

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📑 Main tasks: Material compliance: Evaluation of raw materials as well as finished products concerning regulatory EHS-requirements on substances and materials (REACH, POP, MDR, CLP, Packaging Directive etc.) Contact person to external supplier concerning the before mention ...

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📑 Your Job Ensure vendor/supplier qualifications are carried out in line with company policy and procedure Work cross functionally to resolve supplier related issues and drive continuous improvement Complete vendor/supplier questionnaires on behalf of the QA function against agreed timeframes <l ...

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📑 PURPOSE AND SCOPE: Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatm ...

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📑 Your Tasks: Creation and maintenance of non-clinical documentation for medicinal products, e.g., CTD modules 2.4 and 4 in alignment with Global Drug Regulatory Affairs and other relevant stakeholders Responsibility for the content of the above-mentioned regulatory information (subject matter e ...

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📑 Mylan Germany GmbH At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access – Providing high ...

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📑 Description : Toxicology Manager Role Overview: Huntsman Corporation’s Product Safety and Regulatory Compliance Team is searching for an experienced Toxicology Manager. As a Toxicology Manager at Huntsman, you will lead a global, dynamic team of eight toxicologists, fostering a cultu ...

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📑 In your role as Assistant Medical, Safety & Post Market Surveillance (m/w/d) you will be responsible for effective administrative support for the supervisors and managers of the System, Quality and Regulatory department with a focus on the Medical, Safety & PMS department. Your tasks Planning and coordination of inte ...

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📑 Caring for People's Health as a Trusted Partner - This mission motivates us at STADA every day to improve the health of people worldwide. With our wide range of generics, consumer health products and specialty pharmaceuticals, we offer patients, doctors and pharmacists a wide range of therapeutic options. Around 11,700 employees live o ...

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📑 Junior Expert (m/w/d) Regulatory Affairs - Labeling Innerhalb von Fresenius Medical Care hat Regulatory Affairs die Hauptverantwortung dafür, dass das Unternehmen seine Zulassungen für Medizinprodukte und Arzneimittel erhält und aufrechterhält. Tragen Sie Ihren Teil dazu bei und sorgen Sie für die perfekte Aufmachung ...

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📑 PURPOSE AND SCOPE: The System Owner will report into Quality Management and Regulatory Systems Head (QMRS) and will be responsible for overseeing the implementation and maintenance of Quality Management System (QMS) software solutions, including Pharmacovigilance (PV) and Complaints. The System Owner will also be responsible for ensurin ...

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📑 Project Support Medical Device Regulation for irrigation solutions (m/f/d) Employment with Hays Professional Solutions GmbH Bad Homburg Start date: asap Reference number: 514994/1 Diesen Job teilen oder drucken Your responsibilities MDR Remediation of design ...

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📑 Caring for People's Health as a Trusted Partner - This mission motivates us at STADA every day to improve the health of people worldwide. With our wide range of generics, consumer health products and specialty pharmaceuticals, we offer patients, doctors and pharmacists a wide range of therapeutic options. Around 13,000 employees live o ...

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📑 PURPOSE AND SCOPE: Acts as a serving leader to direct, administer and oversee the day to day operations and activities of dialysis facilities and programs within a specified and potentially changing geographic proximity. The scope includes, but is not limited to, chronic in-center clinics and home therapy programs, in an assi ...

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📑 PURPOSE AND SCOPE: Directs and grows a dialysis business within a defined region through effective leadership and management of all aspects of customer service, quality patient care, marketing and responsible financial management. Practices cost containment strategies, maintaining profitability and growth while ensuring compl ...

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📑 PURPOSE AND SCOPE: Entry level position focuses on the development of Knowledge, Skills, and Abilities (KSA) in a supervised environment with the intent of developing performance and effective, efficient independent functioning under close supervision upon completion of various training processes over time. Under close supervision and ...

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