Regulatory Affairs Cmc Manager

Vor 3 Tagen


Zurich, Schweiz CSL Behring Vollzeit

CSL Vifor is a world leading Nephrology, Iron Deficiency and Cardio-Renal pharmaceutical company. We are experiencing rapid growth due to pipeline realization, optimization and innovative alliance partnerships on a global basis.
- Effectively collaborate with technical experts, oversee and direct compilation and update of CMC related dossier components, pro-actively provide input to project planning, evaluation and decision making, and address CMC regulatory questions related to the assigned product(s).
- Evaluate available technical and scientific CMC information for compliance with relevant regulatory requirements, perform gap analysis and propose solutions and strategies to remediate risks.
- Lead the timely provision of compliant global regulatory impact assessments for planned CMC changes.
- Liaise with relevant GRA sub-functions (Product Strategy, International Strategy, LCM) to initiate and oversee the development and implementation of regulatory submission plans for CMC changes and ensure they are suitable to meet business goals.
- Author and manage regulatory CMC documentation in compliance with applicable regulations, and internal procedures, workflows and systems.
- Promote knowledge sharing and development of regulatory expertise within Regulatory Affairs CMC.
- Contribute to the development or improvement and training of regulatory policies and procedures.

**Minimum Requirements**
- MA/MS or equivalent university degree in natural or life sciences
- Minimum of 5 years’ experience in the biotech or pharmaceutical industry, with at least 3 years in Regulatory Affairs, Quality, Pharmaceutical Development or other relevant area.
- Solid technical regulatory expertise.
- Demonstrated understanding of the regulatory framework in at least one key region (US, EU, CH, Japan, China).
- Fluency in English (verbal and written).

**Additional Qualifications**
- Ph.D. or further degree, e.g. in Regulatory Affairs
- Knowledge in Good Manufacturing Practice or Quality Management
- Good command of German (verbal and written).
- Strong team player with a demonstrated ability to develop constructive and effective relationships and successfully influence across all levels of the organization to achieve business goals.
- Thinks solution-oriented and takes a proactive approach in identifying business needs, facilitating information flow and developing new creative approaches.

**About CSL Vifor**:
CSL Vifor aims to become the global leader in iron deficiency and nephrology.

The company is a partner of choice for pharmaceuticals and innovative patient-focused solutions across iron, dialysis, nephrology and rare conditions. CSL Vifor strives to help patients around the world with severe, chronic and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision patient care.

**We want CSL to reflect the world around us**:
As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.

**Do work that matters at CSL Vifor**:



  • Zurich, Schweiz NonStop Consulting Vollzeit

    Regulatory Affairs Manager role - Switzerland (German) - CMC I am currently looking for an experienced Regulatory affairs manager, CMC to join a good reputation employer in a German canton of Switzerland. In your role you will be responsible for all CMC aspects, providing strategic and operational guidance to different teams in order to ensure achieving the...


  • Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    Join Takeda as a Director, Global Regulatory Affairs (GRA) CMC, where you will lead GRA CMC Due Diligence in partnership with organizational and external stakeholders. You will ensure the communication/development of regulatory CMC risks and strategy, develop best practices that enable CMC due diligence, ensuring that a given compound meets technical and...


  • Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as an Associate Director, Global Regulatory Affairs CMC - Marketed Products in our Zurich office. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As an...


  • Zurich, Schweiz NonStop Consulting Vollzeit

    If a chance to maximise the regulatory approvals with the use of your expertise and experience in RA sounds like something you would like to pursue, this position is for you! **Your responsibilities will be**: Establishing a coherent process and maintaining transparent communications between Global CMC and Regional Regulatory teams to enable CMC regulatory...


  • Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as an Associate Director, Global Regulatory Affairs CMC - Marketed Products in our Zurich office. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As an...


  • Zurich, Schweiz Takeda Vollzeit

    At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Director,...


  • Zurich, Schweiz Takeda Vollzeit

    Join Takeda as Associate Director, Global Regulatory Affairs CMC Established Products Inspired Collaboration (EPIC) Lead, where you are accountable for developing and executing on GRA CMC strategies for lifecycle management. You ensure global strategies are implemented across existing portfolio, while ensuring team effectiveness in a complex matrix...


  • Zurich, Schweiz Takeda Vollzeit

    Join Takeda as Director, Global Regulatory Affairs CMC Alliance Partnered and Divested Product Lead, where you are accountable for developing and executing on GRA CMC strategies for lifecycle management. You ensure global strategies are implemented across existing portfolio, while ensuring team effectiveness in a complex matrix environment. Reporting to the...


  • Zurich, Schweiz Pfizer Vollzeit

    **Regulatory Affairs Manager (M/F)** **Contract limited** **This is what you can look forward to**: - Overseeing assigned product portfolio of innovative prescription drugs with complex regulatory background - Handling entire regulatory lifecycle from initial MAAs to line extensions, labeling and CMC variations, renewals, PSUR submissions, etc. -...


  • Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    **People First** - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. **Our people are the heart of Takeda.** Our team is growing and for this we need bright minds with creativity and flexibility - what talent do...


  • Zurich, Schweiz Bernwald Personalberatung Vollzeit

    Unsere Mandantin ist ein Schweizer KMU, das sich in einer Nische im Pharmabereich erfolgreich etabliert hat. - In ihrem Auftrag suchen wir eine Persönlichkeit mit ausgeprägtem Verantwortungsbewusstsein als Regulatory Affairs Manager Pharma EU/CH (m/w/d). **IHRE AUFGABEN**: - Selbständiges Erstellen von CMC-Zulassungsdokumentationen - Termingerechte...


  • Zurich, Schweiz Experis Vollzeit

    **Manager Regulatory Affairs** Experis IT is on the search for a **Manager Regulatory Affairs** to join one of their clients, a well-known international pharma company based in Switzerland. **Contact**:Francesca De Chirico **Start Date: ASAP** **Duration**:12** **M**onths** **Location**:Zürich** **Workload percentage**:100%** **Hybrid Model** **Key...

  • Regulatory Affairs

    Vor 5 Tagen


    Zurich, Schweiz two.jobs Vollzeit

    For our Client Selectchemie AG we are looking for a Regulatory Affairs (CMC) Associate (100%) Finished Dosage Forms. About Selectchemie AG Selectchemie AG is an independent Swiss company and since 1969 a first class distributor and service provider for the global Pharma and Swiss Nutrition industries. As exclusive distributor for leading suppliers of raw...


  • Zurich, Schweiz Sonova Vollzeit

    Who we are You enjoy creating and innovating. You never stop striving for better. You take responsibility and you get results. You love being part of a team. Above all, you want your work to matter: Welcome to our world! At Sonova we create sense by bringing sound to life. Our innovative hearing care solutions help millions of people enjoy life’s...


  • Zurich, Schweiz Advanced Bionics Vollzeit

    Who we are You enjoy creating and innovating. You never stop striving for better. You take responsibility and you get results. You love being part of a team. Above all, you want your work to matter: Welcome to our world! At Sonova we create sense by bringing sound to life. Our innovative hearing care solutions help millions of people enjoy life’s...

  • Ra Manager

    vor 1 Woche


    Zurich, Schweiz BioTalent Vollzeit

    BioTalent are partnered with an exciting company to assist their search for a newly created Regulatory Affairs Manager on a permanent basis as part of their ongoing growth plans. **Key Responsibilities**: - Maintain the approved dossiers of the lifecycle of the products - Ensure that Regulatory procedures and records with respect to CMC / Quality are in...


  • Zurich, Schweiz Pfizer Vollzeit

    Weltweit arbeiten die Mitarbeiter von Pfizer gemeinsam daran, die Gesundheit eines jeden Einzelnen überall zu verbessern. Während wir Arzneimittel und Medizin-Produkte entwickeln und unser Geschäft global ausweiten, halten wir jederzeit Ausschau nach neuen Talenten. Derzeit suchen wir Sie an unserem **Standort in Zürich **als: Regulatory Affairs...


  • Zurich, Schweiz LHH Vollzeit

    Für unseren Mandanten mit Niederlassung im Grossraum Zürich suchen wir einen **Regulatory Affairs Manager (m/w/d)**. Ein familiärer Umgang und eine täglich gelebte Wertschätzung zeichnen das Unternehmen aus. Aufgabengebiet - Mitarbeit in Projektteams und Schnittstelle zu anderen Fachabteilungen hinsichtlich der regulatorischen Anforderungen bei der...


  • Zurich, Schweiz Pfizer Vollzeit

    Weltweit arbeiten die Mitarbeiter von Pfizer gemeinsam daran, die Gesundheit eines jeden Einzelnen überall zu verbessern. Während wir Arzneimittel und Medizin-Produkte entwickeln und unser Geschäft global ausweiten, halten wir jederzeit Ausschau nach neuen Talenten. Derzeit suchen wir Sie an unserem Standort in Zürich als: Regulatory Affairs Coordinator...


  • Zurich, Schweiz CSL Behring Vollzeit

    CSL Vifor is currently undergoing unprecedented growth and portfolio expansion within rare diseases, Nephrology and Cardiorenal therapeutic areas. A permanent global position in the Global Regulatory Affairs Labelling team has arisen. Which can be based at any of our CSL R&D Hubs (Maidenhead UK, Amsterdam, NL, Bern, CH, Zurich, CH, KOP, PA or Waltham,...