Aktuelle Jobs im Zusammenhang mit QA/ra Associate - Zurich - Hays

  • QA/ra Associate

    vor 2 Wochen

    Zurich, Schweiz Panda Vollzeit

    At this moment, I am looking for a QA/RA manager to join a dynamic MedTech scale-up in Zurich. This organisation is on an inspiring mission in the healthcare industry by improving the quality of care and they’re currently in an exciting phase of growth. In this role, you’ll bring QA/RA to the next level by joining the QA/RA department. Next to that,...

  • Head of QA/ra

    vor 2 Wochen

    Zurich, Schweiz Panda Vollzeit

    At this moment, I am looking for a QA/RA manager to join a dynamic MedTech scale-up in Zurich. This organization is on an inspiring mission in the healthcare industry by improving the quality of care and they’re currently in an exciting phase of growth. In this role, you’ll bring QA/RA to the next level by leading the QA/RA department. Next to that,...

  • Associate Director, Eucan Regulatory Lead, Gi

    vor 2 Wochen

    Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an** **Associate Director, EUCAN Regulatory Lead, GI in Zurich. **Here, you will be a vital contributor to our inspiring, bold mission.** **OBJECTIVE**: - Collaborates to define, develop and lead regional strategies to maximize...

  • Associate Director, Global Regulatory Affairs Cmc

    vor 1 Woche

    Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine?Join us as an **Associate Director, Global Regulatory Affairs CMC** based in Zurich. **Here, you will be a vital contributor to our inspiring, bold mission.** **OBJECTIVE**: - Responsible and accountable for regulatory CMC development,...

  • Director/associate Director, Eu Regulatory Lead

    Vor 5 Tagen

    Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a **Director/Associate Director, EU Regulatory Lead - Rare Genetic & Hematology** in our **Zurich **office. **Here, you will be a vital contributor to our inspiring, bold mission.** **Objective**: - Defines, develops and manages...

  • Associate Director, Eucan Regulatory Lead, Oncology

    vor 2 Wochen

    Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    **OBJECTIVE**: - Collaborates to define, develop and lead regional strategies to maximize regulatory approvals and patient access to meaningful medicines in alignment with program objectives. - Effectively communicates objective assessments of the likelihood of success of these regulatory strategies - Provides strategic and tactical advice and guidance to...

  • Associate Director

    Vor 2 Tagen

    Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    Job Description **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**. Looking for an interesting role where you can develop your career, work at a growing...

  • (Associate) Director, Eucan Regulatory Lead, Gi

    Vor 5 Tagen

    Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a EUCAN Regulatory Lead GI in Switzerland. **Here, you will be a vital contributor to our inspiring, bold mission.** **OBJECTIVE**: - Defines, develops and leads regional strategies to maximize regulatory approvals and patient access...

  • Quality Assurance Associate

    vor 1 Woche

    Zurich, Schweiz two.jobs Vollzeit

    For our Client Selectchemie AG we are looking for a Quality Assurance Associate (100%). 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 materials, APIs and...

  • Quality Assurance Associate

    vor 1 Woche

    Zurich, Schweiz two.jobs Vollzeit

    Für unseren Kunden Selectchemie AG suchen wir eine/n Quality Assurance Associate (100%) 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 materials, APIs and...

  • Product Manager, Aladdin Wealth Tech, Associate

    Vor 5 Tagen

    Zurich, Schweiz BlackRock Vollzeit

    Description About this role About this role This product management role will work on Aladdin Wealth Tech’s product capabilities for discretionary portfolio managers (DPM). The individual will help advance our product vision in this area, evolve product/market fit, and drive roadmap planning, development, and delivery. This role will work closely with a...

  • Associate Director Regulatory Affairs, Marketed

    vor 2 Wochen

    Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an **Associate Director, EUCAN (Europe & Canada) Regulatory Affairs **Strategy Lead, Marketed Products **in our **Zurich** office. **Here, you will be a vital contributor to our inspiring, bold mission.** **OBJECTIVE**: -...

  • Associate Director, Pv Vaccine Expert

    vor 2 Wochen

    Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine?Join us as an **Associate Director, PV Vaccine Expert - EUCAN** for our Vaccines Business Unit, based in Zurich, Switzerland. **Here, you will be a vital contributor to our inspiring, bold mission.** **OBJECTIVE**: - Responsible for supporting...

  • Regulatory Affairs Manager

    vor 2 Wochen

    Zurich, Schweiz Takeda Pharmaceutical Vollzeit

    **SUMMARY** Responsible for - ** Regulatory Affairs** Obtain and maintain marketing authorizations for products and communication of general regulatory requirements in support of licensing of Takeda’s products **TASKS AND RESPONSIBILITES** - Manage **MA lifecycle maintenance** for a defined product portfolio, inclusive local impact assessments of global...

  • Head Regulatory Affairs Emerging Markets

    Vor 4 Tagen

    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**. Are you a strategic and visionary leader with a strong background in regulatory affairs within the...

QA/ra Associate

vor 1 Monat

Zurich, Schweiz Hays Vollzeit

**My duties**
- Batch record review and continuous product quality follow-up
- PQR management
- Assessing deviation reports received from CMOs
- Support handling, responding, tracking of complaints received from customers
- Participate in internal and CMO audits incl. CAPA follow-up and (re-)audit coordination
- Evaluate change requests received from CMO/CRO/API manufacturer from a regulatory affairs and GMP point of view
- Initiate internal change requests
- Product dossier updates, review of updates received from CRO/CMO or regulatoryservice providers, identification of deficiencies
- Participate in development of variation submission strategy for finished products
- Track submitted variations in different countries and by different customers
- Keep internal databases updated
- Release of secondary packaging specification
- Release of secondary packaging technical check

**My qualifications**
- Scientific background with a BSc or higher in Life Sciences
- Working experience in a QA- or production-related role at a manufacturing site of medicinal products
- Additional working experience in regulatory affairs tasks of FDF is an asset
- Eager to work within a framework of regulations like GMP/GDP/GxP
- Proficiency in English is a must, knowledge in German is of advantage

**My benefits**
- You will become a member of a highly qualified and motivated FDF & Dossier Business Team. This newly created position is designed to further increase the capacities and gives you the opportunity to strengthen your QA knowledge and to grow into Regulatory Affairs activities. The company offers a great team spirit in an international working environment, which is paired with a Swiss style of doing business like reliability, continuity and quality.

**About Hays**
- With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages - completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.**My contact at Hays**

**Reference number**
626445/1

**Contact**
Phone:
+41 44 225 50 00