Quality Coordinator - VIE Contract
Genzyme Corporation
Vernier
vor 15 Tg.

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.

Therefore, only applications that are submitted in English will be considered.

At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences.

We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.

We are looking for a candidate for a VIE mission of :

Quality Coordinator - VIE Contract (W / M)

Job Details :

The junior product quality manager will be immersed into the main activities of a responsible person in Switzerland learning on the European and Swiss legal requirements applicable to product handling and commercialization.

As key responsibilities, you will have to manage in an autonomous manner :

  • Market batch release, as QP (Quality Procedure) delegate role including deviations and CAPAs (Corrective And Preventive Actions) management linked to releases
  • The returns and destruction process
  • Supervising the product technical complaints
  • Leading assigned change controls in close collaboration with the Swiss Responsible Person
  • Coordinating the entire PQR (Product Quality Review) program for Switzerland in collaboration with our service provider and coordinating a section of the program of Ireland and France, working in partnership with the PQR coordinator of these countries
  • Coordinating the preparation of the regulatory inspection or audits and taking active part in the back office
  • Updating or creating quality agreements with our contract manufacturing organization, external manufacturing entities, Sanofi manufacturing entities or suppliers
  • You will have to manage your priorities and be in constant interactions with Supply Chain, Regulatory affairs, pharmacovigilance departments and business units at country and Multi-

    Country Organization. You will also interact with the corresponding Global Quality functions, when required.

    You will integrate a dynamic, international team and be given the possibility to develop all the necessary skills and knowledge to become a qualified person / responsible person or a Product Quality Assurance manager in a commercial entity or production environment.

    We are looking for an enthusiastic, fast learner and autonomous person ready to take on any challenges coming from a rapidly evolving regulatory environment and willing to develop his knowledge in EU and Suisse regulations related to pharmaceutical products (including vaccines), medical devices, food supplements and cosmetics.

    Requirements : Knowledge :

    Knowledge :

  • Chemical and pharmaceutical products
  • Pharmaceutical environment
  • International regulations, Good Manufacturing Practice (e.g EU GMP / GDP)
  • Writing abilities
  • English
  • Computer Applications
  • Organisation
  • Analysis / Synthesis
  • Team Spirit
  • Workload management
  • Data bases
  • French or German
  • Skills :
  • Planning
  • Planning
  • Customer orientation
  • At Sanofi diversity and inclusion are foundational to how we operate and are embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences.

    We recognize that to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.

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