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Compliance QA Associate

Lieu de travail Zurich
Secteurs Pharmaceutique & Life Sciences
Type d'emploi poste permanent
Un salaire Negotiable
Référence BBBH549389

Compliance Quality Assurance Associate

Experis IT Switzerland is currently on the search for an experienced Quality Assurance Associate to join one of their clients, a well-known company. For this temporary assignment based in Zurich, we are in search of an English-speaking candidate who is available in a short notice.

Location: Zurich, Switzerland

Start Date: ASAP in June

Duration: 5 months contract with a high chance of further contract extension

Key responsibilities:

  • Write, review and approve SOPs as required
  • Implementation, execution and administration of change controls, deviations and CAPAs
  • Ensure that accurare record, as required by the individual elements of the QMS, are kept and maintained in a secure manner
  • Support Trading Entity Compliance group to ensure related GxP activities which support global trading of products are compliant and efficient
  • Ensuring that a quality management system is implemented and maintained
  • Focusing on the management of authorized activities and the accuracy of and quality of records
  • Ensuring that relevant customer complaints are dealt with effectively; ensuring approval of suppliers and customers; support in ensuring that self-inspections are performed at appropriate regular intervals following a prearranged programme and necessary corrective measures are put in place ensuring that any additional requirements imposed on certain products by national law are adhered to.

Your profile:

  • Strong knowledge of global regulations relating to GDP, licensing, imports/exports and controlled drug / substance compliance. GDP, distribution, warehousing and transportation experience or proven equivalent experience
  • Ability to make decisions on GxP/pharmaceutical activities to ensure regulatory compliance of Takeda trading licenses and local regulatory requirements
  • Good Knowledge of Swiss healthcare legislation, GXP regulations and industry standards
  • Ability to work successfully in multi-functional and multi-cultural teams
  • Demonstrate unquestionable integrity and professionalism
  • Ability to collaborate and partner well at all levels, globally, regionally & cross-functionally.
    Highly punctual, systematic, highly organized, & concise in communication
    Strong attention to details, ability to review & managing documentation

Don't hesitate and send us your CV and testimonials today through the link in the advert.

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