Contract Duration: 1 year
Responsibilities:
* Execution of all daily QMS activities such as but not limited to: Write, review and approve SOPs as required, implementation, execution and administration of change controls, deviations and CAPAs.
* Support Trading Entity Compliance group to ensure related GxP activities which support global trading of products are compliant and efficient.
* Ensure that a quality management system is implemented and maintained, focusing on the management of authorized activities and the accuracy and quality of records, ensuring that relevant customer complaints are dealt with effectively.
* Ensure 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.
Requirements:
* Scientific Degree
* German language is mandatory
* Excellent knowledge of Swiss healthcare legislation, GxP regulations and industry standards.
* 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 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 & manage documentation.
* Ability to make decisions on GxP/pharmaceutical activities to ensure regulatory compliance of trading licenses and local regulatory requirements.
* Strong partnerships and collaborations to ensure clear definition of requirements and compliance to the respective trading licenses.
* A strong understanding of industry and business, applicable legislation and regulatory compliance requirements.
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