QA Compliance Specialist
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Update day: 29-03-2024
Category: Administrative / Clerical / Assistant Sales Consulting / Customer Service Legal / Contracts Executive management
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Job content
- Salary:60 - 66 CHF gross per hour
- REF Number:00056282
- Consultant:Adrien Guimard
- Contact:0041 (0) 800 106 106
- Date Published:08.11.2023
- Sector:
- Location:Opfikon,
- Discipline:
QLS are recruiting for a Quality Compliance Specialist to join a Global Pharmaceutical company based in Zurich on a 4-5 months contract.
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
- Ensure that accurare record, as required by the individual elements of the QMS, are kept and maintained in a secure manner
- Support Trading EntityCompliance group to ensure related GxP activities which support Takeda’s global trading of products are compliant and efficient
Activities include:
Ensuring that a quality management system is implemented and maintained focusing on themanagement 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 qualification:
- Scientific Degree
- 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 & managing documentation
- Ability to make decisions on GxP/pharmaceutical activities to ensure regulatory compliance of Takeda trading licenses and local regulatory requirements
- Key interactions with global and regional stakeholders including SupplyChain, Legal, Tax, BU’s, Quality. Strong partnerships and collaborations to ensure clear definition of requirements and compliance to the respective trading licenses.
- Key interactions with numerous stakeholders in Quality (TE RP, OpU quality, Plant and Regional Quality, External Supply Quality)
- A strong understanding of industry and business, applicable legislation and regulatory compliance requirements.
- Multiple countries and business units, complex mix of supply & distribution models, multiple regulatory frameworks and a wide diversity of products
Apply:
For more information or to apply for this position, please contact Adrien on 0041 (0) 800 106 106 or email aguimard@ckqls.ch. Please could you send any correspondence in English. Please quote job reference 56282 in all correspondence.
Adrien Guimard
Senior Recruitment Consultant
T: +41 (0) 800 106106
Deadline: 13-05-2024
Click to apply for free candidate
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