Global Supplier Quality Specialist (w/m/d)
Basel, Switzerland
Job Description
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English
Global Supplier Quality Specialist (w/m/d)
Overview
For a project (remote work possible within Switzerland) at our client\\\'s site, a pharmaceutical company based in Basel, we are looking for an experienced
Global Supplier Quality Specialist (w/m/d)
8896
Contract
until 31.12.2022
Basel / Remote
Applications close 22 Nov 2023
Posted 16 Nov 2023
In this role, you are responsible for leading global supplier quality efforts, overseeing a substantial QAA remediation project, and managing the complete lifecycle of supplier qualification processes to uphold the highest standards in patient safety and drug quality.
Qualifications
English
Global Supplier Quality Specialist (w/m/d)
Overview
For a project (remote work possible within Switzerland) at our client\\\'s site, a pharmaceutical company based in Basel, we are looking for an experienced
Global Supplier Quality Specialist (w/m/d)
8896
Contract
until 31.12.2022
Basel / Remote
Applications close 22 Nov 2023
Posted 16 Nov 2023
In this role, you are responsible for leading global supplier quality efforts, overseeing a substantial QAA remediation project, and managing the complete lifecycle of supplier qualification processes to uphold the highest standards in patient safety and drug quality.
Qualifications
- Proven experience in global supplier quality, including the implementation of quality standards and guidelines with a bachelor\\\'s degree
- Extensive knowledge in cGMPs and cGDP requirements, ISO standards for supplier qualification, and QAA establishment process
- Proficient in Supplier Qualification and Supplier Monitoring
- Strong negotiation skills with the ability to take risks based on decisions
- Fluent in English
- Supplier Lifecycle management for project global QAA remediation to manage end-to-end QAA establishment process from authoring to signatures and appropriate system upload
- Independently responsible for managing the authoring/revision of QAA and Supplier Commitment Letters (SCLs) in due time as well as the route for review before initiating the approval process
- Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, and cGMP regulations
- Manage assigned systems and tools in an optimized way to facilitate lean global activities of QAA\\\'s
- Ensure with peers and supervisor, that the assigned project is embedded into the overall concept for the QA Ops-owned processes
- Collaborate closely with management and the team to report on progress for tight timelines of the QAA remediation project
- Ensure that the process is aligned with systems used by other stakeholders (exchange of data/information, lean process, elimination of redundancies)
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Job Detail
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Job IdJD1629170
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IndustryNot mentioned
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Total Positions1
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Job Type:Full Time
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Salary:Not mentioned
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Employment StatusPermanent
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Job LocationBasel, Switzerland
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EducationNot mentioned