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『保瑞-桃園廠』品保專員 QA Associate I/II

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Description

●Ensure change control system is robust and routed in a timely manner.
●Maintains an effective document control system.
●Develop, coordinate, monitor and track the personnel training programs.
●Ensure compliance with CSV master plan and procedures, relevant regulatory guidance, customer requirements for the implementation of computer system.
●Plan, execute and follow up on internal audit program.
● Coordinate, accompany and follow up Regulatory Authorities GMP inspection, PAI for new product and Third Party Audits by Customers.
● Perform supplier qualification and maintenance
●Manage the regulatory updates, implementation and compliance related procedures.
● Ensure Bora GDP procedures are established, followed and executed appropriately in compliance with Current Good Distribution Practices (cGDPs)
● Collect, monitor, and report the quality metrics for the oversight of quality system
Collect, compile, review annual product review document. Collect documents for customer annual report request(s).
●Lead, coordinate, support and execute QIP for site innovation, improvement and enhancement of regulatory requirements.
● Create and revise related SOPs and documents.
● Other tasks as assigned by the company.
● Handle and/or coordinate quality risk management of the site for risks evaluations, controls and mitigations.
● Support QA inspector daily activities as required

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請至保瑞藥業官方網站投遞個人履歷表,此職缺履歷登錄網址:
https://boracorpcdmo.wd108.myworkdayjobs.com/BoraExternalCareers/job/QA-Associate-II_9974

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