職位描述
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Implement GMP compliance with global GMP standards and China GMP requirement
根據總部和中國GMP要求,執行GMP符合性工作
● Ensure that QC specifications and analytical methods comply with applicable pharmacopeias requirements
確保QC的質量標準和分析方法符合相關藥典要求
● Ensure that CMC regulatory submissions are aligned with QC specifications and analytical methods.
確保QC的質量標準和分析方法和CMC注冊文件一致。
● Support Chinese Pharmacopeia commenting and implementation across the network
支持中國藥典在集團內的意見反饋與執行
● Maintenance of Master Method Validation Plan and the timely execution of method validation protocols and reports
維護驗證主計劃,及時執行方法驗證計劃和報告。
● Excute analytical transfers and local analytical method verifications.
執行分析方法轉移和本地分析方法確認。
● Provide technical guidance on test methods and relevant procedures.
對測試方法和檢測過程提供技術支持。
● Provide QC technical support and oversight to CMO activities
對CMO活動提供QC技術支持和監督
● Support regulatory inspections and partner audits
支持官方審計和合作伙伴審計
● Sample receipt, storage, distribution and disposal procedure management.
樣品的接收、存儲、分發及處理流程的管理。
● Reference and retention sample management.
參考留樣及常規留樣的管理。
● Packaging material standard sample management.
包材的標準樣管理。
● Reference standards management
標準品管理
● Third party QC labs management
第三方實驗室管理。
● Ensure support on manufacturing operations through troubleshooting and other product lifecycle testing.
確保支持生產過程中的故障排除和其他的產品生命周期測試。
● Manage the trending process in labs according to Roche PQS requirements and regulations
根據羅氏PQS和法規要求,管理實驗室的趨勢分析流程
● Stability program - chamber management, coordination with global and laboratories for timely execution of stability protocols and stability report, stability trending
穩定性安排-箱子管理、協調總部和實驗室以保證穩定性方案、報告以及穩定性趨勢分析的及時執行
● QC metrics generation and report, managing performance of quality system processes (TCM, Discrepancies, CAPA, etc) for QC
QC量度的生成及報告,管理QC相關的質量體系(變更、偏差、CAPA等)的指標
Qualifications and Experience
● Bachelor's Degree and above (Pharmacy, Master's Degree is preferred)
本科及以上學歷(藥學,碩士以上學歷優先考慮)
● More than 3 years pharmaceutical or related company
三年以上醫藥及相關領域工作經驗
● Excellent verbal and written English skill
出色的英語口語及書面能力
● Excellent project leading experience
出色的項目管理經驗
根據總部和中國GMP要求,執行GMP符合性工作
● Ensure that QC specifications and analytical methods comply with applicable pharmacopeias requirements
確保QC的質量標準和分析方法符合相關藥典要求
● Ensure that CMC regulatory submissions are aligned with QC specifications and analytical methods.
確保QC的質量標準和分析方法和CMC注冊文件一致。
● Support Chinese Pharmacopeia commenting and implementation across the network
支持中國藥典在集團內的意見反饋與執行
● Maintenance of Master Method Validation Plan and the timely execution of method validation protocols and reports
維護驗證主計劃,及時執行方法驗證計劃和報告。
● Excute analytical transfers and local analytical method verifications.
執行分析方法轉移和本地分析方法確認。
● Provide technical guidance on test methods and relevant procedures.
對測試方法和檢測過程提供技術支持。
● Provide QC technical support and oversight to CMO activities
對CMO活動提供QC技術支持和監督
● Support regulatory inspections and partner audits
支持官方審計和合作伙伴審計
● Sample receipt, storage, distribution and disposal procedure management.
樣品的接收、存儲、分發及處理流程的管理。
● Reference and retention sample management.
參考留樣及常規留樣的管理。
● Packaging material standard sample management.
包材的標準樣管理。
● Reference standards management
標準品管理
● Third party QC labs management
第三方實驗室管理。
● Ensure support on manufacturing operations through troubleshooting and other product lifecycle testing.
確保支持生產過程中的故障排除和其他的產品生命周期測試。
● Manage the trending process in labs according to Roche PQS requirements and regulations
根據羅氏PQS和法規要求,管理實驗室的趨勢分析流程
● Stability program - chamber management, coordination with global and laboratories for timely execution of stability protocols and stability report, stability trending
穩定性安排-箱子管理、協調總部和實驗室以保證穩定性方案、報告以及穩定性趨勢分析的及時執行
● QC metrics generation and report, managing performance of quality system processes (TCM, Discrepancies, CAPA, etc) for QC
QC量度的生成及報告,管理QC相關的質量體系(變更、偏差、CAPA等)的指標
Qualifications and Experience
● Bachelor's Degree and above (Pharmacy, Master's Degree is preferred)
本科及以上學歷(藥學,碩士以上學歷優先考慮)
● More than 3 years pharmaceutical or related company
三年以上醫藥及相關領域工作經驗
● Excellent verbal and written English skill
出色的英語口語及書面能力
● Excellent project leading experience
出色的項目管理經驗
工作地點
地址:上海浦東新區龍東大道1100號
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職位發布者
Whit..HR
上海羅氏制藥有限公司
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制藥·生物工程
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1000人以上
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中外合資(合資·合作)
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浦東新區龍東大道1100號
應屆畢業生
學歷不限
2025-12-30 11:36:16
1214人關注
注:聯系我時,請說是在江蘇人才網上看到的。
