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Implement GMP compliance with global GMP standards and China GMP requirement
根據(jù)總部和中國GMP要求，執(zhí)行GMP符合性工作
● Ensure that QC specifications and analytical methods comply with applicable pharmacopeias requirements
確保QC的質(zhì)量標(biāo)準(zhǔn)和分析方法符合相關(guān)藥典要求
● Ensure that CMC regulatory submissions are aligned with QC specifications and analytical methods.
確保QC的質(zhì)量標(biāo)準(zhǔn)和分析方法和CMC注冊(cè)文件一致。
● Support Chinese Pharmacopeia commenting and implementation across the network
支持中國藥典在集團(tuán)內(nèi)的意見反饋與執(zhí)行
● Maintenance of Master Method Validation Plan and the timely execution of method validation protocols and reports
維護(hù)驗(yàn)證主計(jì)劃，及時(shí)執(zhí)行方法驗(yàn)證計(jì)劃和報(bào)告。
● Excute analytical transfers and local analytical method verifications.
執(zhí)行分析方法轉(zhuǎn)移和本地分析方法確認(rèn)。
● Provide technical guidance on test methods and relevant procedures.
對(duì)測(cè)試方法和檢測(cè)過程提供技術(shù)支持。
● Provide QC technical support and oversight to CMO activities
對(duì)CMO活動(dòng)提供QC技術(shù)支持和監(jiān)督
● Support regulatory inspections and partner audits
支持官方審計(jì)和合作伙伴審計(jì)
● Sample receipt, storage, distribution and disposal procedure management.
樣品的接收、存儲(chǔ)、分發(fā)及處理流程的管理。
● Reference and retention sample management.
參考留樣及常規(guī)留樣的管理。
● Packaging material standard sample management.
包材的標(biāo)準(zhǔn)樣管理。
● Reference standards management
標(biāo)準(zhǔn)品管理
● Third party QC labs management
第三方實(shí)驗(yàn)室管理。
● Ensure support on manufacturing operations through troubleshooting and other product lifecycle testing.
確保支持生產(chǎn)過程中的故障排除和其他的產(chǎn)品生命周期測(cè)試。
● Manage the trending process in labs according to Roche PQS requirements and regulations
根據(jù)羅氏PQS和法規(guī)要求，管理實(shí)驗(yàn)室的趨勢(shì)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(wěn)定性安排-箱子管理、協(xié)調(diào)總部和實(shí)驗(yàn)室以保證穩(wěn)定性方案、報(bào)告以及穩(wěn)定性趨勢(shì)分析的及時(shí)執(zhí)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(bào)告，管理QC相關(guān)的質(zhì)量體系（變更、偏差、CAPA等）的指標(biāo)
Qualifications and Experience
● Bachelor's Degree and above (Pharmacy, Master's Degree is preferred)
本科及以上學(xué)歷（藥學(xué)，碩士以上學(xué)歷優(yōu)先考慮）
● More than 3 years pharmaceutical or related company
三年以上醫(yī)藥及相關(guān)領(lǐng)域工作經(jīng)驗(yàn)
● 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(xiàng)目管理經(jīng)驗(yàn)