職位描述
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在羅氏,我們鼓勵每位同事展現(xiàn)真實的自己;我們欣賞獨特且出眾的品質(zhì)。羅氏的文化鼓勵積極的表達(dá)、開放的對話和真誠的連結(jié),在這里,你將因為做自己而被重視、接納和尊重,并得到個人的提升和職業(yè)的發(fā)展。所有的這一切,都是為了更好地預(yù)防、阻止和治愈疾病,并確保醫(yī)療資源的可及性和可持續(xù)性。歡迎加入羅氏,一個重視每種聲音的地方。
職位
General
· Performance of physical and chemical package material testing, excipients
testing, product stability, release and in-process control testing and
necessary trending analysis under Lean lab management.
· Performance of testing in accordance with cGMP regulations and
Roche/Genentech standards and China GMP requirement.
· Supporting manufacturing operations by timely completion of package
material testing and excipients testing.
· Continuous improvement of processes and technology, in collaboration with
ASAT, to drive right *** time and efficiencies
· Ensuring test methods are validated according to relevant cGMP and
pharmacopeias in collaboration with ASAT.
· Supporting investigations due to OOS, OOT, OOE and other production-related
issues.
Technical and Functional
Implement GMP compliance with global GMP standards and China GMP requirement
· Provide QC staff with technical guidance on test methods and relevant
procedures.
· Ensure timely generation and reporting of test results in support of
manufacturing operations.
· Ensure that data, documentation and laboratory processes are in a constant
state of regulatory compliance and inspection readiness.
· Ensure system, computer, change control and analytical data is reviewed,
evaluated and approved against established criteria.
· Ensure all laboratory operations including test execution, review and data
documentation follow cGMP procedures.
· Collaborate with Lab Support to ensure calibration and maintenance of
laboratory equipment and systems.
· Direct QC Staff in the timely resolution of issues, including
discrepancies, investigations and implementation of CAPAs.
· Escalate any potential quality issues revealed during QC testing or
processing of products, especially quality or regulatory issues with the
potential to affect product quality or regulatory compliance.
· Support regulatory inspections and partner audits.
· Provide QC technical support and oversight to CMO activities
· Approve protocols and reports (e.g. third-party QC labs, MSAT or QC
studies, etc.).
· Support testing requirement for counterfeit product and special requirement
Marketing
職位
General
· Performance of physical and chemical package material testing, excipients
testing, product stability, release and in-process control testing and
necessary trending analysis under Lean lab management.
· Performance of testing in accordance with cGMP regulations and
Roche/Genentech standards and China GMP requirement.
· Supporting manufacturing operations by timely completion of package
material testing and excipients testing.
· Continuous improvement of processes and technology, in collaboration with
ASAT, to drive right *** time and efficiencies
· Ensuring test methods are validated according to relevant cGMP and
pharmacopeias in collaboration with ASAT.
· Supporting investigations due to OOS, OOT, OOE and other production-related
issues.
Technical and Functional
Implement GMP compliance with global GMP standards and China GMP requirement
· Provide QC staff with technical guidance on test methods and relevant
procedures.
· Ensure timely generation and reporting of test results in support of
manufacturing operations.
· Ensure that data, documentation and laboratory processes are in a constant
state of regulatory compliance and inspection readiness.
· Ensure system, computer, change control and analytical data is reviewed,
evaluated and approved against established criteria.
· Ensure all laboratory operations including test execution, review and data
documentation follow cGMP procedures.
· Collaborate with Lab Support to ensure calibration and maintenance of
laboratory equipment and systems.
· Direct QC Staff in the timely resolution of issues, including
discrepancies, investigations and implementation of CAPAs.
· Escalate any potential quality issues revealed during QC testing or
processing of products, especially quality or regulatory issues with the
potential to affect product quality or regulatory compliance.
· Support regulatory inspections and partner audits.
· Provide QC technical support and oversight to CMO activities
· Approve protocols and reports (e.g. third-party QC labs, MSAT or QC
studies, etc.).
· Support testing requirement for counterfeit product and special requirement
Marketing
工作地點
地址:上海浦東新區(qū)上海市浦東新區(qū)龍東大道1100
??
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詳細(xì)位置,可以參考上方地址信息
求職提示:用人單位發(fā)布虛假招聘信息,或以任何名義向求職者收取財物(如體檢費、置裝費、押金、服裝費、培訓(xùn)費、身份證、畢業(yè)證等),均涉嫌違法,請求職者務(wù)必提高警惕。
職位發(fā)布者
唐靜如HR
上海羅氏制藥有限公司
-
制藥·生物工程
-
1000人以上
-
中外合資(合資·合作)
-
浦東新區(qū)龍東大道1100號
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10年以上
本科
2026-03-25 17:33:37
912人關(guān)注
注:聯(lián)系我時,請說是在江蘇人才網(wǎng)上看到的。
