职位详情
职位描述
【上海招聘会】
以下参会单位均已参加“ 精英汇—第四届生物医药专场招聘会（上海）”，简历合适者可到场进行一对一的面谈。
招聘会链接： http://www.jobmd.cn/specials/sh2014
工作地点：新加坡
面试时间：04月19日（9:00-12:00）
联系方式：金先生 ******** ********
招聘职位1：Senior QA manager
Key Responsibilitie********
Manage, oversee, an******** the day-to-day activities in QualityAssurance for GMP product manufacture. Areas of responsibility will******** but are not limite********, Change Control, Document Control,Discrepancy Management an******** functions.
Provide leadership an******** to staff performing Quality oversightactivities.
Manage an******** all aspects of people processes relate******** theemployee life cycle.This includes the select******** hiring an********of personnel on company an******** pol******** systems an********.
Manage an******** the setting of goals for staff an******** regularlyschedule******** throughout the year. Ensure staff receives appropriateknowledge an******** development an******** opportunities.
招聘职位2：QA Manager (QAM12)
Job Description：
Lead, identify an******** strategic QA projects to implement pol********accomplish improvements an******** productivities in QA. Also workclosely with Operation Excellence team.
-Provide a safe, controlle******** environment in all areas ofresponsibility. Be aware of the site safety objectives an******** surethey are communicate******** understoo******** all staff.
-Responsibilities to instill new productivity tools an******** aninstrument of change in workflow, culture an******** set. This includesdeveloping training mater******** training an******** staff. Willnee******** stress an******** forwar******** tra******** educationan********.
招聘职位3：Senior / Quality Assurance (CT)
Job Description：
Be a member of the QA Operations team, with the following coreresponsibilitie********
- Full review of complete******** records to ensure compliance with cGMPper written procedures.
- Review an******** of SOPs, changes, ******** an********/preventativeactions.
- Review of GMP ******** e.g. manufacturing logbooks.
- Compile batch documentation for lot release within targetsdefine******** review an******** schedule.
- Ensure all associate******** are investigate******** close******** tolot release.
- Assess potential impact to product quality for open deviations duringlot release.
- Prepare responses for customer review observations.
更多招聘信息详见********
以下参会单位均已参加“ 精英汇—第四届生物医药专场招聘会（上海）”，简历合适者可到场进行一对一的面谈。
招聘会链接： http://www.jobmd.cn/specials/sh2014
工作地点：新加坡
面试时间：04月19日（9:00-12:00）
联系方式：金先生 ******** ********
招聘职位1：Senior QA manager
Key Responsibilitie********
Manage, oversee, an******** the day-to-day activities in QualityAssurance for GMP product manufacture. Areas of responsibility will******** but are not limite********, Change Control, Document Control,Discrepancy Management an******** functions.
Provide leadership an******** to staff performing Quality oversightactivities.
Manage an******** all aspects of people processes relate******** theemployee life cycle.This includes the select******** hiring an********of personnel on company an******** pol******** systems an********.
Manage an******** the setting of goals for staff an******** regularlyschedule******** throughout the year. Ensure staff receives appropriateknowledge an******** development an******** opportunities.
招聘职位2：QA Manager (QAM12)
Job Description：
Lead, identify an******** strategic QA projects to implement pol********accomplish improvements an******** productivities in QA. Also workclosely with Operation Excellence team.
-Provide a safe, controlle******** environment in all areas ofresponsibility. Be aware of the site safety objectives an******** surethey are communicate******** understoo******** all staff.
-Responsibilities to instill new productivity tools an******** aninstrument of change in workflow, culture an******** set. This includesdeveloping training mater******** training an******** staff. Willnee******** stress an******** forwar******** tra******** educationan********.
招聘职位3：Senior / Quality Assurance (CT)
Job Description：
Be a member of the QA Operations team, with the following coreresponsibilitie********
- Full review of complete******** records to ensure compliance with cGMPper written procedures.
- Review an******** of SOPs, changes, ******** an********/preventativeactions.
- Review of GMP ******** e.g. manufacturing logbooks.
- Compile batch documentation for lot release within targetsdefine******** review an******** schedule.
- Ensure all associate******** are investigate******** close******** tolot release.
- Assess potential impact to product quality for open deviations duringlot release.
- Prepare responses for customer review observations.
更多招聘信息详见********
职位要求
- 专业要求： 不限
- 最低学历： 本科
- 工作年限： 经验不限
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