Results 1 - 20 of 65
  • Zoetis Suzhou

    苏州市 终身制 Job title: Scientist Location: Suzhou Department: VMRD Position Summary To apply technical expertise and/or experiences to the design and execution of experiments/clinical trials in the development of veterinary vaccines. Show a high degree of independence in completing laboratory works/trials. Essential Duties and Responsibilities Contribute to the development of new and existing vaccines through membership in project teams, as appropriate to the role and required by the business. Activ...

  • Zoetis Suzhou

    苏州市 终身制 Summary To initiate, manage and/or direct activities aimed at the registration of new animal health products with a focus on vaccines and biopharma products. Essential Duties and Responsibilities Provide timely regulatory advice and guidance to project teams on the experimental designs for the registration of new veterinary products, this includes but not limited to study protocol/report review Prepare and review applications (field trial permit or product registration dossier) for regul...

  • Zoetis Suzhou

    苏州市 终身制 JOB DESCRIPTION Summarize the primary purpose & key accountabilities of the position, including scope of responsibility in 5-7 concise sentences. (i.e. Global vs. Country/Region) It may be helpful to complete this section after you have finished the other sections of the document. The clinical manager will provide strategic oversight of clinical programs and make key decisions on how clinical studies should be implemented to ensure high quality outcomes and animal welfare compliance....

  • Zoetis Suzhou

    Job Location: China Full/Part Time: Full-Time Regular/Temporary: Regular Responsibilities This position is based in Suzhou or Beijing and provides strategic and scientific leadership in Research and Development to the China R&D Teams, composed of scientists, clinicians, regulatory, project management, and administration groups. The objective is to leverage the Zoetis laboratories in China (with locations in Beijing and Suzhou) and the Global R&D network, as well as external expertise and...

  • Zoetis Beijing

    Job title: Senior Scientist Location: Beijing Department: VMRD Position Summary To apply advanced technical expertise/broad experiences in the design & execution of experiments/clinical trials for the development of veterinary vaccines. Position reports to the Director, VMRD Beijing Essential Duties and Responsibilities Apply advanced technical and functional knowledge to the design of experiments/clinical trials for the development of animal vaccines Lead project teams or sub-teams to devel...

  • Zoetis Shanghai

    POSITION SUMMARY The Regional Compliance Auditor will conduct on-site audits of Zoetis manufacturing sites, contractors and suppliers - with the goal of determining compliance gaps and necessary remediation plans. The auditor will promptly deliver/communicate audit findings using predetermined processes and methodology. The RCA will (as needed) assist with mock regulatory inspections as well as supporting agency inspections. Additonally - the auditor will gather, track, trend, and disseminate re...

  • Zoetis Suzhou

    苏州市 终身制 Job title: Scientist Location: Suzhou Department: VMRD Position Summary To apply technical expertise and/or experiences to the design and execution of experiments/clinical trials in the development of veterinary vaccines. Show a high degree of independence in completing laboratory works/trials. Essential Duties and Responsibilities Contribute to the development of new and existing vaccines through membership in project teams, as appropriate to the role and required by the business. Activ...

  • Zoetis Beijing

    北京市 终身制 Job Location: China Full/Part Time: Full-Time Regular/Temporary: Regular Responsibilities This position is based in Suzhou or Beijing and provides strategic and scientific leadership in Research and Development to the China R&D Teams, composed of scientists, clinicians, regulatory, project management, and administration groups. The objective is to leverage the Zoetis laboratories in China (with locations in Beijing and Suzhou) and the Global R&D network, as well as external exper...

  • Zoetis Suzhou

    苏州市 终身制 Job Location: China Full/Part Time: Full-Time Regular/Temporary: Regular Responsibilities This position is based in Suzhou or Beijing and provides strategic and scientific leadership in Research and Development to the China R&D Teams, composed of scientists, clinicians, regulatory, project management, and administration groups. The objective is to leverage the Zoetis laboratories in China (with locations in Beijing and Suzhou) and the Global R&D network, as well as external exper...

  • Zoetis Suzhou

    苏州市 终身制 职位简述: 生产经理应为苏州新疫苗制造工厂建立并领导生产部,包括:部门团队的招聘和发展、设备的确认、操作规程的制定以及GMP认证。生产经理也应与技术部同事紧密合作从新产品到生产的转化。当工厂开始运营,生产经理将负责确保持续供应高质量疫苗给我们的客户。 职位职责: 组织生产主管根据生产主计划制定详细的日生产计划,确保计划正确地实施。 为生产管理提供指导,保持并提高生产能力和效率以确保100%客户供应。 按照农业部GMP法规和硕腾质量体系运营,确保合格、有效和安全产品的生产。 完成新生产设备的验证和新工艺的验证。 制定并维护生产部的安全、健康和环境保护的理念和文化。 推进六西格玛工具的应用,确保行业竞争优势。 确保先进的工艺来提高抗原收率,降低污染可能性和报废。 支持技术部门解决工艺问题,完成新产品的技术转化。 发展员工的敬业精神和决策能力,持续为各岗位建立人才库。支持每个员工合理的个人发展计划。 制定部门预算,在批准的预算范围内控制生产支出。 招聘要求: 大学本科以上学历,微生物学、生物学、病毒学、制药工程或相关专业。 疫苗或相似生物制品制造公司8年以上工作经验,5年以上...

  • Zoetis Shanghai

    POSITION SUMMARY The Regional Compliance Auditor will conduct on-site audits of Zoetis manufacturing sites, contractors and suppliers - with the goal of determining compliance gaps and necessary remediation plans. The auditor will promptly deliver/communicate audit findings using predetermined processes and methodology. The RCA will (as needed) assist with mock regulatory inspections as well as supporting agency inspections. Additonally - the auditor will gather, track, trend, and disseminate re...

  • Zoetis Suzhou

    苏州市 终身制 JOB DESCRIPTION Summarize the primary purpose & key accountabilities of the position, including scope of responsibility in 5-7 concise sentences. (i.e. Global vs. Country/Region) It may be helpful to complete this section after you have finished the other sections of the document. The clinical manager will provide strategic oversight of clinical programs and make key decisions on how clinical studies should be implemented to ensure high quality outcomes and animal welfare compliance....

  • Zoetis Suzhou

    苏州市 终身制 JOB DESCRIPTION Summarize the primary purpose & key accountabilities of the position, including scope of responsibility in 5-7 concise sentences. (i.e. Global vs. Country/Region) It may be helpful to complete this section after you have finished the other sections of the document. The VMRD Pilot Lead will serve as a vaccine manufacturing Subject Matter Expert (SME) for GMS and VMRD. The incumbent will provide technical leadership and support for vaccine projects and for process/analy...

  • Zoetis Beijing

    Job title: Senior Scientist Location: Beijing Department: VMRD Position Summary To apply advanced technical expertise/broad experiences in the design & execution of experiments/clinical trials for the development of veterinary vaccines. Position reports to the Director, VMRD Beijing Essential Duties and Responsibilities Apply advanced technical and functional knowledge to the design of experiments/clinical trials for the development of animal vaccines Lead project teams or sub-teams to devel...

  • Zoetis Beijing

    Job Location: China Full/Part Time: Full-Time Regular/Temporary: Regular Responsibilities This position is based in Suzhou or Beijing and provides strategic and scientific leadership in Research and Development to the China R&D Teams, composed of scientists, clinicians, regulatory, project management, and administration groups. The objective is to leverage the Zoetis laboratories in China (with locations in Beijing and Suzhou) and the Global R&D network, as well as external expertise and...

  • Zoetis Shanghai

    POSITION SUMMARY SCOPE OF THE POSITION : Responsible for the quality management system (quality control and quality assurance) and regulatory compliance of third-party manufacturing sites producing Zoetis products and API suppliers sourcing for the company. POSITION RESPONSIBILITIES The External Supply Quality Assurance Manager is responsible for: Contractor Management : General: Ensure contractors have applicable quality systems and comply with GMP / regulatory requirements and Zoetis expectati...

  • Zoetis Shanghai

    上海市 终身制 POSITION SUMMARY SCOPE OF THE POSITION : Responsible for the quality management system (quality control and quality assurance) and regulatory compliance of third-party manufacturing sites producing Zoetis products and API suppliers sourcing for the company. POSITION RESPONSIBILITIES The External Supply Quality Assurance Manager is responsible for: Contractor Management : General: Ensure contractors have applicable quality systems and comply with GMP / regulatory requirements and Zoetis e...

  • Zoetis Suzhou

    JOB DESCRIPTION Summarize the primary purpose & key accountabilities of the position, including scope of responsibility in 5-7 concise sentences. (i.e. Global vs. Country/Region) It may be helpful to complete this section after you have finished the other sections of the document. The VMRD Pilot Lead will serve as a vaccine manufacturing Subject Matter Expert (SME) for GMS and VMRD. The incumbent will provide technical leadership and support for vaccine projects and for process/analytical te...

  • Zoetis Beijing

    Job Location: China Full/Part Time: Full-Time Regular/Temporary: Regular Responsibilities This position is based in Suzhou or Beijing and provides strategic and scientific leadership in Research and Development to the China R&D Teams, composed of scientists, clinicians, regulatory, project management, and administration groups. The objective is to leverage the Zoetis laboratories in China (with locations in Beijing and Suzhou) and the Global R&D network, as well as external expertise and...

  • Zoetis Suzhou

    苏州市 终身制 职位简述: 生产经理应为苏州新疫苗制造工厂建立并领导生产部,包括:部门团队的招聘和发展、设备的确认、操作规程的制定以及GMP认证。生产经理也应与技术部同事紧密合作从新产品到生产的转化。当工厂开始运营,生产经理将负责确保持续供应高质量疫苗给我们的客户。 职位职责: 组织生产主管根据生产主计划制定详细的日生产计划,确保计划正确地实施。 为生产管理提供指导,保持并提高生产能力和效率以确保100%客户供应。 按照农业部GMP法规和硕腾质量体系运营,确保合格、有效和安全产品的生产。 完成新生产设备的验证和新工艺的验证。 制定并维护生产部的安全、健康和环境保护的理念和文化。 推进六西格玛工具的应用,确保行业竞争优势。 确保先进的工艺来提高抗原收率,降低污染可能性和报废。 支持技术部门解决工艺问题,完成新产品的技术转化。 发展员工的敬业精神和决策能力,持续为各岗位建立人才库。支持每个员工合理的个人发展计划。 制定部门预算,在批准的预算范围内控制生产支出。 招聘要求: 大学本科以上学历,微生物学、生物学、病毒学、制药工程或相关专业。 疫苗或相似生物制品制造公司8年以上工作经验,5年以上...

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