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  • 药物化学(副)主任
    工作地点:上海

    岗位职责:

    1、 领导并管理三个包括Ph.D.及硕士毕业生在内的20-30人新药研发团队;

    2、 制定项目执行计划,确保执行部门的资源分配和合理性,负责按照项目要求管理、监督研发人员,并指导下属人员开展工作;

    3、 严格控制监督项目的进展;

    4、 主持或参与新的药物靶标调研和新项目的立项申请;

    5、 负责项目组与用户的沟通与协调,以及项目组与公司内部资源的分配与优化;

    6、 领导多名项目经理的工作,并且协助药化负责人(副总裁)管理部门的工作。



    岗位要求:

    1、有机化学、药物化学等相关专业博士学历,具有8年以上与药物开发有关的工作经验,有海外学习或工作背景者优先;

    2、丰富的药物设计工作经验,熟练掌握有机合成、产物分离与结构鉴定等相关技能;

    3、较强的领导和管理能力,善长与不同层次科研及管理人员沟通。


    现在申请
  • 制剂研究经理/副主任
    工作地点:上海

    岗位职责:

    1、负责制剂部的管理工作,包括人员和团建建设、在研项目管理、合规性管理和实验室管理等;

    2、负责创新药制剂处方前研究、处方筛选制剂工艺放大、技术转移、为生产提供处方和工艺规程,解决项目过程中出现的处方/工艺/放大等问题,推动项目顺利开展;

    3、熟悉NMPA和FDA的各项相关法规,按注册法规要求、ICH相关要求组织新药的研发工作,负责申报资料的整理、归纳、汇总、原始记录、CTD资料的撰写及审核;

    4、负责培养和建设专业的制剂研发团队,组织部门的培训和考核工作;

    5、负责组织和优化制剂部的各项规章制度,并监督执行;



    岗位要求:

    1、硕士及以上学历,药剂、药学、制药等相关专业,有七年及以上的制剂研发经验,5年以上的研发管理经验,有眼科制剂研发能力的优先;

    2、有较强的主动学习能力,理论知识基础扎实,对制剂研发,剂型改进、工艺放大、分析研发有一定经验和深厚的技术功底;

    3、熟悉药品研发注册的相关政策和法规、国家新药审评技术要求及审评动向,熟悉申报资料的撰写;

    4、具备良好的英语读写能力,能够熟练的查阅各种文献,翻译相关文献资料;

    5、对工作具有高度的责任心,能够承受较大工作压力,具有良好的沟通、协调能力和团队管理能力。


    现在申请
  • 制剂研究员
    工作地点:上海

    岗位职责:

    1、制剂部分的文献调研、处方工艺设计及研究、稳定性研究和相关放大等工作;
    2、负责小试研究到中试生产的转化,及工艺交接或动态生产的工作;
    3、及时解决对小试研究、中试生产中遇到的常见问题;
    4、相关专利药的制剂技术规避,并能够撰写发明专利;
    5、撰写注册申报资料;
    6、维护和管理制剂研发相关设备,保证设备正常使用;
    7、按时完成上级领导交办的其他工作任务。



    岗位要求:

    1、具有团队合作精神,喜欢从事研发工作,工作细致,有责任心;
    2、本科以上学历,三年以上工作经验,药物制剂等相关专业;
    3、从事过制剂处方研究,具备制剂生产、研发等相关工作经验者优先。


    现在申请
  • Biology Director
    工作地点:上海

    岗位职责:

     

    Responsibility
    1. Responsible for establishing and managing in vitro bioassays of drug discovery projects, including but not limited to literature research, assay method & plan proposal.

    2. Responsible for establishment of emerging new technical platforms.
    3. Responsible for managing CRO companies of biology related projects, including selecting high quality CRO, timely communication to ensure the expectation for collaboration are met.  
    4. Team management and training junior scientists.
     


     


    岗位要求:

     Requirements
    1.Ph.D in immunology, biochemistry, cell biology and related majors with >4 year experience on bioassays in industry, biotech or CROs;

    Capable of independent discovery research, and capable of leading a team.
    2.A good learner for new drug discovery field and emerging new techs.
    3.Intensive in vitro biochemical and cellular bioassay experience;
    4.Familiar with common bioassay methods like ELISA, TR-FRET, ALPHA, FP, FACS, In-cell western etc.
    5.Experience on ocular drug discovery will be a plus ; Experience on high-throughput screening is a plus;
    6.Fluent oral and written communications skills in English;
    7.Strong sense of responsibility. Good communication skills and team-oriented.


    现在申请
  • Clinical Operation Director
    工作地点:上海

    岗位职责:

    Serve as Sr. Clinical Project Manager for international projects Phase I, II, III, IV for Bio Pharmaceutical & Medical Device projects, according to ESTERN Medical Standard Operating Procedures, ICH Guidelines and GCP with total responsibility.

    Responsible for the successful conduct of assigned projects.

    Serve as Project Manager for assigned business development opportunities.

    Liaise with senior management in the Delivery and Service Centers to ensure adequate resources are available for assigned projects.

    Responsible for on time, on-budget provision of client deliverables for assigned projects.


    岗位要求:

    Education / Qualifications:

    Required:

    University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).

    Detailed knowledge of financial control procedures

    Thorough knowledge of project management processes.

    Thorough knowledge of time and cost estimate development.

    Thorough knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.

    Excellent English and also preferably knowledge of some mid level Spanish or Portuguese language with superb grammar skills both written and verbal.

    Broad knowledge of drug development process and client needs.

    Preferred:

    Masters or other advanced degree.

    Detailed knowledge of ESTERN Medical and the overall structure of the organization.

    Basic knowledge of ESTERN Medical sales and business development strategies and procedures.

    Thorough knowledge of ESTERN Medical S.O.P.s

     

    Experience Required:Minimum of seven (7) years relevant clinical research experience in a pharmaceutical / medical device company/CRO, including at least four (4) years of full project management responsibility.

    In lieu of the above requirement, candidates with > five (5) years supervisory experience in a heath care setting and > five (5) years clinical research expe

    现在申请
  • Medical Director
    工作地点:上海

    岗位职责:

    Reporting directly to the VP of Ophthalmology and based in Shanghai.
    Function as medical expert on one or more VivaVision clinical development programs.

    Job Responsibilities

    • Lead the development and implementation of a clinical research plan 

    • Provide medical and scientific expertise into clinical development and protocol planning activities

    • Serve as expert medical and scientific point of contact for regulatory and ethics committee interactions

    • Plan and participate in data analyses and creation of key study-related outputs such as clinical study reports and publications 

    • Lead the development and implementation of a clinical research plan

    • Identify and propose projects to senior management for approval

    • Assist VP of Ophthalmology Research in prioritizing and allocating resources

    • Leverage external research collaborators as needed

    • Investigate, create, and/or develop new methods and technologies for project advancement

    • Assist in securing intellectual property, including detailed descriptions for patent filing and/or proof of concept work, as appropriate


     


    岗位要求:

    Minimum Qualifications

    • PhD in a relevant scientific discipline with 5 years’ industry experience

    • Expert knowledge of scientific principles and concepts

    • Significant knowledge of ophthalmic disorders

    • Excellent oral and written communication skills

    • Ability to work in a team-oriented environment but also be a self-starter, internally motivated, with the ability to work independently to drive the research forward

    • Scientifically rigorous, highly organized, with significant attention to detail

    Preferred Qualifications

    • PhD + Post-doc & MD in a relevant scientific discipline and 5 years with industry experience

    • Knowledge of the pathophysiology and treatment of ophthalmic disorders and related

    • Prior success discovering and developing successful novel medicines

    • Proven track record of leading research programs and establishing strong collaborations

    • High energy level, focus, a passion and sense of urgency for developing important new medicines for devastating diseases

     

    现在申请