Careers

This is an exciting opportunity to be a key contributor at ChemPartner, a leading Shanghai based Contract Research Organization specializing in drug discovery services. As more and more Pharma and Biotech companies look for alliance partners to increasingly provide intellectual contributions and exceptional technical expertise, ChemPartner is uniquely positioned to not only be a LifeScience […]

职位描述 负责完成常用剂型的创新药、仿制药处方工艺筛选及优化等制剂药学相关研究工作。 评估项目可行性，把握项目难点，制定处方工艺研发方案，执行项目计划书。 掌握项目进程，指导3-5名组内研发技术人员，撰写项目进度及开发报告，完成相关中、英文申报资料。 管理并维护相关仪器设备，保证实验室的正常运行与研发合规性。 与客户进行前瞻性的研发策略交流，根据项目实际进展情况，适时地对项目策略和计划进行必要调整，必要时起草补充协议或撰写审核新方案。 参与BD，对商业化活动提供必要的科学技术支持;参与或主导新客户访问接待或电话会议。 为小组招聘新员工，并对其进行培训和指导;参与员工的绩效管理，促进员工在组内的发展提升。 完成领导交办的其他任务。 任职要求: 本科及以上学历，药剂学及相关专业。 5-10年以上制剂研发经验，有团队管理经验优先。 药物制剂研发相关专业知识与技能，具备一定的制剂开发及生产放大经验: 熟悉国内外药品相关的法律法规、规范性文件和相应的工作程序，具有多个制剂项目的申报注册经验: 能够熟练阅读、书写专业英语。 理解ICH等研发技术指导原则，熟悉国内外注册申报与审评要求。 工作地点:中国上海，奉贤区

职位描述: 有丰富，扎实的有机合成经验，熟练掌握有机合成、产物分离与结构鉴定技能; 熟悉现代有机合成技术和药物化学专业知识，能设计多步复杂的有机合成反应;能设计并合成小分子药物; 熟练掌握文献检索手段，熟练阅读(包括英文)文献和书写英文; 熟练掌握各种常见有机化学专业软件/数据库和办公软件的应用; 熟练编写中文和英文工作报告; 负责研发团队合成项目整体管理工作，包括方案选择与制定，沟通实施，进程把控，项目评估等; 负责研发部门技术难点问题的指导处理; 按照公司安全及GMP质量控制规范，负责工艺优化，与相关部门紧密合作完成中试生产。 负责团队管理和团队建设; 任职要求: 有机合成、药物化学、制药工程等相关专业; 硕士以上学历，5-10年以上有机合成或药物化学研发工作经验; 具备较强的科研力，深刻理解有机合成专业，具备丰富的有机合成理论知识和合成经验 ; 具备优秀的团队管理能力， 较强的责任心，具有良好的职业素养和沟通管理能力，创 新意识和较强的团队合作精神; 工作地点:中国上海，奉贤

职位描述: 负责研发团队的日常管理和业务指导，保障研发团队高效运行。 领导研发团队根据项目要求，制定研发流程和工作计划执行并指导具体研究工作; 负责制定研发团队的目标计划和绩效考核体系，不断提高研发团队效率。 配合 BD 部门负责市场业务推广，保持与客户的紧密沟通。 职位要求: 有机合成、药物化学等相关专业，博士及以上学历; 15年以上知名医药公司或 CRO/CDMO 原料药技术研发和管理经验，深刻理解CDMO业务的特点和要求; 至少5年以上技术研发团队管理经验，具备系统的原料药研发及工艺技术开发相关经验; 具有多年原料药(创新药为主)工艺开发经验和良好的实绩。熟悉创新药工艺研发流程; 有良好的组织协调能力及沟通能力，英文可以作为工作语言，听说读写流利。 工作地点:中国上海，奉贤区

职位描述: 参与制定公司发展战略与年度经营计划，组织制定并实施生产规划; 全面负责组织优化工厂生产运营体系及各项制度流程; 随时掌握生产状态，协调各部门的沟通与合作，及时解决生产中出现的各类问题; 负责生产设备管理，负责原料药(创新药较多)生产工艺并推进新的工艺实施标准 保证生产一切安全措施的执行实施，实现零意外发生; 组织监督确保生产过程中各项工艺、质量、设备、成本、产量指标等。 任职要求: 大学本科以上学历，药学、化学或化工等相关专业; 至少15年以上行业经验，深刻理解CDMO业务的特点和生产管理要求 至少有10年以上原料药厂生产管理实践经验并且有丰富的GMP认证实战经验。 至少有管理50人及以上的团队经验，至少5年以上的中高层生产管理经验。 工作地点:中国上海，奉贤区

职位描述: 带领分析团队及时有效的完成所有项目任务，具体如下: 负责指导监督整个分析团队的日常工作包括分析方法开发、验证、稳定性等研究工作; 给予分析团队最科学的管理和指导，建立一支符合效率及合规性的分析团队; 指导和监督所有ARD负责项目的方法转移和各项协调; 审阅所有的ARD相关的技术文件，包括分析方法、报告、技术转移文件、SOP等; 提供产品注册所需的支持文件等; 协调内部分析和QA的要求确保公司CGMP政策的执行; 参加国内外客户的技术及讨论会议; 给予团队成员相应的技术、安全、GMP等方面的培训; 任职要求: 博士学位，药物分析，分析化学或相关专业;15年以上分析研发的相关工作经验，其中 至少10年以上直接管理过ARD或者QC团队，如经验丰富可适当降低学历; 熟练掌握HPLC、GC、LC-MS等分析仪器原理及色谱分析等 熟悉国内外的GMP法规政策 熟悉制药行业尤其CDMO的运作方式 具有良好的沟通及协调能力 优秀的英文听说读写能力 工作地点:中国上海，奉贤区

岗位描述 参与制订、修订、审核SOP，并审核SOP的分发、回收、销毁等文档工作; 负责与GLP实验室QAU部门相关的所有文件管理工作; 检查研究项目实验过程操作中的关键环节; 审核试验方案、试验记录和总结报告; 定期检查动物饲养设施、实验仪器设备、档案管理和供试品管理工作; 向SD、部门负责人和机构负责人书面报告检查发现的问题，并跟踪整改情况; 负责实施供应商审计，接待客户的审计工作; 对检查/审计结果进行阶段性分析，并对机构工作人员进行GLP规范性培训; 其他与GLP实验室质量体系相关的工作。 任职要求 本科以上学位，医药、生物、药理学、毒理学等专业 具有至少三年GLP毒理实验室QA工作经验(动物实验相关) 口语和书面表达能力较强 英文书写能力较强 地点:中国，江苏启东，滨海高新技术园区

Job Description As the Head of Biologics Manufacturing you will, provide direction and tactical leadership to the Biologics Manufacturing, including upstream, downstream, Formulation and fill finish. You will oversee, manage, and direct the initiatives and daily activities of the biologics manufacturing operations. You will collaborate with support departments to ensure manufacturing production goals are achieved […]

Key Responsibilities Be responsible for setting up and expanding biologics manufacturing capabilities, such as antibody, ADC and cell based therapeutics, from initial design to final run Be responsible for profitability of the site to meet corporate financial targets, including strategic planning, business development with the support from corporate BD team Be responsible for routine operation […]

The Associate Director/Director of Analytical Development & Protein Characterization Group is responsible for leading the group for carrying out analytical development activities, as well as protein/antibody characterization activities for biologics drug products. He / she is mainly responsible for leading the team to develop a variety of analytical methods for supporting testing of biologics drug […]

Main Responsibilities The Manager & Associate Director & Director of the protein analytical chemistry group has the responsibility of leading a group of analytical development scientists & quality control analysts for the development, improvement, and execution of a variety of biochemical and analytical methods for the analysis of proteins, antibodies, peptides, as well as chemicals, […]

The (Assistant /Associate) /Director of the bioassay group has the responsibility of leading a group of analytical development scientists & quality control analysts for the development, improvement, and execution of a variety of biochemical and cell based assays for demonstrating in vitro protein-target binding/functional activities, as well as cell based activities/functions, including cellular proliferation activity, […]

Responsibilities Lead multiple biologics CMC projects, and act as the head of project teams. Coordinate the activities and tasks of sub-project teams and clients, ensure projects to be completed according to the requirements and time line. Provide technical recommendations to the team and client if needed. Hold regular communication with clients in written and oral […]

Responsibilities Lead a team of scientists and associates to develop the processes of cell fermentation from small scale to production scale for therapeutic protein in laboratory, pilot and production setting. Develop and customize the cell culture for fermentation if needed. Design, execute and supervise fermentation development programs. Excellent troubleshooting skill is needed. Hold regular communication […]

Main responsibilities Lead a team of scientists and associates to screen and develop stable cell lines for therapeutic protein expression in the industrial setting. Design, execute and supervise cell screening and stable cell line development troubleshooting skill is needed. Hold regular communication with clients in written and oral formats. Write and review technical reports and […]

Responsibilities Lead or participate development projects of LC-MS/MS based bioanalytical methods in PK, PD, biomarker areas, and responsible for the quality of the developed method. Effectively communicate with vendors, coworkers and supervisors with method related issues and provide progress updates regularly if necessary. Independently design and perform small molecule bioanalysis method development with global validation […]

To be responsible for method development, validation and implementation of ligand based analysis of antibodies/ADC/biomarkers in support GLP clinical large molecule PK/ADA/Nab studies. Responsibilities Design, develop and validate the ligand based analysis method in various biological samples including tissues/plasma/serum under GLP regulations. Analyze large molecule samples from pre-clinical or clinical GLP studies using immuno-assays or […]

Job Description As a Director/Sr. Director you will be responsible for leading a group of scientists to support pre-clinical pharmacokinetics. Responsibilities To lead a group of scientists providing quality DMPK services including study design, in-life, bioanalytical, data analysis and report writing for the clients world wide To participate as DMPK representative in multiple integrate service […]

Job Description To propose safety and preclinical strategies, design and coordinate appropriate non-GLP and GLP Tox to support preclinical development of drug candidates successfully IND filing To implement tox studies in preparing protocols, monitoring study progress, analyzing data and writing reports and regulatory documentation and filing To coordinate cross-functional effort (Discovery, Pharmacology, PKPD, BioAnalytical, CMC […]

Job description You will be responsible for leading a bioanalytical group to support pre-clinical functional areas including DMPK, biology/pharmacology, and biologics. Primary Responsibilities Manage a team to design, develop, and validate various bioanalytical methods, majority of which are LC-MS based. Manage a team to analyze biological samples derived from pre-clinical or clinical studies; analytes range […]

Key Accountabilities To coordinate the entire process of pharmacokinetics (PK) studies from initiation of the study to the report writing for quality and timely delivery To communicate with clients about technical details, project update and timeline Scope of the Job To design PK/PKPD/Tox studies, write study proposals, protocols, in-life summaries and study reports To analyze, […]

Job Description Leading a group of scientist and be responsible for the humanization and optimization of antibody candidates generated by hybridoma- or phage display-technology. Managing the group and taking responsibility for its projects by driving and coordinating his/her direct reports in achieving the specific objectives of the respective research projects. Representing the Biologics department in […]

Job Description Leading a group of scientists and be responsible for recombinant protein production including construct design, expression and purification in E.coli, insect cell, or mammalian systems. Managing the group and taking responsibility for its projects by driving and coordinating his/her direct reports in achieving the specific objectives of protein generation projects. Taking responsibility for […]

Responsibilities Lead therapeutic antibody discovery programs including reviewing project targets, design study plan with clients and ChemParter project leaders, draft or edit project proposals and reports. Provide scientific advice and leadership to ChemPartner project teams and input to clients in driving the project to successfully achieve specific objectives and milestones. Act in a project management […]

The candidate will lead a group of scientists working on in vitro assays supporting drug discovery projects. Lead assay development on both biochemical and cell-based assays, compound screening, and other in vitro experiments. Communicate with clients, generate study proposals, and analyze data. Manage a group of scientists and the associated laboratory and equipment. Work with […]

Responsibilities Maintain and improve performance of team and lab resources consistently with operational budget limitations. Advocate for best choice of capital and consumable resources to ensure effective function and state-of-the-art analytical chemistry support to the extent possible. Work together with department head to develop and implement organizational and scientific objectives in close coordination with members […]

Responsibilities This position will require the candidate to possess and leverage deep knowledge and capabilities to deliver pre-clinical or clinical candidates. The senior chemist will partner with key scientists in the field of oncology and immunology etc., represent medicinal chemistry on cross-functional project teams, and be co-responsible for building, managing, and delivering projects to meet […]

Responsibilities Leads multiple teams to support drug discovery efforts across multiple therapeutic areas and target types. Communicates with clients on a regular basis to present data, discuss results and provide input on project direction as needed. Interacts with different functions such as Computational Chemistry; DMPK, and Biology showing a deep understanding of all areas of […]