毒理(副)总监 | Toxicology (Associate) Director
工作地点 | Work Location
北京(提供完善的通勤配套与办公环境,基地为集团重点打造的研发创新中心,配备国际一流的实验设备与安全评价设施)
Beijing (Well-equipped with commuting support and office environment; Base is a key R&D and innovation center of the group, equipped with world-class experimental equipment and safety evaluation facilities)
职位概要 | Job Overview
作为核心技术管理岗位,您将主导毒理平台的从 0 到 1 搭建与迭代优化,构建符合国际标准的非临床安全评价体系。带领跨职能团队(涵盖毒理学研究、动物实验、数据分析等专业方向),全程负责临床前试验的方案设计、流程管控、实验实施与结果深度分析,确保所有试验严格遵循 GLP 规范及国际国内法规要求,保障实验数据的真实性、可靠性与实验报告的科学严谨性。同时,您将深度参与公司创新药 / 医疗器械研发管线的安全评估决策,为项目推进提供关键毒理学技术支撑,推动研发成果高效转化。
As a core technical management role, you will lead the construction and iterative optimization of the Toxicology Platform from scratch, establishing a non-clinical safety evaluation system that meets international standards. You will lead a cross-functional team (covering toxicology research, animal experiments, data analysis and other professional fields) to take full responsibility for the design, process control, implementation and in-depth result analysis of preclinical trials. You will ensure all trials strictly comply with GLP standards and international/domestic regulatory requirements, and guarantee the authenticity, reliability of experimental data and the scientific rigor of experimental reports. Meanwhile, you will deeply participate in the safety assessment and decision-making of the company's innovative drug/medical device R&D pipeline, provide key toxicological technical support for project advancement, and promote the efficient transformation of R&D achievements.
我们期待这样的您 | We Expect You to Have
- 学历与专业背景 | Education & Professional Background
:拥有毒理学、药理学、动物医学或相关领域的硕士及以上学历,博士学历优先,具备扎实的理论基础与前沿的行业认知。
Master's degree or above in Toxicology, Pharmacology, Veterinary Medicine or related fields; PhD degree is preferred. Solid theoretical foundation and cutting-edge industry awareness are required.
- 专业经验 | Professional Experience
:具备 8 年以上非临床安全评价相关工作经验,其中至少 3 年团队管理经验;熟悉药物 / 医疗器械从早期研发到上市申报各阶段的毒理研究需求,有成功搭建或优化毒理平台、主导关键试验项目的经验者优先。
More than 8 years of work experience in non-clinical safety evaluation, with at least 3 years of team management experience; Familiar with the toxicological research needs of drugs/medical devices at all stages from early R&D to marketing application; Experience in successfully building or optimizing toxicology platforms and leading key trial projects is preferred.
- 法规与技术能力 | Regulatory & Technical Capabilities
:精通 FDA、NMPA、EMA 等国内外药品 / 医疗器械监管机构的相关法规、指导原则及 GLP 规范,能够独立完成符合国际标准的毒理试验方案设计与报告撰写;具备较强的问题解决能力,能针对试验过程中的复杂技术问题提出有效解决方案。
Proficient in relevant regulations, guidelines and GLP standards of domestic and foreign drug/medical device regulatory authorities such as FDA, NMPA and EMA; Capable of independently completing the design of toxicology test protocols and writing reports that meet international standards; Strong problem-solving ability, able to propose effective solutions to complex technical problems during the trial process.
- 管理与协作能力 | Management & Collaboration Abilities
:具备出色的团队领导与协调管理能力,能够激发团队潜力,推动跨部门(如研发、质量、注册等)高效协作;拥有良好的中英文沟通与表达能力,可顺畅对接国际合作项目与海外团队。
Excellent team leadership and coordination management skills, able to stimulate team potential and promote efficient collaboration across departments (such as R&D, Quality, Registration, etc.); Good Chinese and English communication and expression skills, able to smoothly connect with international cooperation projects and overseas teams.
我们为您提供 | We Provide You With
- 行业内极具竞争力的薪酬福利体系,包括基本工资、绩效奖金、年终分红、长期激励计划等;
- A highly competitive salary and welfare system in the industry, including basic salary, performance bonus, year-end bonus, long-term incentive plan, etc.;
- 完善的职业发展通道,支持横向轮岗与纵向晋升,为您提供成为行业顶尖毒理专家的成长平台;
- A sound career development path, supporting horizontal rotation and vertical promotion, providing you with a growth platform to become a top toxicology expert in the industry;
- 与国内外顶尖科研团队、行业专家交流合作的机会,参与前沿研发项目,拓展国际视野;
- Opportunities to communicate and cooperate with top domestic and foreign scientific research teams and industry experts, participate in cutting-edge R&D projects, and expand international horizons;
- 舒适的办公环境、健全的保障福利(五险一金、补充商业保险、年度体检、带薪年假等)及人性化的员工关怀体系。
- Comfortable office environment, sound security benefits (five social insurances and one housing fund, supplementary commercial insurance, annual physical examination, paid annual leave, etc.) and humanized employee care system.
加入我们 | Join Us
如果您渴望在创新医疗领域施展才华,推动中国乃至全球的医药健康事业发展,我们诚挚邀请您加入请将您的中英文简历发送至:
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(邮件主题请注明 "毒理(副)总监 - 姓名 - 来源领英"),我们将在 3 个工作日内与符合要求的候选人取得联系。
If you are eager to display your talents in the innovative medical field and promote the development of China's and even the world's medical and health industry, we sincerely invite you to join us Please send your Chinese and English resumes to:
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(please note the email subject as "Toxicology (Associate) Director - Name - Source LinkedIn"), and we will contact qualified candidates within 3 working days.