岗位描述
教育程度/经验Education background/ Experience:
本科及以上学历,生物学,药学,化学或其他相关专业;Bachelor's degree or higher in Biology, Pharmacy, Chemistry, or a related field.
在生物技术或制药公司有质量控制、生产相关的合规管理经验;Experience in compliance management for quality control and manufacturing in biotech or pharmaceutical companies.
具备良好的GMP基础,对合规的原则有深入理解;熟悉NMPA,FDA,EU等GMP法规及指南;Solid understanding of Good Manufacturing Practice (GMP) fundamentals. In-depth knowledge of compliance principles. Familiarity with GMP regulations and guidelines (e.g., NMPA, FDA, EU).
英文可作为书面和口头交流工作语言; Proficient in English for both written and oral workplace communication;
有海外留学经验者,可适当放宽工作经验要求。Candidates with overseas study experience may be given more flexibility in the work-experience requirements.
其他要求(比如工作时间或特殊技能等)Other requirements (e.g.: working time, special skills)
具备良好的跨部门沟通和团队协作能力;Excellent cross-functional collaboration and teamwork skills.
具备良好的逻辑思维能力,主动学习、深入思考的能力;Strong logical thinking, proactive learning, and critical thinking skills.
能灵活调整时间,支持海外基地的工作。Ability to work flexible hours to support overseas operations (accommodating different time zones as needed.