
普通员工/个人贡献者
AI 估算 · 15k–25k
生物制药生产岗位,要求经验且外企,上海生活成本高,薪资有竞争力。
该职位负责慢病毒载体的上游生产操作,包括工艺转移、细胞库建立及GMP生产设施维护
Bachelor’s degree or above in pharmaceutical or biological sciences, or a related discipline. At least 2 years of hands-on GMP upstream production experience with viral vectors; familiar with GMP manufacturing workflows such as cleanroom gowning, material transfer, and room clearance procedures; strong awareness of aseptic operations.
Execute activities related to manufacturing process transfer. Perform upstream production operations for lentiviral vectors and prepare associated production records and documentation. Establishment of cell banks for viral vector packaging. Routine maintenance of GMP production facilities. Manage the procurement and inventory of production materials. Assisting the PD team with relevant process development work as needed. Other tasks assigned by supervisors according to project requirements.
Candidates with process development experience for lentiviral vectors are preferred. Familiarity with lentiviral vector packaging processes and fundamental principles, such as traditional cell factory methods; experience with fixed-bed bioreactor platforms is preferred. Practical experience in scaled-up upstream production of lentiviral vectors and bioreactor cultivation.
优点
缺点 / 挑战
顶尖药企慢病毒生产岗,技术前沿、意义强,但工作强度大、弹性差。
外企薪资福利较好,但未明确具体数字;稳定性高。
涉及前沿慢病毒载体技术,有工艺开发机会,但未明确晋升路径。
生产岗位通常需要现场办公,可能涉及加班或倒班,弹性不足。
参与基因治疗药物生产,直接贡献于患者健康,行业前景好。