MSAT Upstream Associate Director (Nantong, JS, CN, 226000)
About this opportunity
南通，中国 | 全职 | Job ID: 11621
Position Summary:
1. Leading upstream technology transfer and scale-up related work
领导上游技术转移和放大等相关工作
2. Support manufacturing related activities, leading upstream process-related deviation investigations and change controls
支持生产相关活动， 负责上游工艺相关偏差调查和变更
Your main responsibilities are:
1. Familiar with upstream related facilities, process flow, equipment operation, material management, tech transfer and PPQ (Process Performance Qualification).
熟悉上游厂房设施、工艺流程、设备操作、物料管理、技术转移及PPQ（工艺性能确认）所需知识要点。
2. Support daily manufacturing management, including deviation investigations, Corrective and Preventive Actions (CAPA), change control, and approval of technical plans/reports.
支持日常生产管理，包括偏差调查、纠正预防措施（CAPA）、变更控制及技术方案/报告审批。
3. Collaborate closely with all relevant departments to ensure projects progress as planned.
与所有相关部门紧密合作，确保项目按计划推进。
4. During PPQ stage, serve as the process owner and drive continuous process optimization and validation work.
PPQ阶段担任工艺负责人，推动持续工艺优化与验证工作。
5. Conduct MSAT upstream talent development and training work.
推进MSAT上游人才培养工作。
6. Support cross-border tech transfer to different CDMOs or production sites.
支持向不同CDMO或生产基地的跨国技术转移。
What you have to offer:
Chemical engineering, bioengineering, biology, pharmacy and other life sciences or engineering related majors.
化学工程， 生物工程， 生物学， 药学等生命科学或工程相关专业
Have over 8 years of antibody and recombinant protein upstream process development, MSAT or manufacturing work experience with a Ph.D degree or more than 12 years with a master’s degree
具有博士毕业8年以上或硕士毕业12年以上抗体和重组蛋白上游工艺开发， MSAT或生产相关工作经验
Excellent communication and coordination capability to work with internal and external teams independently
具备较强的沟通协调能力， 能够独立与内外部团队协作
Good written and verbal English proficiency
具有良好的英文水平
Adapt to diverse workflows, management styles and operational systems. 适应不同工作方式
BioNTech 重视每一位团队成员的福祉，为多元化的员工提供全面的福利保障。我们提供具有市场竞争力的薪酬方案，具体将根据职位、工作地点及候选人资历与经验综合确定。注：各项福利的实际适用范围、享有条件及具体内容可能因所在地而异，最终以公司内部政策及当地法律法规为准。
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提交申请即视为您知悉，招聘流程中将依相关法律法规进行背景调查。如您进入候选名单，BioNTech 将通过合作服务机构“HireRight”开展背景调查工作，招聘专员将及时与您沟通具体安排。
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Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 930 comparable Associate Director Manufacturing & CMC roles across 109 biopharma companies.
Salary context
271 of 930 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 930 comparable roles
+ 35 more countries
Seniority mix
930 of 930 peers have a known seniority level
Therapeutic area mix
12 of 930 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.