上海凯莱英生物技术有限公司
Project Management
Skills
RBusiness Development
2 months ago
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Important information
Contract type:
Permanent
Location:
Tianjin, China
Work mode:
Onsite
Published on:
12 August 2026
What they need
该职位来源于猎聘 Job Description
- Lead all project initiation and planning efforts. Participate in the implementation and execution of a given project. Establishes project objectives, timelines and deliverables. Defines project tasks and resource requirements. Closely monitor/control project progression to ensure project is completed on schedule and within budget. Reports project progress to all key stakeholders.
- Supports the technical team to investigate any project challenges by necessary risk assessment tools & techniques, then implements corrective measures.
- Serves as liaison with client contacts, manages day-to-day communications and organizes project team meetings.
- Represents company in project meetings, prepares meeting agenda and minutes, and follows up on action items.
- Evaluates and assesses project results and provides recommendations for future improvements.
- Provides support to the business development team joining customer visits, conferences or tradeshows.
- Facilitates the generation of Quotations/Proposals/Change Orders with inputs from key stakeholders for existing relationships. Qualifications for the position: Technical Skills / Knowledge:
- Candidate should possess strong and effective project management, problem solving and interpersonal skills and have a proven track record working cross-functionally across a wide variety of technical, business and operational areas.
- Demonstrates good understanding of the pharmaceutical industry and drug development.
- Minimum of 5 years of relevant pharmaceutical or biotech industry experience in discovery chemistry, CMC process development and/or GMP manufacturing.
- Working knowledge and understanding of regulatory standards (ICH, FDA) and industry trends in small molecule drug development is a plus.
- Experience in a Contract Research Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred, but not required.
- Must have working knowledge of MS Office products. Independence/Accountability:
- Must be a self-starter, self-motivated, and highly flexible.
- Must be organized and detailed-oriented. Problem Solving:
- Proven experience in creating and carrying out successful plans and processes to solve complex problems. Leadership Activities:
- Work closely with team members across all CDMO related business units and with the management team to ensure coordination of all efforts and real-time communication with all stakeholders.
- Communication Skills:
- Proficiency in both English and Mandarin is required.
- Excellent communications skills (verbal, written, and presentation skills). Customary Education and Experience:
- Masters (MS) or PhD in life sciences; chemistry preferred
- A minimum of 5 years pharmaceutical or CRO/CMO industry experience preferably in API process R&D and manufacturing and/or Drug Product R&D and manufacturing.
- Prior experience in project management or managing external research collaborations, with PMP certification is a plus.
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