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Project Management

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Onsite

Project Management

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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