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Senior Manager/Associate Director, CMC Project Management, Liverpool
Location: Liverpool, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Views: 7
Posted: 16.06.2025
Expiry Date: 31.07.2025
Job Description:
Overview
The Senior Manager/Associate Director Project Manager will be responsible for managing projects within STA, WuXi’s API and Drug Product development and manufacturing division. Leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team, and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting STA’s services in conferences/trade shows.
Please note this is a remote (work from home) position within the UK.
Responsibilities
* Lead all project initiation and planning efforts. Participate in the implementation and execution of a given project.
* Establish project objectives, timelines, and deliverables. Define project tasks and resource requirements.
* Closely monitor/control project progression to ensure project is completed on schedule and within budget. Report project progress to all key stakeholders.
* Support the technical team to investigate any project challenges by necessary risk assessment tools & techniques, then implement corrective measures.
* Serve as liaison with client contacts, manage day-to-day communications, and organize project team meetings.
* Represent the company in project meetings, prepare meeting agenda and minutes, and follow up on action items.
* Evaluate and assess project results and provide recommendations for future improvements.
* Support the business development team by joining customer visits, conferences, or tradeshows.
* Prepare Quotations/Proposals/Change Orders with inputs from key stakeholders for existing relationships.
Qualifications
Education and Experience:
* Master's (MS) or PhD in life sciences; chemistry preferred
* A minimum of 10 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 desired.
* Strong and effective project management, problem-solving, and interpersonal skills with a proven track record working cross-functionally across technical, business, and operational areas.
* Good understanding of the pharmaceutical industry and small molecule drug development.
* Minimum of 5 years of relevant pharmaceutical or biotech industry experience in CMC process development and/or GMP manufacturing.
* Knowledge of current regulations and industry trends for small molecules, manufacturing, and testing. Oligonucleotide and Solid State Peptide experience is a plus.
* Experience in CRO or CMO is preferred but not required.
* Proficiency with MS Office, especially MS Project.
Additional Skills and Qualities
* Self-starter, self-motivated, highly flexible, organized, and detail-oriented.
* Proven problem-solving skills with successful planning and process implementation.
* Ability to work closely with teams across all CMC-related units and management for coordination and communication.
Communication Skills
* Proficiency in English required; Mandarin is a plus.
* Excellent verbal, written, and presentation skills.
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