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Senior Manager/Associate Director, CMC Project Management, Peterborough
Client:
Location:
Peterborough, 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 at 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 projects.
- Establish project objectives, timelines, and deliverables. Define project tasks and resource requirements.
- Monitor and control project progression to ensure completion on schedule and within budget. Report progress to stakeholders.
- Support the technical team in investigating project challenges using risk assessment tools & techniques, and implement corrective measures.
- Manage communication with client contacts, organize project team meetings, and serve as liaison.
- Represent the company in project meetings, prepare agendas and minutes, and follow up on action items.
- Evaluate project results and recommend improvements.
- Support business development activities such as customer visits, conferences, and tradeshows.
- Prepare quotations, proposals, and change orders with input from stakeholders.
Qualifications
Education and Experience:
- Master's (MS) or PhD in life sciences; chemistry preferred
- At least 10 years of pharmaceutical or CRO/CMO industry experience, preferably in API or Drug Product R&D and manufacturing.
- Experience in project management or managing external research collaborations; PMP certification desired.
- Strong project management, problem-solving, and interpersonal skills; proven cross-functional work experience.
- Good understanding of pharmaceutical industry and small molecule drug development.
- Minimum 5 years relevant experience in CMC process development or GMP manufacturing.
- Knowledge of current regulations and industry trends; experience with oligonucleotides and solid-state peptides is a plus.
- Experience in CRO or CMO is preferred but not required.
- Proficiency in MS Office, especially MS Project.
Independence/Accountability
- Self-starter, motivated, flexible, with ~25% travel.
- Organized and detail-oriented.
- Proven problem-solving skills.
Leadership Activities
- Coordinate efforts across CMC units and with STA management for effective communication.
Communication Skills
- Fluent in English; Mandarin is a plus.
- Excellent verbal, written, and presentation skills.