Senior Manager (Associate Director) CMC Project Management

About the role

The Senior Project Manager (or Associate Director, depending on qualifications) 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. This is a remote (work from home) position within the US and requires English and Mandarin language skills.

Responsibilities

• Lead all project initiation and planning efforts. Participate in the implementation and execution of a given project.
• Establish project objectives, timelines, and deliverables. Defines project tasks and resource requirements.
• Closely monitor/control project progression to ensure the project is completed on schedule and within budget. Reports project progress to all key stakeholders.
• Support the technical team to investigate any project challenges by using necessary risk assessment tools & techniques, then implements corrective measures.
• Serve as liaison with client contacts, manages day-to-day communications and organizes project team meetings.
• Represent the company in project meetings, prepares meeting agenda and minutes, and follows up on action items.
• Evaluate and assess project results and provides recommendations for future improvements.
• Provide support to the business development team by joining customer visits, conferences, or trade shows.
• Contribute to Proposals and timelines with inputs from key stakeholders for new client relationships and change orders for existing client relationships.

Qualifications

• Master's (MS) or PhD in life sciences; chemistry preferred
• A minimum of 4 years of 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 and a proven track record working cross-functionally across a wide variety of technical, business, and operational areas
• Demonstrates a 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
• Working knowledge and understanding of current regulations and industry trends for small molecule, manufacturing, and testing. Oligonucleotide and Solid State Peptide experience a plus
• Experience in a Contract Research Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred, but not required
• Working knowledge of MS Office products, especially MS Project
• Must be a self-starter, self-motivated, and highly flexible in this home based position with ~25% travel
• Must be organized and detail-oriented
• Proven experience in creating and carrying out successful plans and processes to solve complex problems
• Work closely with team members across all CMC-related business units and with the STA management team to ensure coordination of all efforts and real-time communication with all stakeholders
• Proficiency in both English and Mandarin is required
• Excellent communication skills (verbal, written, and presentation skills)