Technical Project Manager, Technical Services / Manufacturing Sciences (TS/MS)

Your Role

The TSMS Technical Project Manager is responsible for coordinating cross-functional projects within the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility. This role ensures alignment with scientific, regulatory, and business objectives while managing timelines, resources, and project execution.

Responsibilities

• Develop and maintain detailed project plans, including scope, timelines, milestones, and resource allocation to ensure successful project delivery.
• Drive execution of cross-functional project plans, proactively identifying risks and developing mitigation and contingency strategies to ensure project success.
• Collaborate with internal teams, external partners, and vendors to achieve project objectives while maintaining alignment across all stakeholders.
• Communicate project status, risks, and key updates clearly and effectively to stakeholders and leadership.
• Partner with cross-functional teams to identify strategic and operational challenges that may impact project execution and develop solutions to address them.
• Act as a liaison between TS/MS, R&D, Operations, and other business functions, tailoring communication for both technical and non-technical audiences.
• Gather inputs and coordinate activities to develop and execute manufacturing project plans for development and commercial programs.

What You Need to Succeed (minimum qualifications)

• Education: Bachelor’s or Master’s degree in Science, Engineering (Mechanical, Chemical), Pharmaceutical Technology, or a related field (or equivalent experience).
• Experience: 5+ years of experience in the pharmaceutical or biotech industry, including at least 2 years of project management experience.
• Top 2 Skills: Strong project management and organizational skills with the ability to manage timelines, resources, and risks; and the ability to collaborate cross-functionally and communicate effectively with both technical and non-technical stakeholders.
• Working knowledge of cGMP standards and regulatory requirements, with proficiency in project management tools such as MS Project, Excel, and PowerPoint.

What will give you a competitive edge (preferred qualifications)

• PMP certification or equivalent project management training.
• Strong attention to detail with high personal standards for quality and ethics.
• Proven ability to build and maintain strong cross-functional relationships across all levels of the organization.
• Working knowledge of USDA, FDA, and EU GMP regulations for veterinary biologics.