Your Role: TSMS Technical Project Manager
Responsible for coordinating cross‑functional projects within the Elwood, Kansas monoclonal antibody manufacturing facility, ensuring alignment with scientific, regulatory, and business objectives while managing timelines, resources, and execution.
Your Responsibilities
- Develop and maintain detailed project plans, including scope, timelines, milestones, and resource allocation.
- Drive execution of cross‑functional project plans, proactively identifying risks and developing mitigation and contingency strategies.
- Collaborate with internal teams, external partners, and vendors to achieve project objectives while maintaining stakeholder alignment.
- 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 and develop solutions.
- Act as a liaison between TS/MS, R&D, Operations, and other business functions, tailoring communication for 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 related field (or equivalent experience).
- Experience: 5+ years in the pharmaceutical or biotech industry, including at least 2 years of project management experience.
- Key Skills: Strong project management and organizational skills, ability to manage timelines, resources, and risks; cross‑functional collaboration and effective communication with both technical and non‑technical stakeholders.
- Working knowledge of cGMP standards and regulatory requirements; proficiency in MS Project, Excel, and PowerPoint.
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.
- Working knowledge of USDA, FDA, and EU GMP regulations for veterinary biologics.
Location
Elwood, Kansas
Benefits
- Multiple relocation packages.
- Two weeklong shutdowns (mid‑summer and year‑end) in the US (in addition to PTO).
- 8‑week parental leave.
- 9 Employee Resource Groups.
- Annual bonus offering.
- Up to 6% 401(k) matching.
EEO Statement
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Recruitment Process Note
Elanco may use automated tools, including AI, to support parts of the recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
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