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Salary
$116k – $227k per year (Estimated)
Location
In office (United States)
Seniority
Senior · 5+ years exp
Employment
Full-Time
Overview
Company
Impact
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Elanco is an American animal health company headquartered in Greenfield, Indiana, that was founded in 1954. The company develops, manufactures, and markets a wide range of products for pets and farm animals, including vaccines, parasiticides, antibiotics, and nutritional health additives. Operating as a global leader in the industry, the firm serves veterinarians and food animal producers in more than 90 countries and is listed on the New York Stock Exchange.

At Elanco (NYSE: ELAN) - it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better - join our team today!

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

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. Partnering closely with Manufacturing, Quality, Engineering, IT, and other functions, this position provides leadership and structure to successfully deliver technical and operational projects.

Your 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.

Additional Information:

  • Location: Elwood, Kansas

Don’t meet every single requirement?

Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco, we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for this role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!

Elanco Benefits and Perks:

We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:

  • 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% 401K matching

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

Elanco may use automated tools, including AI, to support parts of our 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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