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Salary
$79k – $158k per year (Estimated)
Location
Remote/Hybrid (Indianapolis, United States)
Seniority
Senior · 15+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
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:

As a Senior Research Scientist in Analytical Development, you will be a key scientific leader on our Technical Development (TD) team, directly contributing to Elanco's mission by advancing the analytical and dissolution control strategies for our small molecule portfolio. In this role, you will be responsible for supporting our drug development pipeline through a diverse range of analytical activities, ensuring our new animal health products meet global quality and regulatory standards.

Your Responsibilities:

  • Develop, validate, and deliver robust analytical and dissolution methods and specifications, while driving the evaluation and implementation of new technologies to advance our drug development process.

  • Interpret complex scientific data, draw relevant conclusions, and effectively report and present technical results to internal teams and at external scientific conferences.

  • Author and support the generation of international registration documents, partnering with manufacturing and regulatory colleagues to drive drug product commercialization and technical submissions to global health authorities.

  • Mentor and coach emerging technical talent within the analytical development function, fostering a culture of scientific excellence.

  • Ensure all activities are compliant with internal and external quality standards and guidelines, including GxP, SOPs, and HSE.

What You Need to Succeed (minimum qualifications):

  • Education: PhD in Analytical Chemistry, Pharmacy, Pharmaceutical Sciences, or a related field with a minimum of 5 years of experience in pharmaceutical development; M.S. in a related field with a minimum of 10 years of experience; or B.S. in a related field with a minimum of 15 years of experience.

  • Experience: Strong expertise in chromatographic (HPLC/UPLC), spectroscopic (UV/VIS), and dissolution method development (specifically with USP Apparatus II and IV).

  • Top 2 skills: Extensive knowledge of current quality and regulatory requirements for new drug products and a demonstrated track record of successful interactions with regulatory agencies (e.g., FDA/CVM, EMA) on analytical topics.

What will give you a competitive edge (preferred qualifications):

  • Significant experience in dissolution development and regulatory submissions.

  • Experience with mass spectrometry (MS) and other areas of analytical method development.

  • Proven scientific leadership skills combined with strong problem-solving and creative thinking abilities.

  • Demonstrated ability to collaborate and positively impact interdisciplinary and international teams.

  • Experience working in regulated environments (e.g., GMP).

Additional Information:

  • Travel: 10%

  • Location: Global Elanco Headquarters - Indianapolis, IN - Hybrid Work Environment

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 a 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

  • Flexible work arrangements

  • 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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