Elanco Animal Health

Associate Scientist - Cell Line Development

Elanco Animal Health$70K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s or Master’s degree in a relevant scientific discipline with significant industry experience.
  • Expertise in mammalian suspension cell culture, specifically CHO and 293 cells.
  • Strong troubleshooting skills, capable of analyzing complex data.
  • Ability to manage multiple projects in a fast-paced environment.

Responsibilities

  • Develop and optimize workflows for mammalian cell culture and cell line generation.
  • Oversee the creation of stable and clonal cell lines for vaccine candidates.
  • Act as a technical expert, collaborating across various scientific teams.
  • Implement new technologies to improve the cell line development process.
  • Maintain data integrity by drafting technical protocols and reporting findings.

Benefits

  • Multiple relocation packages
  • Two weeklong shutdowns (mid-summer and year-end) in addition to PTO
  • 8-week parental leave
  • 9 Employee Resource Groups
  • Annual bonus offering
  • Flexible work arrangements
  • Up to 6% 401K matching
Full Job Description

Your Role: Senior Associate Scientist, Cell Line Development

As a Senior Associate Scientist, Cell Line Development, you will be a pivotal member of our Transitional and Early Development (TED) team, directly contributing to the advancement of Elanco’s biotherapeutic and vaccine pipeline. You will leverage your deep expertise in mammalian cell culture, molecular biology, and biochemistry to develop and industrialize next-generation cell lines. This is a hands-on laboratory role where you will take ownership of projects, collaborate with a diverse group of scientists, and see your work translate from research to development, making a tangible impact on animal health.

Your Responsibilities:

  • Guide the development, optimization, and implementation of robust workflows for mammalian cell culture and high-performance cell line generation.
  • Take ownership of the end-to-end creation of stable and clonal cell lines for biotherapeutic and vaccine candidates, utilizing advanced platforms such as Beacon and VIPS.
  • Serve as a key technical matter expert on cell line development, providing critical scientific input and fostering seamless collaboration with Discovery, Upstream Process Development, and Analytical teams.
  • Manage the evaluation and implementation of new technologies and methodologies to enhance the speed, quality, and efficiency of our cell line development engine.
  • Ensure meticulous data integrity and knowledge transfer by authoring detailed technical protocols, analyzing complex datasets, and clearly presenting scientific findings to guide project progression.

What You Need to Succeed (minimum qualifications):

  • Education: Bachelor’s Degree in a relevant scientific discipline (e.g., Molecular Biology, Cell Biology, Biochemistry, Biotechnology) with at least 6 years of industry experience, OR a Master's degree with at least 3 years of industry experience.
  • Experience: Deep technical expertise in mammalian suspension cell culture (specifically CHO and 293 cells), including aseptic technique, media preparation, and cell banking.
  • Top Skills: Proven ability to independently troubleshoot complex technical issues, interpret complex data to influence project direction, and effectively manage multiple projects in a fast-paced, collaborative environment.

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

  • Demonstrable hands-on experience in the end-to-end development of stable cell lines, including transfection, single-cell cloning, and characterization of clonality and stability.
  • Proven project management experience with the ability to guide technical strategy and mentor junior scientists.
  • Hands-on experience with high-throughput cell line development platforms (e.g., Beacon, VIPS) and flow cytometry.
  • A strong understanding of upstream bioprocess techniques, including the use of shake flasks, ambr®, and bench-scale bioreactors.
  • Familiarity with cGMP principles and the regulatory requirements for cell line development and characterization for IND/BLA submissions.

Additional Information:

  • Travel: Up to 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

About Elanco Animal Health

Elanco Animal Health is an American pharmaceutical company that develops and produces products for animal health. The company was founded in 1954 and is headquartered in Greenfield, Indiana. Elanco produces a wide range of products for both livestock and pets, including vaccines, antibiotics, and parasiticides. The company operates in more than 90 countries and has a global workforce of over 5,500 employees. Elanco was spun off from Eli Lilly and Company in 2018 and became a publicly traded company in September of that year. The company is listed on the New York Stock Exchange under the ticker symbol ELAN.
Learn more about Elanco Animal Health
Size
9,000 employees
Market Cap
$5.3 billion
Industry
Net Income
-$560 million
5 Year Trend
+10.3%
Revenue
$3.2 billion
NASDAQ

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