Associate R&D at Elanco in greenfield, Indiana

Job Description:

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. We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.

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: Analytical Development and Quality Control R&D Associate

This laboratory-based role will be a member of the Small Molecule Technical Development Group (SMTD) responsible for the analytical testing and characterization of the Elanco small molecule development portfolio. The analytical chemist will collaborate closely with colleagues to plan and execute laboratory-testing experiments across a variety of analytical techniques, as required.  This role will include assisting in the interpretation and recommended changes to scientific protocols and procedures, basic analytical method development, fit for purpose method qualification, execution of compendial test methods, support of stability studies, and generation of other analytical data as needed.

Your Responsibilities:

• Perform characterization of pharmaceutical materials utilizing a variety of analytical techniques (HPLC/UPLC, Karl Fischer titration, Dissolution, etc.).


• Employ good documentation practices in a timely manner.


• Evaluate, interpret, and verify analytical data, including second person verification of other analysts’ work.


• Prepare necessary reagents and solutions, maintain necessary consumables and laboratory supplies, including placing purchase requisitions, as needed.


• Maintain laboratory equipment according to local procedures, as necessary. Ensure preventative maintenance and calibrations are executed on time and as planned.


• Use proper safety equipment and follow appropriate safety procedures.


• Ensure proper handling and disposal of biohazard materials and/or hazardous chemicals.


• Assist in authoring laboratory method procedures, validation protocols and reports, and other GMP documents.  


• Utilize problem-solving/troubleshooting skills to investigate laboratory issues and identify root causes.


• Execute and document laboratory investigations appropriately when necessary.


• Provide technical training to other analysts and cross train on other techniques as required to meet business needs.


• Maintain compliance with company, site and regulatory policies and procedures.


• Work collaboratively between groups to ensure support is being optimized to meet business requirements.


• Actively participate in planning and troubleshooting meetings in order to find effective solutions for workload planning and analytical investigations.


• Maintain appropriate scheduling and planning to ensure analytical work is executed within given timelines.


• Perform other duties as assigned.

What You Need to Succeed (minimum qualifications): 

Education: Bachelor’s degree in chemistry, Biology, Engineering, or other applicable scientific discipline.

Required Experience:

• Previous 1-5 years of experience working in a pharmaceutical laboratory.


• Strong working knowledge of analytical laboratory operations with a focus on analytical chemistry.


• Demonstrated experience utilizing HPLC/UPLC, KF, Dissolution and other common techniques within a pharmaceutical testing laboratory.


• Knowledge of analytical method validation and qualification, as per applicable guidelines.


• Knowledge of good documentation practices, including usage of an electronic notebook system.


• Adaptable and flexible mindset with a strong problem solving ability.


• Ability to work collaboratively as well as independently to achieve goals.


• Self-starter with excellent written and verbal communication.
   

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

• Previous experience authoring analytical method procedures, protocols, and technical reports, desirable.


• Previous experience using an electronic document management system (EDMS), such as Veeva QDocs.


• Previous experience utilizing an electronic Quality Management System such as Veeva QMS


• 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.

Other Information:

• Expected Travel : Less than 10%


• Location: Global Elanco Headquarters - Greenfield, IN

Don’t meet every single requirement? Studies have shown underrepresented 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