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Lilly Analyst I–Technical Services/Manufacturing Services(TS/MS) Process Data - FDE in Branchburg, New Jersey

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Organization Overview

At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing, and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medicines, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.

Path/Level:

P1

General Summary:

Entry level position responsible for ensuring the accuracy of data and providing data analysis support for data generated during manufacturing processing at the Lilly Branchburg, NJ site. This position will interact with the manufacturing, quality assurance and quality control departments. Some interaction with other Lilly sites or contract manufacturers may be required. Knowledge of cell culture, purification and support systems is a plus. Spreadsheet experience required, database experience a plus.

Responsibilities:

  • Verifies the accuracy of the data entered into the in-process database by the operations staff and ensures that all the data entries are complete.

  • Assists with the trending and analysis of manufacturing production data to support: deviations, process validation protocols and reports, technology transfer documentation, BLA filings, annual manufacturing summaries for regulatory documentation, etc.

  • Assists with the maintenance of local databases.

  • When requested, provides data for technical reports supporting technology transfers, deviation/adverse event reporting and process analysis/trending.

  • May lead small to medium-scale projects or programs. Makes decisions that impact own priorities and allocation of time to meet deadlines.

  • Provides sound problem solving skills to complex issues.

  • Writes SOPs as they relate to the activities of the TS/MS group. May assist with SOPs from other manufacturing groups.

  • Understands and performs all job responsibilities in compliance with safety and regulatory expectations, as well as, cGMP.

Basic Requirements:

  • Bachelor of Science degree in a scientific or engineering discipline with 0 - 3 years of relevant experience

Additional Skills/Preferences:

  • Strong mathematical and analytical skills

  • Excellent communication skills, both oral and written

  • WORD, EXCEL, and Powerpoint experience required, coding experience a plus

  • SQL database experience a plus

  • Experience in cell culture and/or protein purification manufacturing a plus

  • An understanding of current Good Manufacturing Practices a plus.

  • Familiarity with TrackWise and LIMS a plus

Additional Information

  • This position is not permanent. It is for a fixed term position up to a maximum of 4 years.

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( LillyRecruitingCompliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( LillyRecruitingCompliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly 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.

At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.​ We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!

#WeAreLilly

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