Lilly Jobs

Job Information

Lilly TSMS Sterility Representative in Indianapolis, Indiana

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.

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 39,000 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. #WeAreLilly

Position Brand Description:

The Scientist positions in the Technical Services / Manufacturing Sciences – Sterility Assurance Technology (TS / MS – SAT) group are positions that provide support for control of the site’s manufacturing facilities. The group develop and implement sterility assurance related initiatives, and provide technical leadership with regard to sterility assurance strategies.

Key Objectives / Deliverables:

  • Ensure site’s Environmental Monitoring, Aseptic Process Simulations, Facility Cleaning, Facility Sanitization, Sterility Assurance Risk Management, and other sterility assurance programs are followed at the manufacturing floor level.

  • Provide technical guidance to the Process Team for sterility assurance programs.

  • Create and review periodic review of environmental monitoring data.

  • Lead or provide technical support for root cause investigations for sterility assurance programs.

  • Use of sterility assurance risk management to evaluate existing, proposed manufacturing processes and associated controls with respect to the potential for introduction of microbial, endotoxin and particulate contamination.

  • Execute and assist in the development of process and facility monitoring strategies that focus on areas of highest microbial risk.

  • Lead site aseptic self-inspection program including communication of observations and recommendations for continuous improvement to manufacturing and support personnel.

  • Analyze microbial and manufacturing data using statistical principles to identify trends, process disruptions, and opportunities for continuous improvements.

  • Create, execute, review and / or approve technical documents related to sterility assurance programs.

  • Create, execute and / or review change controls related to sterility assurance programs.

  • Continually educate self and others to drive improvements and to remain current with regulatory expectations and industry trends.

  • Participate in continuous improvement projects to improve quality performance at the site.

  • Participate or provide guidance for sterility assurance programs during regulatory audits.

Additional Preferences:

  • Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.

  • Understanding of GMPs and applicable internal standards

  • Communication (oral and written) skills; technical writing skills

  • Teamwork / interpersonal skills

  • Experience with data trending and analysis

  • Analysis and problem solving skills

  • Quality orientation

  • Ability to effectively influence

Education Requirements:

  • Bachelors Degree in Microbiology, Biology or related scientific field (or equivalent work experience)

Other Information:

  • 8 hour days – Monday through Friday

  • Overtime may be required

  • Work in a dynamic and fast-paced environment

  • 5 – 10% Travel Required

  • Applicant will work in various areas within the Parenteral Site. Some allergens are present.

  • Applicant will be required to become aseptic certified and to enter in aseptic manufacturing areas for support of activities. Mobility requirements should be considered when applying for this position

  • On call rotation (by phone) may be required

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

DirectEmployers