Join American pharmaceutical leader Eli Lilly and Company, currently hiring Scientist TS/MS Sterility Assurance Technology in Indianapolis, Apply Lilly careers in Indianapolis Indiana.
Position : Scientist TS/MS Sterility Assurance Technology
Location : Indianapolis, Indiana
Job id: R-34301
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:For 140 years, Lilly has manufactured medicines that improve people’s lives around the world. We produce our medicines using some of the most sophisticated manufacturing technologies and rigorous quality standards. Lilly Manufacturing strives for excellence in its process, standards, procedures and behaviors to develop medicines with safety first and quality always.Position Brand Description:The Scientist, Sr. Scientist, and Associate Consultant 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.Basic Qualifications: Bachelors Degree in Microbiology, Biology or related STEM fieldAdditional Preferences:Experience with data trending and analysisAnalysis and problem solving skillsQuality orientationAbility to effectively influenceResponsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.Understanding of GMPs and applicable internal standardsCommunication (oral and written) skills; technical writing skillsTeamwork / interpersonal skillsOther Information: 8 hour days – Monday through FridayOvertime may be requiredWork in a dynamic and fast-paced environment5 – 10% Travel RequiredApplicant 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 positionOn call rotation (by phone) may be requiredEli 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 ( Lilly_Recruiting_Compliance@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.Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.
As a condition of employment with Eli Lilly and Company and its subsidiaries in the United States and Puerto Rico, you must be fully COVID-19 vaccinated and provide proof of vaccination satisfactory to the company (subject to applicable law). #WeAreLilly
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