Senior Specialist OJT B108 Control Inspection in Indianapolis

Job Description

Join American pharmaceutical leader Eli Lilly and Company, currently hiring Senior Specialist OJT B108 Control Inspection in Indianapolis, Apply Lilly careers in Indianapolis Indiana.

 

Position : Senior Specialist OJT B108 Control Inspection

Location : Indianapolis, Indiana

Job id: R-33658

 

Job Details

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.

Responsibilities:The Operations Senior Specialist will be responsible for performing On The Job training for employees within the Central Inspection space. The Operations Senior Specialist – OJT will play a key role in ensuring that new employees are appropriately trained to be able to effectively execute necessary tasks associated with manufacturing and inspection related activities, as well as helping to ensure existing employees are within qualification status for activities within the area. Further responsibilities and objectives include:Organize onboarding process for new employees to the inspection area.Work with area supervision to understand qualification statuses of employees.Coordinate qualification and or re-qualification needs and execution with individuals and area leadership.Partner with process team and area leadership to help develop associated process improvements.Provide additional documentation and data gathering support to Senior Specialist responsible for Production Ticket Auditing.Provide additional production support when required.
Basic Requirements:High School diploma/GEDQualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
Additional Skills/Preferences:Parenteral Manufacturing ExperienceExperience in a GMP manufacturing settingDemonstrate good documentation practicesPMX and SAP experienceProficient in PMXCompletion of Post Offer Exam or Completion of Work Simulation if applicable.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 ( 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.

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).

 

 

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