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 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.

Position Title:

PPM Lead Technician - QA

Position Type:

Full-Time

Job Level:

B4

Location:

Indianapolis, LTC-S

Job Function:

Quality Assurance

Position Posted:

     

Supervisor:

Sr. Manager or Assoc Director - Quality

Internal Posting Dates:

     

Position Brand Description:

The Printed Packaging Material - Quality Assurance Lead Technician will work in the Indianapolis Device Assembly & Packaging site where products for domestic and international markets are assembled and packaged. The primary purpose of the position is to provide daily support and technical oversight for the safety and inspection of high-quality printed packaging materials utilizing Lilly standards by following good manufacturing practices.  The Lead Technician works as a team member with a focus on leading the inspection of these materials and abiding by the Lilly culture of integrity, excellence, and respect for people.

Key Objectives / Deliverables:

Responsible for training and the completion of all requirements for the qualification of new Printed Packaging Material Inspection team membersServe as coach / mentor to QA Technician team to ensure continuous learning on quality processes and systemsSupport process improvements to help improve productivity within the local process team or quality organizationAssist the QA Team Leader with additional requests as neededReview and analyze Lilly printed packaging materials at incoming inspection according to standard operational procedures (SOPs).Utilize calibrated text verification system, databased computer systems, and measurement tools to perform inspection.Review production data for PPM batch releaseProvide support for the production area, as applicable, for issues arising around printed packaging materialsOrganize, critically review, and present information in accordance with written proceduresEnsure compliance with applicable procedures, cGMP's policies, and regulationsCommunicate effectively with customers and quality representatives to evaluate and reinforce requirementsApply experience and knowledge of cGMP requirementsWork independently on inspections ensuring that printed material inspections meet customer due dates and quality needsWork within QA Technician team to ensure all team members receive QA support needed to maintain daily operations

Management of Controlled Substances, if applicable:

Comply with all established requirements to receive and maintain authorization to handle controlled substances.Successfully complete the background check process.Complete the training assigned to your learning plan within the established due dates.Report drug diversion.Any employee who has knowledge of drug diversion from his employer by a fellow employee has an obligation to report such information to a responsible security official of the employer, as established in the Code of Federal Regulations
CFR 1301.91.Report illicit activities by employees:You are responsible under state, federal and local law, and Lilly policy to report to your supervision and Global Security any irregular or unauthorized employee activities involving controlled substances / drugs (e.g., unauthorized or illicit possession, manufacture, use, distribution, theft, diversion, or destructions), as established in the Code of Federal Regulations 21 CFR 1301.92.

Minimum Requirements:

IDAP PPMQA inspection experienceAt least two years of pharmaceutical manufacturing experienceMust be able to pass vision screeningProficiency with applicable computer systemsStrong oral and written communication and interpersonal skillsStrong attention to detailAbility to work with constant changes, time pressure, interruptions, and distractions

Additional Preferences:

Experience with cGMP’sProven ability to take initiative, work independently or as part of a team to resolve an issue

Education Requirements:

High school graduate or equivalent.  

Other Information:

Ability to work 8-hour days – Monday through Friday on site.Ability to work overtime as required.Tasks require repetitive motion for long periods of time.Applicant will work in various areas within a manufacturing site.  Allergens are likely in the manufacturing environment.  Mobility requirements and exposure to allergens should be considered when applying for this position.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, 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 are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$28.12 - $46.88

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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