Associate Director - Central Automation

Overview

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Eli Lilly, at our Indianapolis Parenteral Manufacturing facility, has a unique opportunity for vial, syringe and cartridge aseptic filling. Our Central Automation team is renowned within the parenteral network for its deep experience and ability to add value to our process teams. This Is an Exciting Opportunity To help lead that team and influence the business.

Key Objectives / Deliverables

• Lead the staffing, training, and leadership of the Indianapolis Parenteral Manufacturing Central Automation group, comprising nine individuals, to support multiple process teams with delivery, support, and lifecycle management.
• Manage compliance for the infrastructure supporting all process teams' automation needs, including HMIs/Data Historians/PLCs/HMIs/DCS/ Building Management Systems.
• Collaborate with Global Automation teams and parenteral networks to ensure filling lines comply with the latest supported software from a cybersecurity and data integrity perspective.
• Own and ensure compliance for IPM Automation Cybersecurity and Data Integrity.
• Influence the automation functional strategy across multiple plants within the IPM site.
• Support day-to-day engineering activities and plan for the 3-6 month horizon.
• Lead by example and coach others in safety, quality, engineering, and continuous improvement.
• Interact directly with regulatory agencies during site inspections.

Minimum Requirements

• Bachelors Degree in Engineering or Automation related field with a minimum of 5 years experience in a manufacturing environment.
• Technical competence in engineering, specifically automation and data architecture (Data Historians/LIFT/Database Management/PLCs/HMIs/DCS/ Building Management Systems).
• Experience in managing relationships with key vendors (Rockwell, BnR, etc.).

Additional Preferences

• Solid Understanding of Basic Requirements of Regulatory Agencies Such as the FDA, EMEA, DEKRA, And Osha in a GMP environment.
• Previous Experience with Highly Automated Equipment and OEM vendors as well as Industry leading Automation suppliers.
• Previous Experience in Supporting Parenteral Manufacturing Operations.
• Previous Equipment Qualification and Process Validation Experience.
• Previous Experience with Manufacturing Execution Systems and Electronic Batch Release.
• Previous Experience with Deviation and Change Management Systems Including Trackwise.

Other Information

• Standard business hours (days, M-F) with after-hour support and shutdown support as needed.
• Minimal travel required.
• Applicant will work in various areas within Indianapolis Parenteral where allergens may be present.
• 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 for further assistance. 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.

Actual compensation will depend on a candidates education, experience, skills, and geographic location. The anticipated wage for this position is $118,500 - $173,800 . Full-time equivalent employees also will be eligible for a company bonus and a comprehensive benefit program, including healthcare, 401(k), vacation, and other benefits.