Associate Director - Central Automation

BioSpace

Indianapolis (IN)

On-site

USD 118,500 - 173,800

Full time

14 days+

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Benefits offered by this job

401(k) plan

Comprehensive medical benefits

Flexible spending accounts

Job summary

A global healthcare leader in Indianapolis seeks an Associate Director - Central Automation to lead a team ensuring compliance and leveraging automation strategies. Candidates must have a relevant degree, significant leadership experience, and expertise in automation technologies. The role is full-time with a competitive compensation range of $118,500 - $173,800, along with comprehensive benefits.

Qualifications

Minimum of 5 years experience in a manufacturing environment.
Must have a minimum of 3 years leadership experience.
Experience managing relationships with key vendors.

Responsibilities

Lead staffing and training of the Central Automation group.
Manage compliance for process teams' automation needs.
Support engineering activities and plan operational strategies.

Skills

Leadership

Automation expertise

Data architecture

Regulatory understanding

Education

Bachelor’s Degree in Engineering or Automation

Tools

Data Historians

PLCs

HMIs

Job description

Associate Director - Central Automation

Join to apply for the Associate Director - Central Automation role at BioSpace. Get AI-powered advice on this job and more exclusive features. 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.

Eli Lilly, at our Indianapolis Parenteral Manufacturing facility, has a unique opportunity for vial, syringe and cartridge aseptic filling. Eli Lilly as well as Indianapolis Parenteral Manufacturing are growing our footprint with recapitalizations as well as operating existing production lines. 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

Bachelor’s Degree in Engineering or Automation related field with a minimum of 5 years experience in a manufacturing environment.
Must have a minimum of 3 years leadership experience.
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.

Compensation and Benefits

Actual compensation will depend on a candidate’s 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 (depending, in part, on company and individual performance). 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.

EEO Statement

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 on 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.

Job Details