Associate Director - Automation Engineering – Biologics at Eli Lilly and Company

Lebanon, Indiana, United States

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, BiotechnologyIndustries

Requirements

Minimum B.S. in Engineering and experience in Automation Engineering, preferably in Biologics manufacturing
10+ years working experience in Biopharma engineering, IT, operations, or manufacturing
Additional Preferences
Experience in design, development, commissioning and qualification of highly automated greenfield manufacturing sites utilizing SCADA, DCS and MES systems (DeltaV, Rockwell, Syncade, etc)
Experience as a member of the group leadership in running the plant, including participation in management sub-teams
Successful application of organizational models through recruiting and retention of employees

Responsibilities

Supervise and coach process control team, including completing performance reviews and development plans
Staffing, including recruiting, resource planning, and succession planning
Process control work coordination
Review and monitor financial performance; commit to meeting targets
Develop and implement the Automation Engineering Business Plan
Demonstrate a commitment to environmental, health, and safety
Identify, track, and report key indicators of functional performance
Ensure team is operating in a state of compliance
In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products
Assure focus by engineers and completion of critical assignments with appropriate monitoring and reporting
Instill teamwork within the department and demonstrate key interpersonal skills
Ensure appropriate technical depth and rigor with departmental technical deliverables
Make decisions independently and network with others as appropriate
Function in a team environment as a leader and as a member of management teams
Supervision of the process control engineers and consultants that support the daily operations of the Biologics facility
Ensure productivity and development of employees to maintain reliable and compliant control applications and systems in manufacturing
Partner to influence and implement within the process control organization and across functional disciplines to support the process control technical agenda, business plan priorities, and compliance objectives

Skills

Key technologies and capabilities for this role

Automation EngineeringProcess ControlBiologics ManufacturingGMP ComplianceLeadershipSupervisionStaffingRecruitingPerformance ReviewsSuccession PlanningResource Planning

Questions & Answers

Common questions about this position

What is the employment type for this position?

This is a full-time position.

Is this role remote or does it require on-site work?

This information is not specified in the job description.

What leadership and technical skills are required for this role?

The role requires strong supervisory and coaching skills for process control engineers, ability to ensure technical depth and rigor in automation deliverables, independent decision-making, and interpersonal skills to instill teamwork and network across functions.

What is the company culture like at Eli Lilly?

Eli Lilly emphasizes uniting caring with discovery, putting people first, and fostering collaboration, creativity, and resilience, especially as the site grows to full-scale GMP manufacturing.

What makes a strong candidate for this Associate Director role?

Strong candidates will have experience in administrative leadership like staffing and performance reviews, commitment to operational excellence in compliance and safety, and skills in building organizational capability through teamwork, technical rigor, and independent decision-making.

Eli Lilly and Company

Develops and delivers prescription medicines globally

About Eli Lilly and Company

Eli Lilly and Company is a global pharmaceutical company that focuses on discovering, developing, and delivering medicines to improve health. The company has a long history of scientific achievements, including the creation of insulin, the first life-saving treatment for diabetes. Lilly's operations involve extensive research and development to create new medications and enhance existing ones, ensuring they are safe and effective. Their products are primarily prescription medicines sold to healthcare providers for various medical conditions, including diabetes, cancer, and pain management. What sets Lilly apart from its competitors is its strong commitment to ethical practices and the protection of its products from counterfeiting. The company's goal is to enhance lives through innovative medical solutions while maintaining high standards of quality and ethics.

Indianapolis, IndianaHeadquarters

1876Year Founded

$1,180.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Competition from Novo Nordisk's Ozempic may impact tirzepatide's market share.

Potential construction delays in Indiana could affect GLP-1 drug production timelines.

Regulatory challenges may hinder Kisunla's expansion in new Alzheimer's markets.

Differentiation

Eli Lilly's rich history includes the first life-saving insulin treatment.

Lilly's strategic partnerships enhance its position in neurodegenerative disease treatments.

FDA approval of Zepbound opens new therapeutic markets for sleep disorder treatments.

Upsides

Lilly's $9 billion complex in Indiana boosts GLP-1 drug production capacity.

Kisunla's approval in China expands Lilly's Alzheimer's treatment market in Asia.

Collaboration with EVA Pharma enhances Lilly's reputation as socially responsible.

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