Area Engineer - Small Molecule Building Lilly Medicine Foundry at Eli Lilly and Company

Lebanon, Indiana, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, Healthcare, BiotechnologyIndustries

Requirements

Be the SME with deep technical expertise in all systems under responsibility, including understanding applications in pharmaceutical manufacturing, flow charts, process parameters, and industry trends
Expertise in specific building systems: API Reactor Suite(s) (fixed reactors and condensers 50–500 gallons, Agitated Filter Dryers (AFD), Temperature Control Units (TCU’s), Solvent Filtering and Distribution), High Potency API Production (HPAPI) (Level III containment, ISO 8 environment, Isolators and portable tanks), Experimental Materials Lab (EML) (Downflow booths, Walk-In/bench top fume hoods, Temperature Control Units (TCU’s)), Purified Water w/ Endotoxin Control (PWEC), Bulk solvent distribution within the SMB, Gray/clean utility distribution within the SMB, Primary and Secondary waste streams within the SMB
Ensure assigned processes are aligned with Industry and Lilly Standards
Support risk assessment exercises using tools like FMEA
Participate in teams, committees, or groups to achieve FUME’s departmental, site, and/or company goals

Responsibilities

During project phase: Assist in design, construction, commissioning, qualification, start-up, and operational readiness of all systems in the SMB as part of cross-functional project team
During day-to-day operations: Oversee and maintain SMB and associated ancillary systems effectively, reliably, and cost-consciously, keeping them in compliance, in-control, and fit for use
Drive continuous improvement initiatives
Manage annual local operating and capital expenditures (CAPEX) for revisions, new functionality, or capacity
Act as single point of contact for all residents/customers associated with the SMB
Lead or participate in projects/changes for SMB systems, including design and verification activities (IV/OV/PQ), as user representative for capital projects or delivery agent for local projects
Develop documentation (URS, test cases, etc.) to demonstrate systems are properly installed, qualified, started up, and remain in a state of control
Contribute to process resource assessment and capital plans

Skills

Engineering

Facilities Management

Utilities Maintenance

System Design

Construction

Commissioning

Qualification

Start-up

Operational Readiness

Compliance

Continuous Improvement

Small Molecule Manufacturing

GMP

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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