Advisor - Engineering - IDM at Eli Lilly and Company

Indianapolis, Indiana, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, HealthcareIndustries

Requirements

Senior technical expertise in engineering, particularly in device assembly, automated processes, and manufacturing platforms
Experience with Design for Manufacturability (DFM) reviews and influencing R&D teams on component designs compatible with automated assembly
Knowledge of tolerances, orientation features, materials, part interaction, and feeding for production scale
Proficiency in leading requirements generation, pFMEA, control strategies, and patient risk mitigation from equipment design
Ability to generate/interpret Assembly Process Specifications for automated equipment design
Experience working with project teams to select equipment OEMs and represent engineering in Due Diligence for business development
Capability to identify and introduce new device assembly process technologies to optimize capital and time-to-volume
Skills in supporting assembly technology development, de-risking/proof-of-concept work, and developing business cases for technologies
Mentoring experience, especially for recent grads and project technical leads
Expertise as SME in technical studies, troubleshooting major issues during debug/qualification, and participating in design reviews
Global troubleshooting support for operating assembly lines and participation in Post Launch Optimization Teams
Ability to maintain relationships with platform Engineering and Operations associates and inventory of platform technology/control strategies

Responsibilities

Provide technical leadership for scope development, design, delivery, and optimization of Device Platform for IDM and Device network, new product commercialization, capacity expansion, and operations
Identify and ensure requirements for new products and processes, focusing on automated process assembly
Lead manufacturing platform consistency and continuous improvement; serve as responsible engineer per local quality practices
Perform Design for Manufacturability reviews; consult/influence Device R&D on compatible component designs
Assure tolerances, orientation features, materials, part interaction, and feeding are appropriate
Lead/facilitate requirements, pFMEA, and control strategy generation; mitigate patient risks from equipment design
Generate/interpret Assembly Process Specification for automated assembly equipment design
Work with project teams to select equipment OEMs
Represent engineering in Due Diligence for business development
Identify/introduce new assembly process technology strategies
Support/influence assembly technology development initiatives
Assist/lead de-risking/proof-of-concept for new processes/technologies
Develop business cases for technology applications
Mentor technical team members, focusing on recent grads and project leads
Consult on technical strategies, risks, and mitigation for project teams
Initiate/support proof-of-principle with OEMs and CTC
Serve as SME in technical studies for project delivery
Troubleshoot major issues during asset debug/qualification
Participate in design reviews for high-risk systems
Review/approve technical study strategies and consult on results interpretation
Provide global troubleshooting support for escalated assembly line problems
Participate in platform Post Launch Optimization Team meetings
Serve as identified responsible engineer for platform
Maintain relationships with platform Engineering/Operations at assembly sites
Maintain inventory of platform assembly technology and control strategies

Skills

Design for Manufacturability

Automated Process Assembly

Device Platform

Manufacturing Optimization

Commercialization

Process Design

Continuous Improvement

Technical Leadership

Device R&D

Quality Engineering

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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