Process Engineer – IAPI – Night Shift at Eli Lilly and Company

Indianapolis, 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

PharmaceuticalsIndustries

Requirements

Bachelor of Science Degree in Engineering
2+ years of pharmaceutical manufacturing (or equivalent), preferably in API
Ability to apply fundamental engineering principles to process understanding, problem solving and process improvement
Ability to function in a team environment
Effectively manage and prioritize competing priorities and to appropriately communicate verbally and in writing to various audiences
Available on call to address processing emergencies over the phone and at times return to the plant during off-hours
Experience with Change Management, Deviation Management, Periodic Reviews, Commissioning and Qualification, Routine Data Monitoring
Ability to apply statistical thinking concepts to the analysis of manufacturing processes
Visualize an operation/process and reflect it in a model
Root cause analysis and the problem solving
Process Hazard Identification/Mitigation Skills
Strong Computer skills in a variety of software packages (Batch Plus, JMP, Visio, PI Data Historian, MS Project, Excel)
Experience with normal processing equipment/unit operations

Responsibilities

Provides technical oversight of the process equipment and ensures that the equipment remains in a qualified state to support the manufacture of bulk drug substance
Acts as equipment owner integrating process, process safety, environmental requirements and equipment knowledge
Monitors established equipment systems for process indicators to identify potential issues affecting production
Investigates and resolves equipment performance issues
Serves as technical expert/support for installation and maintenance of process equipment and equipment improvements
Develops training/tools for operations to transfer knowledge of equipment capabilities and operational techniques to operations and maintenance
Identifies/Implements improvement projects for capacity, product quality, raw material cost, emissions/waste loads, process variability and process safety
Performs and summarizes improvement opportunities in technical reports
Understands process/unit capacity constraints
Leads or participates in equipment/process qualification activities (including commissioning activities of new equipment or areas)
Provides technical leadership and problem solving skills for Health, Safety and Environmental incident investigations
Performs compliance related technical tasks such as emissions calculations, equipment evaluation, and application of material balances for env needs
Leads and/or participates in process hazard reviews and other process safety activities, main resource for process safety issues on supported processes
Manages the implementation of countermeasures arising from deviations, spills, and safety related events
Manages the implementation of recommendations from PHRs and other audit findings
Maintains training compliance
Maintains and establishes the equipment technical information for the process (Equipment procedures, P&IDs, Material of Construction Compatibility Index, Equipment information in PFDs, Aspen models, Material & Energy Balances, Process Safety Information)

Skills

Key technologies and capabilities for this role

Process EngineeringEquipment MaintenanceProcess SafetyEnvironmental ComplianceTroubleshootingEquipment QualificationProcess ImprovementTechnical ReportingTraining DevelopmentIncident InvestigationCommissioningCapacity Analysis

Questions & Answers

Common questions about this position

What are the basic qualifications for the Process Engineer role?

A Bachelor of Science Degree in Engineering and 2+ years of pharmaceutical manufacturing experience (or equivalent), preferably in API, are required.

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

This information is not specified in the job description.

What is the salary or compensation for this position?

This information is not specified in the job description.

What does Eli Lilly's company culture emphasize?

Eli Lilly unites caring with discovery to make life better for people, puts people first, and seeks determined individuals who give their best effort to discover life-changing medicines and give back to communities.

What additional preferences make a candidate stronger for this role?

Candidates with the ability to apply fundamental engineering principles to process understanding are preferred.

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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