Principal Process Safety Engineer (NOT REMOTE - NEW SITE)

Chester, Maryland, United States

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Not SpecifiedCompensation

Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, Healthcare, BiotechnologyIndustries

Requirements

A Bachelor's degree in chemical engineering, chemistry, or a related field is required, with CCPSC or PE preferred. Candidates must have 3+ years of experience in chemical or pharmaceutical manufacturing and possess knowledge of OSHA Process Safety Management (PSM) regulations. Additional preferences include CCPSC or PE certification, training in Process Hazard Analysis (PHA), HAZOP, and What-If Methodologies, strong analytical and collaboration skills, training in Layer of Protection Analysis (LOPA), and knowledge of EPA Risk Management Plans.

Responsibilities

The Principal Process Safety Engineer will provide technical leadership and engineering support for process safety management throughout the site's development, construction, and operational phases. Key responsibilities include supporting the PSM readiness plan, acting as a stakeholder in facility design and startup, overseeing PHAs and facility siting studies, developing and implementing core PSM elements, training staff on process safety, overseeing API manufacturing operations, partnering with other departments to manage change and ensure safe systems, and ensuring compliance with industry codes and standards. The role also involves building technical relationships with corporate and external process safety groups.

Skills

Process Safety Management

Process Hazard Analysis

HSE

GMP Manufacturing

API Manufacturing

Facility Design

Construction

Startup Operations

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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