Sr. Director - HSE at Eli Lilly and Company

Richmond, Virginia, United States

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Not SpecifiedCompensation

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

Full TimeJob Type

UnknownVisa

Pharmaceuticals, Biotechnology, ManufacturingIndustries

Requirements

Bachelor’s Degree in relevant discipline
5+ years of experience leading HSE teams and programs (preferably with PSM experience)
Additional Preferences
Proven leadership of HSE programs and management systems in manufacturing, including Process Safety Management (PSM)
Experience implementing and managing environmental compliance programs, including Title V reporting and recordkeeping
Skilled in engaging with regulatory agencies on environmental, health, and safety matters
Strong ability to build effective relationships

Responsibilities

Pre-Startup and Startup Phase:
Lead collaboratively and inclusively across all aspects of operational readiness and startup
Build an HSE organization with the capability, capacity, and culture to support safe, compliant, and efficient operations
Define HSE priorities and roadmap; implement systems and processes using internal expertise and external best practices
Establish and lead the site HSE Lead Team, embedding safety and environmental focus throughout project delivery and startup
Serve as a key HSE stakeholder during project execution—guiding design, startup planning, and contractor safety in partnership with Global Facilities Delivery
Develop and scale the HSE organization to support full GMP manufacturing, including environmental and PSM capabilities
Build strong technical partnerships with corporate/global teams and lead site-level execution of strategic initiatives
Post Startup:
Own the HSE Management System to ensure compliance with regulations and Lilly Global standards
Define and manage HSE priorities, roadmap, business initiatives, metrics, and the HSE Plan in collaboration with functional partners
Ensure ongoing compliance with reporting and recordkeeping requirements, including Title V
Benchmark best practices across the Lilly network and external industry
Develop future HSE leadership for both site and global roles
Escalate critical HSE issues to site and corporate leadership as needed
General:
Develop, implement, and maintain HSE programs and systems at the Lilly manufacturing site, including oversight of all site operations—manufacturing, labs, utilities, waste, emergency response, and administrative areas—ensuring compliance with global and regulatory standards
Lead the site HSE team, supports employee development, and serves as the primary liaison with corporate HSE to ensure alignment and readiness for regulatory inspections
As a member of the Lilly Site Lead Team, contribute to strategic planning and cross-functional leadership

Skills

Key technologies and capabilities for this role

HSEGMPRegulatory ComplianceEmergency ResponseRisk ManagementLeadershipStrategic PlanningEmployee DevelopmentManufacturing SafetyBiopharmaceuticals

Questions & Answers

Common questions about this position

What is the employment type for this Sr. Director HSE role?

The position is full time.

Where is this job located?

The role is at Lilly's manufacturing site in Goochland County, Virginia.

What are the key responsibilities during the pre-startup and startup phase?

Key responsibilities include leading operational readiness, building the HSE organization and culture, defining HSE priorities and roadmap, establishing the site HSE Lead Team, guiding design and contractor safety, and developing environmental and PSM capabilities.

What is the company culture like at Lilly for this role?

The role involves building the organization, facility, and culture to enable a successful startup into GMP manufacturing operations, with an emphasis on collaborative and inclusive leadership, putting people first, and embedding safety and environmental focus.

What makes a strong candidate for the Sr. Director HSE position?

Strong candidates will have leadership experience in HSE for manufacturing startups, ability to build teams and systems for GMP compliance, and skills in strategic planning as a member of the Site Lead Team.

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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