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Director Pharmaceutical Manufacturing Jobs (NOW HIRING)

$170 - $200/hr

Overview We are seeking a Health, Safety & Environment (HSE) Director to join our Pharmaceutical Manufacturing in TX, AL, VA, PA, OH, IN, and WI. Our Pharmaceutical team is growing! The Health ...

$170 - $200/hr

It is a unique opportunity to help shape and lead one of the largest pharmaceutical manufacturing ... Proven ability to influence across large matrixed organizations without direct authority.

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How much do director pharmaceutical manufacturing jobs pay per year?

As of Sep 7, 2026, the average yearly pay for director pharmaceutical manufacturing in the United States is $141,872.00, according to ZipRecruiter salary data. Most workers in this role earn between $111,500.00 and $167,000.00 per year, depending on experience, location, and employer.

What does a director of pharmaceutical manufacturing do?

A Director of Pharmaceutical Manufacturing oversees the entire manufacturing process of pharmaceutical products, ensuring that operations comply with regulatory standards and quality requirements. They are responsible for managing production teams, optimizing manufacturing processes, and implementing safety and efficiency improvements. This role also involves coordinating with other departments such as quality assurance, research and development, and supply chain management to ensure timely and cost-effective production. The director plays a critical role in maintaining product quality, meeting production goals, and adhering to industry regulations.

What are the key skills and qualifications needed to thrive as a director of pharmaceutical manufacturing?

To thrive as a Director of Pharmaceutical Manufacturing, you need extensive knowledge in pharmaceutical production, regulatory compliance, quality assurance, and a degree in pharmacy, chemistry, or engineering—often complemented by advanced degrees or industry certifications. Familiarity with Good Manufacturing Practices (GMP), ERP systems, process automation technologies, and regulatory frameworks like FDA or EMA guidelines is crucial. Leadership, strategic planning, problem-solving, and strong communication skills distinguish top performers in this role. These abilities are vital to ensure product quality, operational efficiency, regulatory adherence, and the successful management of complex manufacturing teams.

What are some common challenges faced by a director of pharmaceutical manufacturing, and how are they typically addressed?

Directors of Pharmaceutical Manufacturing often encounter challenges such as ensuring consistent product quality, maintaining regulatory compliance, and optimizing production efficiency. Addressing these issues requires strong leadership to implement robust quality systems, stay up-to-date with evolving regulations, and drive continuous improvement initiatives. Collaboration with cross-functional teams—including quality assurance, regulatory affairs, and engineering—is essential for problem-solving and achieving production goals. Proactive communication and a commitment to ongoing staff training also help mitigate risks and support a culture of operational excellence.
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Cities with the most Director Pharmaceutical Manufacturing job openings:

What are the most commonly searched types of Pharmaceutical Manufacturing jobs?

The most popular types of Pharmaceutical Manufacturing jobs are:

What states have the most Director Pharmaceutical Manufacturing jobs?

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Infographic showing various Director Pharmaceutical Manufacturing job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, 1% Temporary, and 1% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $141,872 per year, or $68.2 per hour.

Health, Safety & Environment (HSE) Director - Pharmaceutical Manufacturing

AtkinsRéalis

Richmond, VA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago


Job description

Job Description
Overview
We are seeking a Health, Safety & Environment (HSE) Director to join our Pharmaceutical Manufacturing in TX, AL, VA, PA, OH, IN, and WI.
Our Pharmaceutical team is growing! The Health, Safety & Environment (HSE) Director serves as the owner's senior HSE governance leader across a major pharmaceutical manufacturing campus. This role provides independent oversight of environmental, health, safety, and process safety performance across all contractors, construction managers, and EPC organizations. Unlike contractor-led safety positions, this role represents the owner's interests by establishing expectations, verifying compliance, monitoring performance, identifying systemic risks, and ensuring effective management of Process Safety Management (PSM) obligations throughout the project lifecycle. The position acts as the primary owner authority for HSE governance, contractor assurance, serious incident prevention, life-critical risk management, process safety oversight, regulatory compliance, and continuous improvement initiatives. Success in this role is measured by the effectiveness of HSE governance systems, contractor compliance performance, reduction of serious incidents and high-potential events, successful regulatory readiness, and achievement of industry-leading safety outcomes throughout design, construction, commissioning, startup, and operations readiness activities. This is a unique opportunity to help shape and lead one of the largest pharmaceutical manufacturing investments in North America while working alongside industry-leading professionals on a career-defining program on a greenfield campus. We are offering a full-time position with AtkinsRéalis that provides the opportunity to lead complex, high-profile programs, collaborate with world-class delivery teams, and receive a highly competitive compensation package with robust benefits.
Your role
  • Serve as the owner's senior HSE representative across all capital project activities, contractors, construction managers, and EPC organizations.
  • Establish, implement, and govern owner-side HSE standards, expectations, procedures, and assurance programs across the campus.
  • Lead development and execution of sitewide HSE governance frameworks to ensure alignment with Lilly requirements and regulatory obligations.
  • Oversee contractor compliance with project HSE requirements, environmental permits, regulatory requirements, and owner standards.
  • Monitor and evaluate contractor HSE performance through audits, assessments, inspections, observations, and assurance reviews.
  • Lead owner investigations of significant incidents, high-potential events, process safety concerns, and environmental non-compliance issues.
  • Oversee corrective action management programs and ensure timely closure of identified deficiencies and improvement opportunities.
  • Provide independent verification that contractor safety performance data, leading indicators, and lagging indicators are accurate and complete.
  • Establish and oversee life-critical risk management programs including working at height, confined space, lifting operations, energized work, excavation, and contractor control systems.
  • Lead Process Safety Management (PSM) oversight activities during design, construction, commissioning, startup, and operational readiness phases.
  • Ensure effective management of PSM elements including process hazard analysis, management of change, pre-startup safety reviews, operating procedures, mechanical integrity, and contractor safety programs.
  • Partner with engineering, operations, commissioning, CQV, startup, and project leadership teams to identify and mitigate process safety risks.
  • Participate in design and constructability reviews to ensure HSE and PSM requirements are incorporated into project execution strategies.
  • Facilitate HSE leadership reviews, executive governance meetings, and contractor performance evaluations.
  • Develop executive-level HSE dashboards, risk assessments, assurance reports, and performance metrics for owner leadership.
  • Monitor regulatory developments and ensure project compliance with applicable OSHA, EPA, environmental, and process safety requirements.
  • Support emergency preparedness, crisis management planning, incident response readiness, and contractor emergency response coordination.
  • Drive continuous improvement through lessons learned programs, trend analysis, and industry best-practice implementation.
  • Promote a culture of safety, environmental stewardship, risk awareness, accountability, and operational excellence across the project.
  • Build strong relationships with client leadership, regulatory stakeholders, contractor organizations, and project delivery teams.
  • Communicates on a regular basis with clients to assure satisfaction with services provided.
  • Directs risk management initiatives and supports enterprise-wide HSE improvement objectives.
  • Obtains client feedback and manages lessons learned processes to improve future program delivery.

About you
  • 20+ years of professional experience supporting HSE, Process Safety, industrial operations, construction safety, or major capital project delivery.
  • Professional certifications such as CSP, CIH, CHMM, ASP, PE, CCPSC, or equivalent preferred.
  • Minimum 10 years of leadership experience overseeing HSE programs on large industrial, manufacturing, chemical, pharmaceutical, energy, or infrastructure projects.
  • Demonstrated experience supporting programs exceeding $1 billion in capital value.
  • Pharmaceutical industry experience preferred; semiconductor, chemical processing, petrochemical, battery manufacturing, energy, advanced manufacturing, or other highly regulated industrial sectors will also be considered.
  • Experience leading incident investigations, root cause analysis programs, corrective action management, and assurance reviews.
  • Experience managing contractor HSE compliance and performance across multiple EPC organizations.
  • Experience performing HSE audits, management system assessments, and governance reviews.
  • Experience presenting HSE performance, risks, and recommendations to executive leadership teams.
  • Demonstrated experience implementing and governing Process Safety Management programs within complex industrial environments.
  • Demonstrated success working on large, fast-paced programs with multiple contractors and stakeholders.
  • Familiarity with GMP-regulated pharmaceutical manufacturing environments preferred.
  • Demonstrated ability to identify systemic risks and implement proactive mitigation strategies.
  • Extensive knowledge of OSHA regulations, Process Safety Management, contractor safety management, and industrial risk management practices.
  • Strong understanding of design, construction, commissioning, startup, and operational readiness activities from an HSE and PSM perspective.
  • Strong understanding of environmental regulatory compliance, permitting obligations, and sustainability considerations.
  • Strong analytical, organizational, and problem-solving capabilities.
  • Exceptional communication, leadership, stakeholder management, and influencing skills.
  • Full-time on-site engagement required.

Rewards & benefits
At AtkinsRéalis, our values-Safety, Integrity, Collaboration, Innovation, and Excellence-are more than just words. They are the foundation of who we are and how we work. These principles shape our culture, guide our decisions, and inspire us to create an environment where every team member feels empowered to grow, succeed, and make a meaningful impact.
Depending on your employment status, AtkinsRéalis benefits may include medical, dental, vision, company-paid life and short- and long-term disability benefits, employer-matched 401(k) with 100% vesting, employee stock purchase plan, Paid Time Off, leaves of absences options, flexible work options, recognition and employee satisfaction programs, employee assistance program, and voluntary benefits. You can review our comprehensive benefits page here.
About AtkinsRéalis
We're AtkinsRéalis, a world-class engineering services and nuclear organization. We connect people, data and technology to transform the world's infrastructure and energy systems. Together, with our industry partners and clients, and our global team of consultants, designers, engineers and project managers, we can change the world. We're committed to leading our clients across our various end markets to engineer a better future for our planet and its people.
Find out more.
Additional information
Expected compensation range is between $170,000 - $200,000+ annually depending on skills, experience, and geographical location.
Are you ready to expand your career with us? Apply today and help us shape something extraordinary.
AtkinsRéalis is an equal opportunity, Drug-Free employer EOE/Veteran/Disability
Please review AtkinsRéalis' Equal Opportunity Statement here.
AtkinsRéalis cares about your privacy and is committed to protecting your privacy. Please consult our Privacy Notice on our Careers site to know more about how we collect, use and transfer your Personal Data. By submitting your personal information to AtkinsRéalis, you confirm that you have read and accept our Privacy Notice.
Note to staffing and direct hire agencies:
In the event a recruiter or agency who is not on our preferred supplier list submits a resume/candidate to anyone in the company, AtkinsRéalis family of companies, we explicitly reserve the right to recruit and hire the candidate(s) at our discretion and without any financial obligation to the recruiter or agency. https://careers.atkinsrealis.com/recruitment-agencies
Worker Type
Employee
Job Type
Regular
At AtkinsRéalis, we seek to hire individuals with diverse characteristics, backgrounds and perspectives. We strongly believe that world-class talent makes no distinctions based on gender, ethnic or national origin, sexual identity and orientation, age, religion or disability, but enriches itself through these differences.