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Resilience

Biologics and sterile injectables CDMO

Associate Director - Environment, Health, and Safety, Security

Environmental Health & SafetyConfirmed live in the last 24 hours
Full-timeWest Chester Township, OH, USA

About the Job

Requirements

  • Demonstrated EHS work experience with a primary focus in Health, Safety, and Industrial Hygiene programs.
  • Working knowledge of local, state, and federal regulations and standards including the Occupational Safety and Health Administration, Environmental Protection Agency, Department of Transportation, National Fire Protection Association, and American National Standards Institute.
  • Demonstrated experience applying EHS management systems.
  • Excellent verbal and written communication skills, including technical writing.
  • Demonstrated ability to plan and implement complex programs and processes, and to drive change that delivers measurable results.
  • Business acumen and demonstrated ability to build and lead cross-functional teams.
  • Solid understanding of risk management as it relates to EHS and loss control.
  • Proficiency with Microsoft Office Suite and EHS management information systems.
  • The role requires regular presence on the manufacturing floor, the ability to gown into controlled or cleanroom areas and wear personal protective equipment, occasional lifting up to 20 pounds, and effective presentation and communication in office and group settings.

Responsibilities

  • Provide visible, values-based leadership to foster a proactive EHS and security culture grounded in employee engagement, accountability, and continuous improvement.
  • Serve as a trusted advisor to site and functional leadership, influencing decisions through data, risk insight, and practical solutions.
  • Lead, staff, and develop the site EHS and Security organization, including third-party providers such as occupational health, fitness, and security services; own workforce planning and performance management in partnership with Human Resources and the Director, Process and Strategic Initiatives, building bench strength and succession depth.
  • Champion site safety governance structures and floor-level safety initiatives that encourage employee participation and ownership.
  • Support the Director, Process and Strategic Initiatives on EHS and security-related decisions and external commitments in their absence, as needed.
  • Exercise delegated authority from the Director, Process and Strategic Initiatives for defined areas of the site's EHS and Security program, deciding independently within that scope, including in ambiguous situations with medium-term (6–12 month) implications, while balancing cross-functional trade-offs and escalating enterprise- or site-level trade-offs to the Director.
  • Translate site and corporate EHS and security strategy into actionable plans, aligning resources to deliver strategic priorities.
  • Identify applicable environmental, health, safety, and security risks and ensure effective controls are designed, implemented, and sustained.
  • Ensure compliance with local, state, and federal regulations, corporate EHS policies, management systems, and applicable industry best practices, including cGMP, GAMP, ITIL, and PMI.
  • Act as the recognized subject matter authority for EHS and security within the site; shape standards, best practices, and operating models, contributing to enterprise or cross-site working groups as needed.
  • Drive continuous improvement initiatives to reduce injuries, incidents, environmental impact, waste, and costs while improving overall EHS system effectiveness.
  • Establish, track, and improve EHS performance metrics; hold the team accountable for achieving site goals and leading indicators.
  • Support site sustainability initiatives, including client-specific and corporate sustainability commitments.
  • Partner with Operations and Engineering to integrate EHS requirements into processes, equipment design, and capital projects.
  • Partner with the Director, Process and Strategic Initiatives on operating and capital budget planning for the EHS and Security program, including related equipment and facility investments with Operations and Engineering, and own delivery against the approved budget.
  • Oversee investigation of incidents and near-misses, ensuring robust root cause analysis and sustainable corrective and preventive actions.
  • Ensure workplace inspections, audits, and risk assessments are conducted effectively and result in meaningful improvements.
  • Support and lead internal, external, customer, and regulatory inspections, including FDA, EMEA, and third-party audits.
  • Manage work-related injuries and partner with Human Resources as appropriate, including workers' compensation.
  • Build and maintain professional relationships with regulatory agencies, customers, and other external stakeholders, and partner with EHSS leads at other Resilience sites to align practices.
  • Ensure timely and accurate submission of required EHS reports, permits, and regulatory filings.
  • Manage external consultants, including defining scopes of work and overseeing performance.
  • Conduct all activities in alignment with company values, the Code of Ethics, and supporting policies; ensure required training and reporting obligations are met.

Desired Qualifications

  • Bachelor's degree in Occupational Safety and Health (OSH).
  • 10 or more years of experience in EHS, including people leadership.
  • Experience in the pharmaceutical industry.
  • Experience working in a Lean environment.
  • Strong knowledge of good manufacturing practices (GMPs).
  • Professional certification such as Certified Safety Professional (CSP) or Certified Industrial Hygienist (CIH).

About the Company

Resilience

Biologics and sterile injectables CDMO

Resilience is a North American CDMO focused on biologics and sterile drug products. It provides end-to-end services from development through commercial production, including biologics development and drug substance manufacturing, aseptic fill/finish, device assembly, packaging, logistics, regulatory support, and tech transfer, all coordinated via a stage-gate process and a digital quality management system. It differentiates itself with North American-based, integrated biologics and sterile capabilities, a focus on sterile injectables and device assembly, and recent expansion into injectable pen devices for diabetes and obesity medicines. Its goal is to broaden access to complex medicines while protecting North American biopharma supply chains with dependable capacity and strong regulatory support from clinical development to commercial scale.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$3.2B
Headquarters
Blue Ash, OH
Founded
2020

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