Associate Director
Resilience
Associate Director
Resilience
Biologics and sterile injectables CDMO
A career at Resilience is more than just a job – it’s an opportunity to change the future.
Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.
For more information, please visit www.resilience.com
The Associate Director, EHS (Environment, Health, & Safety) & Security is a site EHS and Security leader responsible for sustaining a proactive, engaged safety and environmental culture across the West Chester and Blue Ash Sites. This role provides operational leadership and day-to-day oversight for EHS and physical security programs, ensuring regulatory compliance while driving continuous improvement, risk reduction, and employee ownership of safety.
The Associate Director partners closely with Operations, Engineering, Planning, Legal, Human Resources and Corporate EHS/Security to implement scalable systems that protect employees, the environment, and the business, while enabling operational excellence and growth.
Leadership & Culture
Strategy, Risk & Compliance
Operational Excellence & Continuous Improvement
Financial & Resource Accountability
Incident Management & Assurance
External Engagement & Reporting
Governance & Ethics
Minimum Qualifications
Preferred Qualifications
This role is based primarily in an office setting but requires regular presence on the manufacturing floor, including the ability to gown into controlled/cleanroom areas and wear personal protective equipment (PPE) as required, occasionally lift up to 20 lbs., and present or communicate effectively in both office and group settings.
Sponsorship or support for work authorization, including visas, is not available for this position.
Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.
Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, paid vacation, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $137,500.00 - $203,125.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience? We encourage you to apply and start a conversation with one of our recruiters.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.
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