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Initial Therapeutics, Inc. is seeking a Senior Director HSE to oversee health, safety, and environmental programs at the Concord Plant. This role involves ensuring compliance with regulations, developing HSE initiatives, and managing teams to support solid operational practices in a manufacturing setting.
The ideal candidate will have extensive experience in HSE leadership and a track record of interfacing with regulatory agencies. A Bachelor's degree and several years of leadership experience are required to foster a safe workplace environment.
Reports to the Concord Plant Site Head.
The Senior Director, HSE (Health, Safety, and Environmental), is directly responsible for the development, implementation, and maintenance of the HSE programs and systems for the Concord Plant manufacturing site. The Senior Director HSE is responsible for the productivity and development of the HSE employees, resolution of health, safety and environmental issues and ensuring compliance to Corporate and regulatory requirements.
This role provides HSE oversight for all site operations, including Manufacturing, environmental control, utilities, and waste operations, lab facilities, emergency response, and administrative facilities.
In addition, the Senior Director HSE provides functional HSE leadership, direction and governance to the HSE organization at the site. This role will connect the Concord Plant HSE team to the Corporate HSE group to ensure alignment and will be responsible for the systems that support regulatory inspections. The Senior Director HSE is a member of the Concord Plant Site Lead Team. The Lead Team has collective responsibility to develop and implement the strategic direction, organizational capability and management of the site. Primarily, the Lead Team drives the site toward achieving long term business objectives; continuously develops the business and organization for the future; and manages issues that span multiple teams in the organization and extend into the broader corporate/external context.
Site Lead Team members provide oversight to enable successful project delivery, build and empower a resilient organization, and implement the necessary systems and business processes required to support GMP operations, and progress the site culture. This requires significant collaboration, creativity and flexibility as the site undertakes full-scale GMP manufacturing operations.
The anticipated wage for this position is $156,000 - $228,800.
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.