Role OverviewThe Site HSE Manager is responsible for supporting the expansion of Durham campus operations to include Large Molecule drug substance production at our new facility in RTP, NC. This vital position will develop, implement, and track completion of HSE deliverables and needs.
What You Will Do
Lead the design and implementation of robust HSE programs and controls to ensure safe and compliant start-up of LMO production operations. Integrate LMO-specific HSE requirements into site-wide frameworks, including processes, systems, and training programs.
Why It Might Be a Fit
This role will be the Functional Lead for Occupational Safety programs across the Durham campus’s overall Gene Therapy/LMO/ADP operations. The role will lead implementation of robust HSE programs to ensure the protection of associated and the environment while simultaneously contributing to a strong, proactive, and enabling HSE culture.
Requirements
- 8+ years of HSE program development/management experience in a manufacturing/laboratory environment, preferably within the biopharmaceutical industry.
- Bachelor’s or Master’s degree in Occupational Health & Safety, Environmental Science, Engineering, Biology, or related field.
- Professional HSE certifications (e.g., CSP, CIH or equivalent) highly desired.
- Prior experience supporting the design and startup of new LMO/ADP facilities and manufacturing operations (e.g., PHAs, P&ID/design documentation review, HSE operational readiness) highly desired.
Benefits
- Comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits.
- Generous time off package including vacation, personal days, holidays and other leaves.
- Performance-based cash incentive.
- Annual equity awards (depending on the level of the role).
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