Hiring: Site HSE Specialist Company: Novartis Location: Durham, NC Job Posted Time: 2026-09-10 10:21:06 About the job Experience: •5+ years of HSE program development/management experience in a manufacturing/laboratory environment (preferably within the biopharmaceutical industry). Strong technical knowlege across HSE disciplines. Required Skills: •Lead the implementation of robust HSE programs and controls to enable safe and compliant start-up of ADP production operations. •Integrate ADP-specific HSE requirements into site-wide systems, processes, and training frameworks. •Partner with external providers and internal teams to deliver world-class safety performance across construction and operations. •Drive Occupational Safety excellence by developing and continuously improving critical programs (e.g., Process Safety, Electrical Safety, Fire Protection, Emergency Response). •Collaborate cross-functionally to embed HSE practices that support reliable commercial production and research operations. •Provide expert HSE guidance for new equipment, processes, and technology transfers, ensuring safe and efficient implementation. •Lead HSE impact assessments and manage change to ensure compliance and risk mitigation across site operations. •Act as a trusted technical expert, leading complex investigations and ensuring effective root cause analysis and resolution. Qualifications: •BS degree or higher in Occupational Health & Safety, Chemical Engineering, or related field. •Professional HSE certifications (e.g., CSP, CIH) or desire to attain them is strongly preferred. •Prior experience supporting the design and startup of new ADP/LMO facilities and manufacturing operations (e.g., PHAs, P&ID/design documentation review, HSE operational readiness) highly desired. •Strong influencer with the ability to work effectively and build relationships across a matrixed organization. •Excellent communication and technical writing skills. •Outstanding interpersonal skills for collaboration, creativity in problem solving, and ability to plan/perform multiple tasks with high quality as part of a high-paced work environment. •Knowledge of cGMP manufacturing regulations and requirements in conjunction with the delivery of effective EHS programs. •The salary for this position is expected to range between $89,600.00 and $166,400.00 annually. •The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. •Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. Compensation: •Competitive benefits and rewards package Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!