Manager, EHS

Overview As the site EH&S leader at the Canton vaccine drug substance site, you own and advance all EH&S programs across start-up, ramp-up, and steady-state GMP operations. You ensure regulatory readiness and GMP compliance, partnering with cross-functional teams and regulators to foster a proactive safety culture. You will lead risk assessments, incident investigations, and performance metrics while aligning site practices with enterprise standards. This role offers meaningful impact through safeguarding people, processes, and the mission of delivering safe vaccines. Compensation / Benefitscomprehensive benefits packagebase salary with potential incentive compensationannual bonuslong-term incentives (stock options)competitive pay rangecareer development opportunities ResponsibilitiesLead as the site EH&S single point of accountability across start-up to steady-state GMP operationsDevelop, implement, and continuously improve EH&S programs, policies, and procedures for GMP environmentsMaintain compliance with OSHA, EPA, MassDEP, and other regulatory bodies; own permits, licenses, and reportingAct as primary liaison with regulators and auditors; lead inspections and responsesSupport site start-up activities including facility readiness, commissioning, qualification, and risk assessmentsConduct EH&S risk assessments (JSA, PHA, biosafety) to identify and mitigate risksManage incident investigations, root cause analysis, and CAPA closuresEstablish EH&S performance metrics; provide data-driven insights to site leadershipDevelop environmental compliance programs (hazardous waste, wastewater, air, stormwater, chemical inventories)Oversee occupational health and industrial hygiene programs including medical surveillance and exposure monitoringLead contractor safety and permit-to-work programs for construction and maintenanceReview and approve SOPs, change controls, deviations, and capital projects for EH&S risk controlPromote EH&S engagement, training, and leadership visibility across the organizationCollaborate with corporate EH&S to align with enterprise standards and regulatory expectationsServe as responsible or alternate official for biosafety, biosecurity, and select agent programs where applicable Key requirementsEight+ years of progressive EH&S experience in a regulated manufacturing environmentStrong experience in cGMP pharmaceutical, vaccine, biologics, or biotechnology manufacturing operations including start-up or commissioningDeep knowledge of OSHA, EPA, and MassDEP (experience preferred) regulationsTrack record in leading EH&S inspections and audits with effective corrective actionsExperience managing EH&S risks in biologics or vaccine environments (biosafety, chemical hazards, high-containment)Working knowledge of EH&S management systems (ISO 14001, ISO 45001) integrated with GMPAbility to operate independently as a site lead in a fast-paced settingExcellent communication and stakeholder management; able to engage senior leadership and regulatorsProfessional CSP, CIH, CHMM or equivalent strongly preferred or obtainable within defined timeframeStrong communication and influencing skillsStakeholder management at senior levelsProactive problem solving and decision makingRegulatory compliance mastery (OSHA, EPA, MassDEP)EH&S management systems (ISO 14001, ISO 45001)Biosafety and high-containment practices