EHS Specialist

Position Overview

An opportunity is available for a knowledgeable EHS Specialist to join a regulated manufacturing site in Ireland on a 12-month contract basis. The role involves ensuring adherence to Environmental, Health & Safety requirements within a medical device manufacturing context. Collaborating with operational, engineering, quality, and leadership groups, the Specialist will foster a culture of safety and contribute to continuous operational enhancements.

Key Duties and Responsibilities

• Manage daily EHS operations across the site
• Perform and evaluate risk assessments, establishing practical control measures
• Lead or assist with incident investigations, Root Cause Analysis, and oversee CAPA processes
• Support Process Safety Management initiatives within production activities
• Engage in HAZOP studies and drive risk mitigation efforts
• Conduct site inspections, audits, and safety walkthroughs
• Ensure compliance with internal protocols, relevant Irish legislation, and EHS standards
• Oversee contractor safety management alongside Permit-to-Work and high-risk job oversight
• Provide EHS training aimed at reinforcing a positive safety mindset
• Assist in ISO system compliance, corrective action tracking, and reporting
• Monitor EHS performance metrics and contribute to reporting obligations
• Work collaboratively with cross-functional teams including Operations, Engineering, Maintenance, and Quality

Required Qualifications and Skills

• Degree or diploma in Environmental Health & Safety, Engineering, Science, or related field
• Relevant EHS experience within Medical Device, Pharmaceutical, Diagnostics, Chemical, or other regulated manufacturing settings
• Demonstrated expertise conducting HAZOP studies and supporting Process Safety Management
• Proficiency in risk assessments, incident investigations, CAPA management, contractor oversight, Permit-to-Work systems, and safety audits/inspections
• Familiarity with ISO 14001 and ISO 45001 standards
• Strong communication and stakeholder engagement capabilities
• Capable of working autonomously and collaboratively within teams

Desirable Experience

• Experience within GMP-regulated manufacturing
• Exposure to HAZID, LOPA, PSSR, MOC, ATEX, COMAH, or SEVESO frameworks
• Background in environmental compliance and sustainability programs
• Knowledge of occupational health or industrial hygiene

Additional Information

• Must have actively participated in or led HAZOP studies
• Applicants must hold valid working rights in Ireland (e.g., Stamp 4, Stamp 1G, EU citizenship, or comparable unrestricted authorization)
• Onsite presence in Ireland is mandatory