CQV HSE Advisor
Asset Recruitment View all jobs
- Limerick
- Contract
- Full-time
The CQV EHS Advisor will provide specialist Environmental, Health & Safety support during Commissioning, Qualification and Validation activities within a pharmaceutical manufacturing environment.Key Deliverables
- CQV EHS risk assessments and approvals
- Permit‑to‑Work oversight records
- EHS input to CQV readiness, handover and validation documentation
- Incident investigation reports and corrective action tracking
- Field safety inspection and SIMOPS reports
- Review and approve CQV‑specific risk assessments
- Oversee correct application of Permit‑to‑Work systems, including:
- LOTO and complex system isolation
- Confined space entry (tanks, vessels, HVAC plenums)
- Hot work in GMP and non‑GMP areas
- Support safe de‑isolation and re‑qualification activities during start‑up.
- Perform routine EHS inspections and safety walks in GMP and non‑GMP areas during CQV execution.
- Monitor contractor and vendor compliance with:
- Site EHS rules
- Intervene where unsafe practices may pose risk to personnel safety or product integrity.
- Site EHS induction
- GMP awareness training
- Task‑specific safety training (LOTO, chemicals, cleanroom behaviour)
- Deliver CQV‑focused toolbox talks addressing pharmaceutical‑specific hazards.
- Actively promote a strong safety and quality culture during high‑risk start‑up phases.
- CQV Engineers, Leads and Validation Teams
- Site EHS and Operational EHS
- Quality Assurance (QA)
- Operations and Manufacturing Science & Technology (MS&T)
- Construction Management
- Contractors, OEMs and Vendors
- Lead or support incident and near‑miss investigations related to CQV activities.
- Ensure documentation and corrective actions are inspection‑ready.
- Support regulatory inspections and internal audits related to start‑up, commissioning and validation phases.
- Maintain traceable records demonstrating EHS control during critical CQV activities.
- Degree/Diploma in EHS
- Relevant experience in a similar role