Brightwater – Limerick – This leading pharmaceutical and biotechnology company now has a role open for a Compliance Engineer responsible for ensuring cGMP compliance for the Tech Ops Engineering & Automation Department. Responsibilities * Acts as a liaison between Engineering & Automation and onsite quality and regulatory groups to define and address compliance related items. Identifies opportunities for continuous improvement of compliance and leads improvement initiatives. Provides support, information, and assistance to individuals, groups and management with the initiation, review, submission, and follow-up of documents such as Change Controls, EOE’s, NOE’s, DNF’s, risk assessments, impact statements and corrective/prevention action plans. Participates in investigations and root cause analysis for department issues of non-compliance. Provides periodic reviews of department documentation and records such as Periodic Evaluation Reports (PER), logbooks, preventative maintenance records/work orders, etc… – Permanent – Full-timeApply for this job.