Packaging BioProcess Specialist – Shanbally, Ringaskiddy, Cork
Onsite Role 2 Shift
Closing date: Tuesday 9th June 2026
Key Responsibilities
Support and partner closely with peer groups to ensure master batch records, SOPs, training records and other documents are current and compliant under cGMP conditions – ensure manufacturing systems and practices are consistent throughout the organization.
Own, investigate, write and approve associated deviations as well as support & coach Packaging Technicians in these functions – ensure adoption of ‘zero late’ mentality in meeting timelines.
Ensure areas meet compliance standards and audit areas against standards – highlight any issues and work proactively with the area team and others to ensure resolution.
Develop and demonstrate an active approach to safety, industrial hygiene, environmental and regulatory compliance.
Partner with validation subject matter experts, prepare/approve validation protocols, validation plans, protocol executions, and summary reports in support of ongoing revalidation and validation efforts required for commercial manufacturing.
Participate in cross‑functional teams, as applicable, to troubleshoot and resolve technical issues using root cause analysis tools.
Develop, define scope and support the implementation of technical solutions under the guidance of site change control systems.
Perform desk‑based tasks as required. For example, MES exception closure, deviation investigation or other administrative tasks.
Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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