Position: Pharmaceutical Production Operator Duration: 6 months, with the possibility of extension based on performance and
operational needs. Location: Dundalk, Ireland (on-site) Shift: Site operates on a 24/5 Monday to Friday and 6am – 6pm Saturday and
Sunday. Candidates must be willing to work all shifts patterns. Responsibilities:- Perform Oral Solid Dose filling line setup,
operation, line clearance, reconciliation, and cleaning processes.- Ensure all manufacturing operations adhere to standard
operating procedures, batch records and Good Manufacturing Practices.- Maintain accurate records in room logs, cleaning
logs, equipment logs, batch records, reconciliation logs.- Ensure that training file is complete and up to
date. - Complete line inspections and batch record to maintain
compliance with regulatory standards.- Provide input in the investigation of deviations, support
implementing corrective and preventive actions (CAPAs) to ensure timely
resolution, mitigate risks and prevent recurrence.- Support implementation of change controls,
ensuring seamless integration of changes with minimal impact on production.- Identify non-compliances to Line Leader and
Supervisor for investigation.- Complete training sessions for to reinforce best
practices, compliance, and efficiency in operations.- Collaborate with a team committed to efficiency
and teamwork, contributing to reduced downtime, increased throughput, and the
maintenance of high-quality standards.RequirementsRequirements:- If no BSc/MSc/PhD qualification - Minimum of 2
years of experience in the pharmaceutical industry, with a focus on
manufacturing operations, particularly OSD production.- If BSc/MSc/PhD qualification – graduates accepted
with 1 year necessary technical and cGMP knowledge.- Knowledge of cGMP requirements.- Fluent in English, with strong communication
skills to effectively learn, complete batch records and convey critical
information to supervisors.- Demonstrated ability to oversee manufacturing
processes, from setup and cleaning to changeover and compliance checks.BenefitsBenefits:- Gain valuable pharmaceutical industry experience.- Opportunity to work within a team that values
efficiency, teamwork, and the professional development of its members.- Engage in a role that directly contributes to
enhancing operational efficiencies, ensuring compliance, and maintaining
high-quality standards.