1 Laboratory Consultant jobs in Ireland
QC Lab Equipment Specialist
Dublin, Leinster
Life Science Recruitment Ltd
Posted today
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Job Description
QC Lab Equipment Specialist (CMMS Maximo) - Hybrid RK4540 12 Months Dublin Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. The Senior QC Associate will be responsible for planning, executing, and documenting the qualification, calibration, and routine maintenance of laboratory systems in a cGMP Quality Control environment. Oversee tracking and management of activities through CMMS Maximo, authors and approves validation life cycle documents for computer-related systems, ensures data integrity compliance, and executes approved protocols. Duties: Planning and conducting routine calibration, requalification and maintenance of laboratory equipment ensuring calibration and maintenance schedules are adhered to as per CMMS Maximo. Reviewing & filing of QC calibration & maintenance documentation. Planning, executing and documenting the qualification of new laboratory equipment in a cGMP regulated environment, including the writing of equipment validation protocols and associated summary reports. Conduct periodic reviews of instrument validation as part of validation life cycle. Alerting Quality Control Management in the event of equipment failing to meet calibration or qualification requirements and conducting impact assessments/investigations as required Scheduling and coordination of equipment repairs and maintenance with vendors/contractors, while minimizing level of down-time for lab equipment, and disruption to laboratory activities. Participation in technical project teams to act as a subject matter expert on instrument validation regulations and procedures. Where applicable, owns and project manages change controls and adherence to Change Control metrics Supporting and managing the addition of project components to CMMA Maximo Act as a key contributor and sponsor to Data Integrity Assessments for Lab systems Any other tasks/projects assigned as per mangers request Education and Experience : Bachelors degree in a Science related field is required. Minimum of 3 years of laboratory experience in a cGMP laboratory environment including exposure to analytical instrument validation and data integrity assessments. Detailed knowledge of the methodology, and instrumentation and analytical techniques used for biopharmaceutical testing. Understanding of current regulatory requirements for cGMP laboratory equipment validation and electronic record integrity. Demonstrated success in managing an equipment qualification or maintenance program advantageous. If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.
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