activities to assist with the management thereof. Description Main purpose of the job: To assist with the Quality Control activities for clinical trials, assist with regulatory communications and adherence, and study standard operating procedures at all times Assist with the preparation and follow-up of external QC/QA/External monitoring findings in conjunction with Managers Report and track critical events and protocol QC/QA/External monitoring findings in conjunction with Managers Take ownership and accountability for tasks &
data generated from test results. Manage media inventory management ensuring lab needs are met. Perform and training of staff. Assist Operations with rollout/operation of SOP management. Perform sterility testing testing and assist with sterility testing training and test development. Perform microbiological testing and change controls. Reporting issues to the QC Manager Calibration and Validation of Equipment and test accountability and responsibility Head of department/ line manager: Accountable for ensuring that all employees reporting
data generated from test results. Manage media inventory management ensuring lab needs are met. Perform and training of staff. Assist Operations with rollout/operation of SOP management. Perform sterility testing testing and assist with sterility testing training and test development. Perform microbiological testing and change controls. Reporting issues to the QC Manager Calibration and Validation of Equipment and test accountability and responsibility Head of department/ line manager: Accountable for ensuring that all employees reporting
offer assistance. Bachelor's degree in Quality Management or Advanced Diploma in Quality Management or NFQ have a certificates of ISO 9001:2015 Quality Management System. Implementation of QMS and Internal Auditing
and Records are signed off.
Main purpose of the job:
for an experienced RA Associate / RA Officer to assist the RA team. You need one full year of RA Officer pharmaceutical company to apply. The role is to support and assist the Regulatory Affairs pharmacists with the day-to-day
for an experienced RA Associate / RA Officer to assist the RA team. You need one full year of RA Officer pharmaceutical company to apply. The role is to support and assist the Regulatory Affairs pharmacists with the day-to-day
Health & Safety Act, National Environmental Management Act and related Regulations Registered as per Company Health, Safety and Environmental Compliance. Manage all H&S requirements on site. Establish safety accidents and near-misses. Management of all IOD cases and liaising with FEM. Management of Sites HSE functions functions and job hazard analyses. Assist company subcontractors to comply with legislation standards. Audit
Health & Safety Act, National Environmental Management Act and related Regulations Registered as per Company Health, Safety and Environmental Compliance. Manage all H&S requirements on site. Establish safety accidents and near-misses. Management of all IOD cases and liaising with FEM. Management of Sites HSE functions functions and job hazard analyses. Assist company subcontractors to comply with legislation standards. Audit