- ResponsibilitiesReview and approve batch records for Cell Culture and Purification operations to ensure cGMP compliance.Assist with QA documentation management, issue resolution, and efficiency metrics.Support change management, deviations, CAPA systems, and batch release reviews.Help with site risk management and maintenance of the Electronic Quality Management System.Provide QA support to Quality Control, including reviewing raw data, non-conformance reResponsibilitiesReview and approve batch records for Cell Culture and Purification operations to ensure cGMP compliance.Assist with QA documentation management, issue resolution, and efficiency metrics.Support change management, deviations, CAPA systems, and batch release reviews.Help with site risk management and maintenance of the Electronic Quality Management System.Provide QA support to Quality Control, including reviewing raw data, non-conformance re
- Our client, a leading manufacturer of innovative medical devices, is seeking a highly skilled and motivated Maintenance Engineer to join their team. They are committed to providing a supportive and challenging work environment where you can contribute your expertise to the advancement of health-care technology.The salary for this role is 55k and it is a fully on-site, permanent position,Key Responsibilities:Delivers daily technical support to the operationOur client, a leading manufacturer of innovative medical devices, is seeking a highly skilled and motivated Maintenance Engineer to join their team. They are committed to providing a supportive and challenging work environment where you can contribute your expertise to the advancement of health-care technology.The salary for this role is 55k and it is a fully on-site, permanent position,Key Responsibilities:Delivers daily technical support to the operation
- Our Global Pharmaceuticals client is currently hiring for a Environmental, Health and Safety Specialist position. Responsible for the ongoing development of the EHS management system and it's component parts, (SOPs, Training documents and policies) to ensure regulatory and corporate compliance. Ensure compliance with applicable regulatory and corporate health and safety requirements in a manner consistent with continued plant profitability. This is a contrOur Global Pharmaceuticals client is currently hiring for a Environmental, Health and Safety Specialist position. Responsible for the ongoing development of the EHS management system and it's component parts, (SOPs, Training documents and policies) to ensure regulatory and corporate compliance. Ensure compliance with applicable regulatory and corporate health and safety requirements in a manner consistent with continued plant profitability. This is a contr
- Our large Logistics client is currently hiring for a Business Development position. You will be mainly responsible for developing the client's business within the new and existing business. This is a permanent position, based in Ireland on a hybrid basis. Key Responsibilities: Winning new business.Building partnerships with new and existing clients.Playing a key role in the entire sales cycle. Requirements Experience within logistics within BioPharma isOur large Logistics client is currently hiring for a Business Development position. You will be mainly responsible for developing the client's business within the new and existing business. This is a permanent position, based in Ireland on a hybrid basis. Key Responsibilities: Winning new business.Building partnerships with new and existing clients.Playing a key role in the entire sales cycle. Requirements Experience within logistics within BioPharma is
- Responsibilities:P.O. generation and ordering for manufacturing to support production batchesAssist with writing SOPs and Forms. Record data and log activities according to cGMP standards. Calibration, set-up and use of production equipment including - autoclave, balances, pH and conductivity meters, osmometers, Blood Gas Analyzers and peristaltic pumps.Prepare solutions, including buffers, reagents, and cell culture media and related tasks including butResponsibilities:P.O. generation and ordering for manufacturing to support production batchesAssist with writing SOPs and Forms. Record data and log activities according to cGMP standards. Calibration, set-up and use of production equipment including - autoclave, balances, pH and conductivity meters, osmometers, Blood Gas Analyzers and peristaltic pumps.Prepare solutions, including buffers, reagents, and cell culture media and related tasks including but
