- 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 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
- 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
- Responsibilities:Stay updated on ISO and FDA requirements to ensure audit readiness.Oversee Quality Operations, maintaining compliance with QMS and customer requirements.Lead and support QMS investigations, reviewing and approving reports promptly.Participate in and lead external audits and inspections as needed.Ensure compliance with customer quality requirements, including complaints and feedback oversight.Maintain Quality Metric Logs for Quality OperatiResponsibilities:Stay updated on ISO and FDA requirements to ensure audit readiness.Oversee Quality Operations, maintaining compliance with QMS and customer requirements.Lead and support QMS investigations, reviewing and approving reports promptly.Participate in and lead external audits and inspections as needed.Ensure compliance with customer quality requirements, including complaints and feedback oversight.Maintain Quality Metric Logs for Quality Operati
