Within this role you will collaborate with the team to ensure business objectives are met through effective support of Drug Product manufacturing activities. Your remit will include organizing and driving critical Drug Product Manufacturing requirements to
About the job: CourseCo is an Irish Tech Company, supporting over 50,000 learners using our platform globally. We are small sized 10-20 team and provide a platform for businesses across Ireland UK to manage their booking,
The QC Compliance Specialist will be responsible for managing QCs Change Controls/CAPAs and Workflows. In this role a typical day might include, but is not limited to, the following: Coordination and documentation of QC quality records including
Within this role you will coordinate and priorities electronic laboratory data systems projects to maintain harmonization and electronic data integrity across IOPS sites and compliance with regulatory guidelines. This is a 12-month temporary contract. As a
Come join Analog Devices (ADI) – a place where Innovation meets Impact. For more than 55 years, Analog Devices has been inventing new breakthrough technologies that transform lives. At ADI you will work alongside the brightest
In this role you will be responsible for providing QA oversight and support to manufacturing activities. Performs and leads activities in support of dispositioning product while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs,
Within this role you will be using project management techniques and experience, the Project Specialist leads well-defined Quality Control projects. The Project Specialist may additionally support, plan and coordinate operational tasks for other QC projects under the guidance
We are currently looking to fill a Quality Compliance Specialist (Change Control)position on the Quality Assurance Change Control Team. This role works within the QA Change Control Team to primarily facilitate activities and relationships regarding change controls
Within this role you will be responsible for coordination and completion of manufacturing deviations and change controls. As an Associate / Compliance Specialist a typical day might include, but is not limited to, the following: Coordinating and
Within this role you will be responsible for leading the deployment and support of the Manufacturing Execution Systems (MES), Manufacturing Batch Records (MBRs), Generic Manufacturing Batch Records (GMBRs) and Equipment data. As a Manufacturing MES Specialist a
CNMII - Spine Liaison Nurse Specialist Part time - 0.5 FTE We are seeking to recruit a highly motivated Spine Liaison Nurse to join our Spine Excellence Centre located in Limerick. Role Summary To hold a key
Responsible for implementing microbiologically based initiatives as part of the QA Microbiology team at IOPS Raheen. Aspects of investigation activities, training, project implementation, and data collection and analysis will be utilized. Knowledge of Biopharmaceuticals and cell
Within this role you will be working as part of the Manufacturing team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors. As an Associate Biotech Production Specialist, a
In this role you will perform all compliance related tasks necessary to complete investigations and implementation of robust corrective actions for supporting manufacturing and site operations. Provide compliance expertise throughout the Engineering, Automation & Facilities departments.
Within this role you will be responsible for providing technical leadership and guidance for qualification activities and data integrity initiatives in regard to small manufacturing and laboratory equipment (e.g. HPLC/UPLC, TOC analyser, FTIR, microscopes) in the
Within this role you will be responsible for providing QA oversight and support to manufacturing activities. Performing and leading activities in support of dispositioning product while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs,
Within this role you will be responsible for leading the deployment and support of the Manufacturing Execution Systems (MES), Manufacturing Batch Records (MBRs), Generic Manufacturing Batch Records (GMBRs) and Equipment data. As a Senior Manufacturing MES
As a Quality Systems Specialist you will participate in maintaining site compliance of operations inclusive of but not limited to Manufacturing, Quality Systems, Quality Control, Quality Assurance, Facilities Maintenance, Engineering, Materials Handling, and QA Validation in accordance
Validate/qualify cleaning processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures A typical day as a QA Validation Specialist, may include: Generates, executes and/or reviews master and completed cleaning
Within this role you will be responsible for supporting the Environmental, Health and Safety for the Limerick IOPS location. As an EHS Specialist a typical day might include, but is not limited to, the following: Developing, implementing