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
Within this role you will perform a wide variety of chemical or biological analyses on, products, in-process materials, or stability samples in support of the companys quality program. As a QC Analyst within the HPLC Lab,
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 Temp QC
Process Sciences is a technical services department that deals with a range of scientific, technical, engineering and mathematical needs from the laboratory to the manufacturing floor. Process Sciences is made of six main functional teams namely: (1) Upstream
Analog Devices, Inc. (NASDAQ: ADI) is a global semiconductor leader that bridges the physical and digital worlds to enable breakthroughs at the Intelligent Edge. ADI combines analog, digital, and software technologies into solutions that help drive
Job Description: SSE a CWS group company with over 20 years experience is an award winning company that specialises in Cleanroom services, contract cleaning, facilities services and facilities audits. At SSE we operate within the Life
Within this role you will be responsible for the development of analytic solutions that support Industrial Operations and Product Supply (IOPS). The analyst will work with the business to deliver analytic solutions that change the way
Within this role you will be responsible for the management and leadership of the Technical Operations Quality & Compliance function, providing quality and compliance oversight and support to the Facilities, Engineering and Automation departments under the
Within this role you will be responsible for the management and leadership of the Technical Operations Quality & Compliance function, providing quality and compliance oversight and support to the Facilities, Engineering and Automation departments under the
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
As a Compliance Analyst you will support the QC organization in meeting compliance targets through laboratory investigation and deviation management. The Compliance Analyst will report quality system metrics to the group and identify improvements that can
SSE a CWS group company with over 20 years experience is an award winning company that specialises in Cleanroom services, contract cleaning, facilities services and facilities audits. At SSE we operate within the Life Sciences Sectors, providing
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 culture
Within this role you will be responsible fordesigning, building and maintaining digital infrastructure platforms to drive innovation by making informed decisions using real-time data and information. As a Senior Automation Infrastructure Engineer, a typical day might include,
Summary of role: Please Note Person must be based in IRELAND! We are seeking a Lead Data Engineer with extensive big data frameworks expertise to join our team. The ideal candidate will have a strong background using Amazon
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 frame
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 Specialist
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
Within this role you will lead the Global Laboratory Systems team within the Information Technology function and will be responsible for managing the system lifecycle development, maintenance and compliance activities for laboratory software and process control