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
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
Welcome to a different kind of role and a different kind of company. Ranked as one of Irelands best workplaces, by Great Place to Work, Harvey Norman, is a high-profile, leading-edge retail brand with over 289
Provide technical manufacturing support to Operations and Engineering. How Will You Make An Impact? Troubleshoot and recommend maintenance to limit downtime, to keep production on schedule, and to ensure ongoing validation compliance Design, set-up and execute
Within this role you will be responsible for designing, specifying and commissioning new and renovated biopharmaceutical process equipment. You will be providing engineering support and problem solving for existing equipment and manufacturing processes. As a Senior
Summary: This position is responsible for the receipt, documentation, and movement of inventory and non-inventory items within the plant and from outside sources. This position also performs labeling and shipping functions as needed. Essential Duties and
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
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
Within this role you will be responsible for certification of qualified equipment and systems e.g. cleanrooms and HEPA systems, in accordance with Standard Operating Procedures (SOPs), cGMPs and regulatory requirements. As a Facilities Cleanroom & HEPA
Main Location - Newcastle West Summary: Reporting to the Health and Safety Manager this is an exciting opportunity to develop in a role that will be expected to perform all tasks associated with developing and implementing
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
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 responsible for providing engineering support, troubleshooting, & subject matter expertise to the Facilities Operations, Utilities & HVAC teams. Designs, specifies & commissions new and renovated biopharmaceutical utilities & HVAC equipment,
Within this role you will be responsible for designing, specifying and commissioning new and renovated biopharmaceutical process equipment. Providing engineering support and problem solving for existing equipment and manufacturing processes. As a Principal Project Engineer, 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. As a
Within this role you will be responsible for all aspects of the assigned QA Team; provide leadership and support to direct reports; provides QA oversight to ensure that drug substance manufacturing activities are compliant with Quality
This position provides on the floor leadership to a team responsible for the receipt, documentation, and movement of inventory and non-inventory items within the plant and from outside sources. This position also performs labeling and shipping
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
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
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