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
As a QC Lab Instrumentation Analyst you would support the Quality Control (QC) and Process Sciences (PS) departments by maintaining their laboratory instrumentation in an operational, qualified state. This entails ensuring both instrument hardware and software qualifications
Within this role you will be responsible for enabling chemistry manufacturing and controls (CMC) quality and compliance excellence by ensuring Regeneron IOPS maintains effective systems for monitoring, analyzing, presenting, implementing, and influencing global regulatory and industry
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 Sciences Sectors,
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 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
Within this role you will be a vital part of a team focused primarily on the implementation and support of Waters Empower Chromatography (CDS) software in a highly regulated cGMP laboratory environment. The systems we support
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
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 Cleanroom
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
Summary: This role is responsible for the operational oversite of the QA Microbiology and Lab Support Teams at the Raheen site. This person is the leader for these two organizations and must ensure personnel management (goals,
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,
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 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
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
This position implements policies and procedures to review and approve validation/qualification documentation for equipment, systems, and processes in accordance with regulatory requirements and company manufacturing standards, and oversees a team of Validation Oversight Specialists. As an