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 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,
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 perform a variety of chemical or biological analyses on raw materials, products, in-process materials, or stability samples in support of the companys quality program. As a QC Analyst within the Biochemistry
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 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 trends,
Within this role you will bebresponsible for ensuring that the IOPS IT group is operating in compliance with Regulatory requirements and Regeneron internal procedures as well being the key liaison between the IT and Quality Assurance
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
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
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,
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 the management and oversight of the QA Operations, Document Control (DC) function. This role will be part of the QA Operations site management team. This role includes oversight of the
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
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
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
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
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