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Within this role you will coordinate and prioritize electronic laboratory data systems projects to maintain harmonization and electronic data integrity across IOPS sites and compliance with regulatory guidelines. As a QC Electronic Data Management Analyst, a typical day might include, but is not limited to, the following: Working with cross- ...

Company: Regeneron Ireland DAC (1 day ago)

Within this role you will be responsible for delivering complex and strategic IT projects across Applications and Infrastructure for IOPS. job As a IT Project Manager a typical day might include, but is not limited to, the following: Providing project management and/or business analysis support for the development and implementation of assigned ...

Company: Regeneron Ireland DAC (1 day ago)

Within this role you will perform sample management and method transfer activities to external laboratories for a wide variety of microbial and analytical techniques to support raw material, utilities, in-process and bulk drug substance manufacture in a cGMP regulatory environment. As a Temp QC External Lab Coordinatora typical day might include ...

Company: Regeneron Ireland DAC Job type: temporary (1 day ago)

The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS ...

Company: Regeneron Ireland DAC (1 day ago)

The External Warehouse and Logistics function manages the third-party EU warehousing network to deliver an effective and compliant operation that supports Regeneron Ireland's current and future needs. Within this role the Senior Supply Logistics Analyst will ensure that the external warehouse network is established in compliance with appropriate ...

Company: Regeneron Ireland DAC (1 week ago)

Clinical Study Associate Manager (CSAM) role supports the Clinical Study Lead (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs). The balance of direct execution versus oversight of CROs deliverables will vary ...

Company: Regeneron Ireland DAC (1 week ago)

Within this role you will be responsible for working with cross-functional teams to drive activities that will ensure a state of continuous GMP compliance in Regeneron IOPS and to build inspection readiness capability across the organization. This role will help to build mechanisms within the business to educate on compliance awareness and ensure ...

Company: Regeneron Ireland DAC (1 week ago)

Are you a seasoned payroll professional with a passion for accuracy and efficiency? Do you thrive in a dynamic, fast-paced environment and have a knack for managing international payrolls? If so, Regeneron is looking for you. As an Associate Manager, you will play a crucial role in ensuring our payroll processes run smoothly and accurately across ...

Company: Regeneron Ireland DAC (1 week ago)

Within this role you will be responsible for the configuration, implementation, maintenance, and ongoing support of various IT applications and systems. As an IT Applications Analyst within Lab Systems, a typical day might include, but is not limited to, the following: Coordinating across business departments and stakeholders, gathering and ...

Company: Regeneron Ireland DAC (1 week ago)

Within this role as a Manufacturing coordinator (PA12) you will be responsible for all schedule related activities in the manufacturing area daily, liaising with the scheduling dept in Manufacturing and other impacted areas. In addition, the Scheduler/Coordinator plays a lead role in the planning of other key activities in the area so that there is ...

Company: Regeneron Ireland DAC (1 week ago)

Within this role you will support the Process Sciences laboratory operations by supporting adherence to site policies and procedures associated with but not limited to good documentation practices, data integrity considerations, equipment and vendor maintenance and PS study execution, recording and reporting. As a Compliance Specialist within ...

Company: Regeneron Ireland DAC (1 week ago)

Within this role you will be responsible to work within the QA Change Control Team to primarily facilitate activities and relationships regarding External Manufacturing change controls. As an Manager a typical day might include, but is not limited to, the following: Leading and managing direct reports, working to develop and oversee their ...

Company: Regeneron Ireland DAC (1 week ago)

The Project Engineer designs, specifies and commissions new and renovated biopharmaceutical process equipment. The successful candidate will provide engineering support and problem solving for existing equipment and manufacturing processes & provide technical expertise to engineering, automation, and related departments. A typical day might include ...

Company: Regeneron Ireland DAC (1 week ago)

This role is responsible for the administration, coordination and completion of tasks on our computerized maintenance management system (CMMS). This is to maintain the required cGMP state of the computerised maintenance management system for the Raheen Facility through strict adherence to Standard Operating Procedures (SOPs) and cGMP's. A typical ...

Company: Regeneron Ireland DAC (1 week ago)

As a QC 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 be made in all quality system inputs. A typical day might include, but is not limited to, ...

Company: Regeneron Ireland DAC (1 week ago)

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. This is an days position. As a Manufacturing MES Specialist a typical shift might include, but is not limited to, the ...

Company: Regeneron Ireland DAC (1 week ago)

Within this role you will be responsible to provide key technical support for internal and external technology transfer of biopharmaceutical drug substance manufacturing processes for monoclonal antibodies/therapeutic proteins and provide post transfer support. This is a 12-month temporary contract As a Temp MSAT Specialist, a typical day will ...

Company: Regeneron Ireland DAC Job type: temporary (1 week ago)

Within this role you will perform a wide variety of bioanalytical processes to support bulk drug substance manufacture in a cGMP regulatory environment. As a QC Analyst within the Bioassay Lab, a typical day might include, but is not limited to, the following: Ensuring that all work carried out is in compliance with current GMP, the required ...

Company: Regeneron Ireland DAC (1 week ago)

The Supply Operations Department facilitates batch disposition and order management activities to receive and fulfill product supply requirements in a timely fashion, thereby ensuring patients' needs are met. The Supply Operations Manager will use a data driven approach in working collaboratively with the department leads globally to identify and ...

Company: Regeneron Ireland DAC (1 week ago)

Summary: Responsible for the supporting the QC Critical Materials, QC Reference Standards and Procurement of all categories of laboratory Chemicals and Components Quality Control at the Limerick Manufacturing. Essential Duties and Responsibilities include, but are not limited to, the following: Supporting the daily purchasing of laboratory ...

Company: Regeneron Ireland DAC (1 week ago)