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Within this role you will be responsible for providing expertise and leadership in the quality function. You will be responsible to ensure that licensed product is certified and released to market in compliance with commercial manufacturing license and clinical (IMP) products. As an Associate Director Qualified Person a typical day might include ...

Company: Regeneron Ireland DAC (1 day ago)

The Associate Compliance Specialist-External Manufacturing is a member of the External Manufacturing Team and is responsible for operations support and compliance related activities for the manufacture of Regeneron products. This is a temporary 12-month contract position. A typical day might include, but is not limited to, the following: Leading ...

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

The Senior Accountant will be responsible for accounting for product sales (revenue recognition) by Regeneron's Ex-US entities, across Europe and Asia. A typical day might include, but is not limited to, the following: Completing revenue recognition activities and tasks on a monthly, quarterly and annual basis such as: Recording sales by legal ...

Company: Regeneron Ireland DAC (1 day ago)

The Senior QA Validation Specialist will validate/qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures. A typical day might include, but is not limited to, the following: Generating, executing and/or reviewing master and ...

Company: Regeneron Ireland DAC (6 days 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 (6 days 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 (6 days 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 (6 days 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 (5 days 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 (5 days 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 (5 days ago)

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 Associate Manager in QA Validation Oversight a typical day ...

Company: Regeneron Ireland DAC (4 days ago)

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 support the following areas; Upstream Sciences, Downstream Sciences, Analytical Technologies, IPC lifecycle, Data Analytics, Manufacturing Support, ...

Company: Regeneron Ireland DAC (4 days ago)

The Quality System Specialist participates 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 accordance with mandated regulatory requirements and site expectations. The Quality ...

Company: Regeneron Ireland DAC (4 days 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 (4 days 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 (3 days ago)

The successful candidate will be responsible for the management and leadership of the Quality Systems Operation function. As part of the QA Operations Site Management Team you will be a key leader in the cross functional support of cGMP compliance activities and will be immersed in Quality Systems for the site to identify potential risks and trends ...

Company: Regeneron Ireland DAC (3 days ago)

Within this role you will be responsible for the configuration, implementation, maintenance, and ongoing support of various IT applications and systems. As a Senior 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 (3 days ago)

Within this role you will be responsible for a broad variety of tasks to support the Irish payroll team in the completion of our bi-weekly and monthly payrolls. You will plan, prioritise and organise your workload and compile and record the Company's payroll and benefit data changes such as tax information. You will monitor changes to employee's ...

Company: Regeneron Ireland DAC Job type: temporary (3 days 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, a typical day might include, but is not limited to, the following: Coordinating across business departments and stakeholders, gathering, and implementing requirements ...

Company: Regeneron Ireland DAC (2 days ago)

As a QC Staff Scientist in Biochemistry you would participate in assay development, transfer, and validation for QC. You would provide technical support, guidance and supervision for release, stability, and in-process testing and assay development/validation and/or transfer. In this role a typical day might include, but is not limited to, the ...

Company: Regeneron Ireland DAC (2 days ago)