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Regeneron Ireland

Regeneron Ireland

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.

In Ireland, Regeneron have a corporate office based in Harcourt Street, Dublin and are currently building a world-class biopharmaceutical production facility in the Raheen Business Park, Limerick.

This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron’s unwavering commitment to turn science into medicine.

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Overall rating
5
Based on 5 employee reviews
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4
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Regeneron Ireland Jobs
(27)

Supervisor Biotech Production

  • See description
  • Updated 19/10/2017
  • Limerick

Summary: Supervises the implementation of the manufacturing production schedules. Supervises the manufacturing team in relation to process execution for Upstream/Midstream and Downstream processes.

Site Quality Lead, DirectorSenior Director

  • See description
  • Updated 18/10/2017
  • Limerick

Summary: The successful candidate will be responsible for the development and execution of the strategy and plan for the Industrial Operations and Product Supply (IOPS) quality function.

Project Manager, Technology Transfer

  • See description
  • Updated 18/10/2017
  • Limerick

Summary: Based at the Raheen, Limerick site, the Project Manager will work with the Manufacturing Sciences and Technology (MSAT) group in Rensselaer, New York to transfer manufacturing processes to Raheen and partner facilities.

IT Analyst

  • See description
  • Updated 18/10/2017
  • Limerick

The IT Systems Generalist is responsible for the day to day maintenance, business & technical support and enhancements of the G&A (General & Administrative) applications.

Principal QA Validation Specialist - Cleaning

  • See description
  • Updated 18/10/2017
  • Limerick

Validate/qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures

Automation Engineer

  • See description
  • Updated 17/10/2017
  • Limerick

Summary: Regeneron has a requirement for an Automation Engineer for the startup, commissioning and sustaining of a pharmaceutical manufacturing facility in Raheen.

Downstream Process Specialist

  • See description
  • Updated 17/10/2017
  • Limerick

Summary: Provides on the floor direction to the manufacturing process. Key member in the implementation of large scale commercial manufacturing production program.

Sr IT Business Analyst

  • See description
  • Updated 17/10/2017
  • Limerick

Summary: Responsible for understanding complex business processes, eliciting and documenting requirements and coordinating communication among various business groups and IT.

QA Associate

  • See description
  • Updated 17/10/2017
  • Limerick

Summary: Performs activities in support of dispositioning product and/or raw materials while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents.

Supervisor Manufacturing Compliance

  • See description
  • Updated 17/10/2017
  • Limerick

Summary: Supervises the commercial manufacturing compliance requirements. Supervises the compliance team in relation to completion of quality instances for the Manufacturing departments.

QC Scientist

  • See description
  • Updated 17/10/2017
  • Limerick

Perform assay development, characterization, optimization, transfer, validation and investigation for QC chemistry group. Provide technical support, guidance and supervision for release, stability, and in-process testing and assay development.

Quality Compliance Specialist

  • See description
  • Updated 17/10/2017
  • Limerick

Maintains site compliance of operations inclusive of but not limited to Manufacturing, Quality Systems, QC, QA, Facilities Maintenance, Materials Handling, and QA Validation in accordance with mandated regulatory requirements and site expectations.

IT Analyst - Learning Mgt System

  • See description
  • Updated 17/10/2017
  • Limerick

Configures the Compliance Wire software to meet end-user needs. Processes system change control, documents configuration and writes test plans.

IT MES Analyst

  • See description
  • Updated 17/10/2017
  • Limerick

Responsible for the overall system maintenance and on-going support of the MES including change controls, documents and maintains configurations to ensure a validated state. Provides MES configuration and support services to meet end-user needs.

Process Analytics IT Analyst

  • See description
  • Updated 17/10/2017
  • Limerick

Summary: The Process Analytics IT Analyst will be responsible for the implementation and subsequent day to day support and administration of existing and future Business and Process Intelligence systems (currently Discoverant) in Raheen, Limerick.

Sr Mgr Process Sciences - Downstream

  • See description
  • Updated 16/10/2017
  • Limerick

Snr Manager - Process Sciences, Downstream, will be responsible for leading and developing a team of Purification Senior Scientists, Scientists and Associates that perform laboratory studies related to the production processes for biological drugs.

Computer System Validation Engineer

  • See description
  • Updated 16/10/2017
  • Limerick

The individual in this position implements policies and procedures to validate/qualify production automation/enterprise systems.

MgrSr. Mgr CMC Regulatory Sciences

  • See description
  • Updated 14/10/2017
  • Limerick

Responsible for overseeing information collection, distillation and assessment activities associated with the support functions and preparation of regulatory submissions and Product Quality Reviews, as required.

Sr Process Scientist - Purification

  • See description
  • Updated 14/10/2017
  • Limerick

Supports the Process Sciences Department through small scale laboratory experiments, as well as analysis, troubleshooting, and validation of manufacturing bioprocesses.

QA Validation Specialist - QC

  • See description
  • Updated 14/10/2017
  • Limerick

Implements policies and procedures to validate/qualify equipment, systems, and processes in accordance with regulatory requirements and company manufacturing standards.

MSAT Specialist

  • See description
  • Updated 14/10/2017
  • Limerick

Provide technical support for internal and external technology transfer of biopharmaceutical drug substance manufacturing processes for monoclonal antibodies/therapeutic proteins and provide post transfer support.

Sr Manager Quality Risk management

  • See description
  • Updated 14/10/2017
  • Limerick

Responsible for providing professional expertise and leadership in the Quality Risk Management function on a global scale.

Mger Sr Mger, Global Clinical Feasability

The Manager, Global Feasability will utilize high quality operational plans, recruitment plans and feasibility data to help optimize Clinical Study Concepts.

Upstream Process Specialist

  • See description
  • Updated 13/10/2017
  • Limerick

Summary: Provides on the floor direction to the manufacturing teams. Key member in the implementation of large scale commercial manufacturing production program.

QC Microbiology Analyst

  • See description
  • Updated 12/10/2017
  • Limerick

Summary: Perform a wide variety of microbial testing to support raw material, utilities, in-process and bulk drug substance manufacture in a cGMP regulatory environment.

Senior Compliance Specialist

  • See description
  • Updated 12/10/2017
  • Limerick

Summary: The position coordinates cGMP compliance for the Raheen Facilities Department.

Lead Materials & Dispensing Technician

  • See description
  • Updated 12/10/2017
  • Limerick

Summary: Lead is responsible for performing leadership-related activities with their direct reports and performs all tasks necessary within the Materials & Dispensing Technician role to support IOPS manufacturing operations.

Regeneron reviews
(5)

Happy employee

Anonymous in Dublin, Ireland
current employee in N 2017
14/05/2017

The Best Bits

Dynamic, fun, science driven, fast paced , interesting, great opportunities

Things to improve

Genuinely nothing I really want to change. It is a great place

Report

Please describe the problem with this review.

Challenging, rewarding and most importantly, getting the balance right.

Anonymous in Limerick, Ireland
former employee in 2016
26/04/2017

The Best Bits

The challenges and environment of the workplace - great to work for a company who are producing valuable biopharm products for patients.

Things to improve

Every day is a continuous improvement within the company as employees are being proactive.

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Please describe the problem with this review.

review

Anonymous in Limerick, Ireland
current employee in H 2016
18/07/2016

The Best Bits

Good perks,

Things to improve

start-up so demanding and no flexi time in place

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Please describe the problem with this review.

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