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Regeneron Ireland

Regeneron Ireland

regeneron

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
4.3
Based on 6 employee reviews
5
83%
4
0%
3
0%
2
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1
17%
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Regeneron Ireland Jobs
(49)

CMC Regulatory Sciences Specialist

  • See description
  • Updated 21/06/2018
  • Limerick

Responsible for researching all CMC aspects of clinical and/or commercial manufacturing and for summarizing the information and data as outlined in regulations and guidance (e.g., ICH guidelines) for CMC documents as required.

Manager QA Operations

  • See description
  • Updated 21/06/2018
  • Limerick

The Manager QA Operations provides QA oversight to ensure that drug substance manufacturing activities are compliant with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents.

QC Micro Analyst I-IV (Compliance)

  • See description
  • Updated 20/06/2018
  • Limerick

Summary: Performs testing to ensure cGMP compliance in the manufacturing facility. Responsible for assessing the microbiological quality of products, manufacturing equipment, manufacturing process areas, and facility utilities.

QC Scientist

  • See description
  • Updated 20/06/2018
  • 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.

Sr Cost Accountant

  • See description
  • Updated 19/06/2018
  • Limerick

Summary: The successful candidate will be responsible for the cost accounting activities for the manufacturing facility in Limerick.

Applications Analyst

  • See description
  • Updated 19/06/2018
  • Limerick

The IT Applications Analyst is responsible for the implementation, system maintenance and on-going support of various IT Applications.

Temp Warehouse Associate

  • See description
  • Updated 19/06/2018
  • Limerick

Summary: This position is responsible for the receipt, documentation, and movement of inventory and non-inventory items within the plant and from outside sources. This position also performs labeling and shipping functions as needed.

Supervisor QC Chemistry - (Shift)

  • See description
  • Updated 19/06/2018
  • Limerick

Summary: Oversees the laboratory quality control testing of in-process, stability, and final drug products.

Sr Process Scientist - Purification

  • See description
  • Updated 18/06/2018
  • Limerick

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

Qualified Person

  • See description
  • Updated 18/06/2018
  • Limerick

Act in the capacity of a Qualified Person in accordance with Annex 16, EudraLex, Volume 4 and directive 2001/83/EC to support disposition of Regeneron Products.

Sr Quality Specialist

  • See description
  • Updated 18/06/2018
  • Limerick

Performs and leads 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.

Sr Compliance Specialist - Process Sciences

  • See description
  • Updated 18/06/2018
  • Limerick

Supports the Process Validation and Manufacturing Support group within the Process Sciences department by providing oversight for all aspects of cGMP compliance.

Lead Warehouse Associate

  • See description
  • Updated 18/06/2018
  • Limerick

This position provides on the floor leadership to a team responsible for the receipt, documentation, and movement of inventory and non-inventory items within the plant and from outside sources.

Shift Supervisor - Cell Culture Lab

  • See description
  • Updated 18/06/2018
  • Limerick

Supervises the Process Sciences Lab Shift Team in conducting small scale laboratory studies as part of investigations or characterisation primarily of upstream unit operations.

Warehouse Associate

  • See description
  • Updated 18/06/2018
  • Limerick

This position is responsible for the receipt, documentation, and movement of inventory and non-inventory items within the plant and from outside sources. This position also performs labeling and shipping functions as needed.

Biotech Production Compliance Coordinator

  • See description
  • Updated 18/06/2018
  • Limerick

Summary: Performs all compliance related administrative tasks necessary for supporting commercial manufacturing operations.

Biotech Production Specialist

  • See description
  • Updated 18/06/2018
  • Limerick

Summary: Performs all tasks necessary for the manufacturing operations of both clinical and commercial manufacturing programs.

Supervisor Facilities Maintenance (Utilities)

  • See description
  • Updated 18/06/2018
  • Limerick

Summary: Primarily responsible for the direction, organization and supervision of all Utilities maintenance operations and functions; this position is responsible for assisting the Facilities Maintenance Manager.

Senior Materials Planner

  • See description
  • Updated 18/06/2018
  • Limerick

Summary: Functions as part of Materials Management/Supply Chain by determining resources needed to meet manufacturing production schedule. Participates in Supply Chain projects, and improvement initiatives.

Biotech Production Inventory Coordinator

  • See description
  • Updated 18/06/2018
  • Limerick

Summary: Monitors and maintains raw material inventory levels, production batches and production samples for Commercial Manufacturing.

Supervisor Biotech Production Dispensing

  • See description
  • Updated 18/06/2018
  • Limerick

Summary: Supervises manufacturing operations.

MSAT Specialist

  • See description
  • Updated 18/06/2018
  • Limerick

Summary: 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.

Graduate Manufacturing Systems Analyst

  • See description
  • Updated 18/06/2018
  • Limerick

Summary: Responsible for Designing and Developing Manufacturing Production systems in a highly regulated Biopharmaceutical environment.

Quality Compliance Specialist - QRM

  • See description
  • Updated 18/06/2018
  • Limerick

Role supports the work of Regeneron's Industrial Operations and Product Supply (IOPS) site through the use of quality risk management (QRM) principles and techniques. The scope may also include collaboration with other IOPS Sites, partners, CMOs.

Project Manager, Quality Assurance

  • See description
  • Updated 18/06/2018
  • Limerick

Support manufacturing activities at CMOs and partners by providing quality oversight. Accomplishes quality objectives by planning and evaluating project activities. The PM support may include operations and validation.

Project Manager, Technology Transfer

  • See description
  • Updated 18/06/2018
  • Limerick

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.

Mgr/Sr Mgr CMC Program Management

  • See description
  • Updated 18/06/2018
  • Limerick

The Manager/Senior Manager uses extensive program management knowledge within the drug development industry to lead programs of advanced complexity and large scope, such as late stage clinical development or commercial.

Assoc. Director/Director, CMC Regulatory Affairs

  • See description
  • Updated 17/06/2018
  • Limerick

Regeneron offers a unique, world-class opportunity for interested candidates. Regeneron has been consistently ranked a "Top Employer" in Science Magazine's rankings for pharmaceutical and biotechnology companies.

Learning Management System Owner/Administrator

  • See description
  • Updated 16/06/2018
  • Limerick

This position is responsible for the Learning Management System (LMS), it's management and Training documentation. They perform a variety of complex tasks under general guidance and in compliance with cGMPs.

Temp - QC Microbiology Analyst (Compliance)

  • See description
  • Updated 15/06/2018
  • Limerick

Summary: Performs testing to ensure cGMP compliance in the manufacturing facility. Responsible for assessing the microbiological quality of products, manufacturing equipment, manufacturing process areas, and facility utilities.

Lead Maintenance Technician (Shift 24/7)

  • See description
  • Updated 15/06/2018
  • Limerick

Summary: Oversees the operations of the General Facilities, Process and Utilities area maintenance functions at the IOPS Ireland Manufacturing Plant.

Principle Automation Engineer

  • See description
  • Updated 15/06/2018
  • Limerick

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

Associate Lab Systems Analyst

  • See description
  • Updated 15/06/2018
  • Limerick

The Laboratory Systems Analyst will be a customer facing individual responsible for implementation and subsequent day to day support and maintenance of general Laboratory Computers systems.

Senior Microbiologist - Micro Support

  • See description
  • Updated 15/06/2018
  • Limerick

Summary: Responsible for QC microbiological aspects of cGMP compliance and testing ensuring microbiological quality of products, manufacturing equipment, manufacturing process areas, and facility/utilities.

MES Operations Analyst

  • See description
  • Updated 15/06/2018
  • Limerick

Summary: Responsible for the Design and Configuration of the Manufacturing Execution Systems (MES) manufacturing Batch Records and Equipment data.

Snr Project Engineer

  • See description
  • Updated 15/06/2018
  • Limerick

Summary: Designs, specifies and commissions new and renovated biopharmaceutical process equipment. Provides engineering support and problem solving for existing equipment and manufacturing processes.

Temp QC External Laboratory Coordinator

  • See description
  • Updated 15/06/2018
  • Limerick

Coordinate sample management and method transfer activities to external laboratories in a cGMP regulatory environment. Trending of reference standard/product data for in house and contract laboratories.

Mgr / Sr Mgr QC Microbiology

  • See description
  • Updated 15/06/2018
  • Limerick

Summary: The successful candidate will be responsible for the management of a team of Supervisors and analysts within the QC Microbiology department for a cGMP biopharmaceutical manufacturing facility.

Temporary Document Coordinator

  • See description
  • Updated 15/06/2018
  • Limerick

Provides support to the Raheen IOPS site related to documentation systems and ancillary support systems.

Manager QC Bioanalytics

  • See description
  • Updated 14/06/2018
  • Limerick

Summary: Oversees the laboratory quality control testing of in-process, stability, and final drug products. Has technical responsibility for all bioanalytical aspects of QC testing.

QC Analyst Biochemistry

  • See description
  • Updated 14/06/2018
  • Limerick

Summary: Perform a wide variety of bioanalytical processes to support in-process and bulk drug substance manufacture in a cGMP regulatory environment.

Quality Compliance Specialist

  • See description
  • Updated 12/06/2018
  • Limerick

Maintains site compliance of operations in accordance with mandated regulatory requirements and site expectations.

Manager Process Data Monitoring

  • See description
  • Updated 12/06/2018
  • Limerick

Supports the Process Monitoring team through leading the area of process performance monitoring. To establish, organize and maintain the in-process-controls process performance monitoring program and supporting manufacturing activities.

Process Science Associate - Purification

  • See description
  • Updated 12/06/2018
  • Limerick

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

Sr IT Lab Systems Analyst

  • See description
  • Updated 12/06/2018
  • Limerick

The Senior Laboratory Systems Analyst will be responsible for implementation and subsequent day to day support and maintenance of general Laboratory Computers systems in our QC, Chemistry, Micro and Process Sciences labs.

Process Scientist - Manufacturing Support

  • See description
  • Updated 12/06/2018
  • Limerick

Supports the Process Sciences Department with analysis, troubleshooting, and process validation of manufacturing bioprocesses.

QA Validation Specialist

  • See description
  • Updated 12/06/2018
  • Limerick

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

Process Scientist - Process Validation

  • See description
  • Updated 12/06/2018
  • Limerick

Supports the Process Sciences Department with analysis, troubleshooting, and Process Validation of manufacturing bioprocesses.

IT Compliance Analyst/Tech Writer

  • See description
  • Updated 12/06/2018
  • Limerick

The IT Compliance Analyst is responsible for ensuring that the 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 groups.

Regeneron Ireland reviews
(6)

Good Pay and not a great place to work

Anonymous in Limerick, Ireland
former employee in 2016
14/12/2017

The Best Bits

the pay was good and Benefits to mask underlying issues

Things to improve

More experienced mangers , The first in promoted to senior managers and a lot do not have technical or people management abilities

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Please describe the problem with this review.

Happy employee

Anonymous in Dublin, Ireland
current employee in N 2017
31/05/2017

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

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Please describe the problem with this review.

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

Anonymous in Limerick, Ireland
former employee in 2016
30/05/2017

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.

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