Cancel
×
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.

No Recruiter Emails

Overall rating
4.3
Based on 6 employee reviews
5
83%
4
0%
3
0%
2
0%
1
17%
  • Office & Transport links
  • Culture & people
  • Training & development
  • Work/Life balance
  • Career progression
 

Read reviews

 

Email me jobs from Regeneron Ireland

Please enter your email address

Please enter a valid email address

Regeneron Ireland Jobs
(44)

QA Validation Specialist - Cleaning Validation

  • See description
  • Updated 24/02/2018
  • Limerick

QA-Validation Specialist responsible for the development and execution of cleaning validation of process equipment used in the direct manufacture of biopharmaceutical drug substances.

QA Validation Specialist

  • See description
  • Updated 24/02/2018
  • Limerick

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

Assoc Mgr Process Sciences - Manufacturing Support

  • See description
  • Updated 24/02/2018
  • Limerick

Responsible to support the Process Sciences Department through Process Validation, manufacturing floor support, product impact assessments, investigations, and technical evaluation as required.

Process Sciences Project Manager

  • See description
  • Updated 24/02/2018
  • Limerick

Acts as a Project Manager within the Process Sciences department to support operational management and optimization.

Process Scientist - Process Validation

  • See description
  • Updated 24/02/2018
  • Limerick

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

Senior Technical Training Specialist

  • See description
  • Updated 23/02/2018
  • Limerick

Summary: Collaborates with team to ensure business objectives are met through effective learning solutions; administers, oversees and organizes job specific training programs for IOPS (Industrial Operations & Product Supply).

Temp - QC Analyst Raw Materials

  • See description
  • Updated 23/02/2018
  • Limerick

Summary: Performs a variety of chemical or biological analyses on raw materials, products, in-process materials, or stability samples in support of the company's quality program.

Associate Manager Warehouse & Logistics

  • See description
  • Updated 23/02/2018
  • Limerick

Summary: Responsible for the direction, organisation and management of Warehouse & Logistics operations within the pharmaceutical industry.

Associate Manager Technical Training

  • See description
  • Updated 23/02/2018
  • Limerick

Summary: Responsible for leading the technical and regulatory GxP training for the Raheen (IOPS) site.

Sr Statistician

  • See description
  • Updated 23/02/2018
  • Limerick

To establish, organise and maintain effective statistics and data evaluation services pertaining to process monitoring and modelling of biological drugs. To train relevant employees how to effectively employ statistics within their job functions.

Lead QC Micro Analyst II-IV (Sample Management)

  • See description
  • Updated 23/02/2018
  • 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 Analyst Lead Chemistry

  • See description
  • Updated 23/02/2018
  • Limerick

Summary: Performs a variety of chemical analyses on raw materials, final products, in-process materials, or stability samples in support of the company's quality program.

Supervisor QC Micro (Sample Management)

  • See description
  • Updated 23/02/2018
  • Limerick

Summary: Oversee daily operation and communication for samples submitted from Manufacturing, QA Validation, and QC labs. Ensure chain of custody is maintained and timely delivery of samples to the labs.

Senior Compliance Specialist

  • See description
  • Updated 23/02/2018
  • Limerick

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

Qualified Person

  • See description
  • Updated 23/02/2018
  • 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 Systems Specialist - Change Control

  • See description
  • Updated 22/02/2018
  • Limerick

Co-ordinates and maintains the site Change Control process to ensure that this key element of the Quality Management System continuously operates in a compliant manner while meeting ongoing business requirements.

Continuous Improvement Specialist

  • See description
  • Updated 22/02/2018
  • 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.

Quality Systems IT Analyst

  • See description
  • Updated 22/02/2018
  • Limerick

Configures the Qumas DocCompliance and qProcess Compliance software to meet end-user needs.

Principal Automation Infrastructure Engineer

  • See description
  • Updated 22/02/2018
  • Limerick

Summary: Performs advanced technical planning, system integration, maintenance, verification, and validation of PLC and HMI based automated process control systems and process monitoring systems in a biopharmaceutical manufacturing cGMP environment.

Principal Project Engineer

  • See description
  • Updated 22/02/2018
  • Limerick

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

Process Science Associate - Mfg Support

  • See description
  • Updated 22/02/2018
  • Limerick

Supports the Process Sciences Department with on the floor activities, process troubleshooting and process validation of manufacturing bioprocesses.

Principal Process Engineer - Technology Transfer

  • See description
  • Updated 21/02/2018
  • Limerick

The Process Engineer will work with the Manufacturing Sciences and Technology (MSAT) group in Rensselaer, New York to ensure site to site consistency after processes are transferred in Raheen.

Sr Manager Facilities Maintenance

  • See description
  • Updated 21/02/2018
  • 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.

QC Lab Instrumentation Analyst

  • See description
  • Updated 21/02/2018
  • Limerick

Summary: Support the QC and QA departments by maintaining their laboratory instrumentation in an operational, qualified state.

Manager, External Manufacturing Operations Support

The Drug Product Operations Support Manager works with the Drug Product Manufacturing team and will oversee and co-ordinate operations support activities that manufacture Regeneron Products at the External Manufacturing sites.

Associate Lab Systems Analyst

  • See description
  • Updated 21/02/2018
  • 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 in our QC, Chemistry, Micro and Process Sciences labs.

Sr Quality Specialist

  • See description
  • Updated 21/02/2018
  • 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.

Manufacturing Support Specialist

  • See description
  • Updated 21/02/2018
  • Limerick

Summary: Performs tasks related to the support of manufacturing operations (Large Scale & Sub-Suites); primarily the tracking, collation, analysis and presentation of manufacturing operations data & metrics.

Associate Manager External Manufacturing

The Drug Product Associate Manager works with the DP team to oversee and co-ordinate the supply of Regeneron Products at the External Manufacturing sites.

Manager QC Microbiology (Micro Support)

  • See description
  • Updated 20/02/2018
  • Limerick

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

Sr Mgr Process Sciences - Downstream

  • See description
  • Updated 20/02/2018
  • 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.

IT MES Analyst

  • See description
  • Updated 20/02/2018
  • Limerick

Responsible for the overall system maintenance and on-going support of the Manufacturing Execution Systems (MES).

Quality Compliance Specialist

  • See description
  • Updated 20/02/2018
  • Limerick

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

Sr Process Scientist - Purification

  • See description
  • Updated 20/02/2018
  • Limerick

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

Quality Specialist

  • See description
  • Updated 20/02/2018
  • Limerick

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.

Process Scientist - Process Monitoring

  • See description
  • Updated 20/02/2018
  • Limerick

To provide statistical support and promote the use of statistical thinking across the site. To establish, organise and maintain effective statistics and data evaluation services pertaining to process monitoring and modelling of biological drugs.

QA Validation Specialist - Review

  • See description
  • Updated 20/02/2018
  • Limerick

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

Mgr/Sr Mgr CMC Program Management

  • See description
  • Updated 20/02/2018
  • 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.

Senior Materials Planner

  • See description
  • Updated 19/02/2018
  • Limerick

Summary: Functions as part of Materials Management/Supply Chain by determining resources needed to meet manufacturing production schedule.

Sr Compliance Specialist - Process Sciences

  • See description
  • Updated 19/02/2018
  • Limerick

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

Director, Program Operations Lead

The Program Operations Lead (POL) is responsible for leadership and overall strategic management of one or more complex programs in Clinical Trial Management (CTM).

Senior Manager QC Bioanalytics

  • See description
  • Updated 16/02/2018
  • 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.

Senior Manager QC Chemistry

  • See description
  • Updated 16/02/2018
  • 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.

Sr Manager QC Support

  • See description
  • Updated 16/02/2018
  • 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.

Regeneron reviews
(6)

Good Pay and not a great place to work

Anonymous in Limerick, Ireland
former employee in 2016
28/11/2017

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

Report

Please describe the problem with this review.

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.

Report

Please describe the problem with this review.

Twitter

We use cookies to customise our website for you, giving you the best possible user experience. If you continue without changing your settings, we’ll assume that you are happy to receive this personalisation. Find out more about our cookie policy

Accept & Close