I'm looking for...
close

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

crome
Google Chrome
IE
Internet Explorer
firefox
Mozilla Firefox
opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Contact Info
Consultant
Cork
Quality Engineer
Dublin South
Program Manager
Westmeath
API Purchaser
Dublin
R&D Engineer
Dublin
R&D Engineer
Dublin
Risk Manager
Dublin
Administration Support
Dublin North
R&D Engineer
Limerick
Quality Manager
Dublin South
QA Specialist
Dublin
QC Analyst
Cork
CQV Engineer
Dublin
R&D Engineer
Galway
Microbiology Manager
Republic of Ireland
QC Trainer
Cork
CTO
Galway
Senior Social Work Practitioner
Republic of Ireland
GMP Inspector
Dublin
Quality Engineer
Limerick
Process Engineer
Limerick
Apply for this job

Name:

Surname:

Email:

Phone:

Cv:

Salary Expectations:

Education:

Experience:

Current Location:

Notice Period:

Write here your cover note:


If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to applications@lifescience.ie
Details

Manufacturing Specialist (MES)


Reference:PORAQDM-523332 Location: Dublin
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: EHS Specialist, Manufacturing Executive

Manufacturing Specialist (MES)


The Role

A Manufacturing Specialist (MES) is required to join a global pharmaceutical organisation in Dublin. Reporting into the Manager Manufacturing (MES) you will be responsible for development, configuration and testing of Master Batch Records (MBRs) from initial to final design. The successful candidate will have at least five to ten years of experience in a pharmaceutical or biotech industry and will have demonstrated competency in leading teams to deliver complex MBR designs in time with project timelines.


The Person

  • Responsible for the development, configuration and testing of Master Batch Records (MBRs) from initial to final design.
  • Responsible for leading MBR development design reviews including liaising with Operations, Process Development and Quality functions.
  • Responsible for drafting, executing and reviewing Application Lifecycle Management test scripts and test sets for testing MBR design.
  • Responsible for the support and ongoing development of the MES system in development of MBRs and improving the MES business process.
  • Responsible for training of Electronic Batch Record (EBR) end-users (Supervisors, Operators, Technical/QA/Support staff).
  • Responsible for the development, review and update of MES Standard Operating Procedures.
  • Responsible for the preparation and management of MBR change requests and associated change request forms (and other documentation) in a timely manner by liaising with customers, System Owner etc.
  • Accountable for adherence to established timelines and metrics for the change control and CAPA process.


The Person

  • Bachelor’s degree in Engineering or Science
  • Knowledge of regulation requirements (GMP & EH&S)
  • Typically 5 – 10 years’ experience in a pharmaceutical environment
  • Broad technical experience in MES systems



If you would like further Information you can contact the recruiter directly:



Paula O'Reilly | Tel: +353 (0) 1 507 9265