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
Rachel Kent
Life Science

+353 87 427 8808
[email protected]
Connect with me on
Medical Device Director
Republic of Ireland
Senior Manufacting Engineer
Republic of Ireland
Project Engineer
Republic of Ireland
CQV Lead
Tipperary
R&D Director
Galway
R&D Engineer
Galway
C&Q Lead
Tipperary
R&D Engineer
Galway
R&D Manager
Galway
Project Engineer
Limerick
R&D Manager
Galway
Project Enginer
Dublin South
Head of R&D
Galway
Product Lead
Dublin
Process Engineer
Limerick
Project Engineer
Tipperary
Responsible Person (RP)
Republic of Ireland
Senior Quality Engineer-Remote
Republic of Ireland
R&D Manager
Connaught
QA Engineer
Leitrim
Quality Specialist
Tipperary
Account Manager UK and Ireland
Republic of Ireland
R&D Engineer
Galway
R&D Manager
Connaught
R&D Manager
Galway
R&D Engineer
Galway
QA Manager
Canada
R&D Engineer
Clare
Senior Recruitment Consultant
Republic of Ireland
Biostatistician
Dublin City Centre
Chemical Engineer
Tipperary
R&D Engineer
Galway
Qualified Person
Limerick
Senior Recruitment Consultant
Republic of Ireland
R&D Manager
Connaught
Project Manager
Limerick
R&D Engineer
Clare
R&D Director
Galway
QA Manager
Canada
R&D Manager
Galway
R&D Engineer
Dublin
Recruitment Consultant
Republic of Ireland
Biostatistician
Dublin City Centre
Qualified Person
Limerick
R&D Engineer
Dublin
R&D Director
Galway
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 [email protected]
Details

Quality Control Specialist (hybrid)


Reference:RK22140 Location: Carlow
Qualification:DegreeExperience:2-3 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Quality Specialist

Quality Control Specialist (hybrid)
RK22140
11 Months
Carlow


We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.



This position will support all aspects of New Material Introduction process and associated supplier changes ensuring effective interaction with other departments/global teams on matters related to new material introduction and associated qualification as well as support selection and management of external testing Laboratories ensuring all outsourced methods are validated and suitable for the product/material required.


Duties:

• Work as directed by the Quality Control Manager according to Company safety policies, cGMP and cGLP
• Facilitate and drive effective communication to ensure success through representation of QC team on tier meetings
• Support all aspects of New Material Introduction process ensuring effective interaction with other departments/global teams/ external contract testing labs on matters related to new material introduction, supplier changes and associated qualification
• Participate and support Internal/External Investigations
• Coordinate the creation/ update to Quality standards for raw materials and components at Carlow. Complete impact assessments for change controls related to Carlow processes
• Coordinate any efficiency/ increased Lab capability projects as detailed by Quality Control Manager
• Provide support with audit/inspection requirements to ensure department compliance/readiness. Participate in internal and external audits and inspections, taking the role of auditee for assigned areas of responsibility
• Coordination, ownership, and author as required for Annual Product Review
• Participate in Quality Risk Management



Education and Experience :

• Bachelor’s Degree or higher preferred; ideally in a science related discipline

• 2-4 years of experience in a cGMP laboratory environments

• Knowledge of or previous experience in New Material Introduction process



If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or [email protected] for further information.