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

QC Laboratory Technician Shift (Incoming QC)


Reference:RK21180 Location: Carlow
Qualification:DegreeExperience:1-2 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: QC Analyst

QC Laboratory Technician Shift (Incoming QC)
RK21180
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.



Duties:

  • Movement of materials across the network.
  • System transactions including movement and shipping of samples across QC labs within the network.
  • Knowledge and experience using systems such as GLIMS, LIMS and SAP beneficial.
  • Inspection of primary packaging
  • Participate in writing/revising/ rolling out accurate operational procedures, training materials and maintenance procedures for various Quality systems; ensure all work is carried out in line with same.
  • Where applicable, review, approve and trend test results.
  • Peer review other analysts documentation, ensuring QC Right First Time KPIs are achieved.
  • Participate in QC daily meetings and ensure effective communication of testing progress, deviations etc.
  • Ensure that all Quality Systems within the department are adhered to on a daily basis.
  • Complete all documentation in compliance with GMP and GxP standards.
  • Problem solving to get to root cause of issues.
  • Provide support with audit/inspection requirements to ensure department compliance/readiness.
  • Collaborating with others by sharing your skill-set and expertise
  • Drive continuous improvement, perform root cause analysis on system failures e.g. FMEA, Fishbone diagrams, 5 why's etc,
  • Drive compliance with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions, including maintenance of accurate records.



Education and Experience :
  • Degree in Science, Engineering or similar
  • 1 - 3 years’ experience in the Pharmaceutical, Biopharmaceuticals industry or a similar operating environment which includes experience in a Quality function.
  • Previous Analytical Experience
  • Knowledge of US and European cGMP guidelines, and other international regulatory requirements, as applicable to the site.

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