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
CSV Engineer
Dublin
Risk Manager
Dublin
Administration Support
Dublin North
API Purchaser
Dublin
Senior Social Work Practitioner
Republic of Ireland
Project Manager
Kilkenny
Quality Engineer
Limerick
R&D Engineer
Dublin
Quality Manager
Dublin South
R&D Engineer
Dublin
Program Manager
Westmeath
Process Engineer
Limerick
QC Trainer
Cork
Quality Engineer
Dublin South
QA Specialist
Dublin
Planner/Buyer
Limerick
CTO
Galway
Biostatistician
Dublin City Centre
QC Chemist
Dublin
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

QC Analyst (Chromatography)


Reference:SMC035742 Location: Cork
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: IT Analyst, QC Analyst


We’re currently recruiting for an exciting opportunity with an award winning pharmaceutical organization based in Cork. 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

• Achieves competency in laboratory methods and procedures, specifically compendial Wet Chemistry techniques.
• Performs analytical testing activities in relation to material release.
• Performs routine and non-routine analytical testing activities.
• Review and approval (where appropriate) of laboratory test results.
• Ensures that testing and results approval are completed within agreed turnaround times.
• Writes and reviews laboratory TMs, SOPs and WIs as directed by company policy.
• Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
• Is an active member of the QC group and provide assistance with other group activities as required and communicates relevant issues to the QC Team Leader and Manager.
• Deals with non-conformances/ deviations in an accurate and timely manner.
• Maintains and develops knowledge of analytical technology as well as cGMP standards.

Education & Experience

• A third level qualification in a scientific/technical discipline required.
• Knowledgeable of FDA/EMEA regulatory requirements applicable to pharmaceuticals.
• Demonstrated knowledge and testing experience in an FDA/HPRA approved QC laboratory.
• A minimum of 2 years experience in a laboratory-testing environment within the pharmaceutical industry would be an advantage.

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

Sean McCarthy | Tel: +353 (0) 87 798 8480