Forgot your Password?
Find this page useful? Click

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.

Google Chrome
Internet Explorer
Mozilla Firefox

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job






Salary Expectations:



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

IPC Analyst

Reference:SMC35906 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 biopharmaceutical 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.

• Achieves competency in laboratory methods and procedures.
• Trains other QC analysts in laboratory methods and procedureswhen required.
• Performs analytical testing activities in relation to methodvalidation and technical transfer activities to ensure that allmethods meet ICH, USP and EP guidelines.
• Executes validation, operation, maintenance, calibration andtroubleshooting of equipment and its associated software.
• Writes, executes, reports and reviews IQ/OQ and PQ protocols toensure that all relevant equipment is qualified for cGMP use.
• Performs routine and non-routine analytical testing activities.
• Review and approval (where appropriate) of laboratory testresults.
• Ensures that testing and results approval are completed withinagreed turnaround times.
• Writes and reviews laboratory TMs, SOPs and WIs as directed bycompany policy.
• Ensures QC activities are carried out in compliance with productlicense commitments, cGMP and company quality standards.
• Is an active member of the QC group and provide assistance withother group activities as required and communicates relevantissues to the QC Team Leader and Manager.
• Deals with non-conformances/deviations in an accurate andtimely manner.
• Deputizes for the QC Team Leader as appropriate.
• Maintains and develops knowledge of analytical technology aswell as cGMP standards.
• In process control testing and activities to support the productionunits.

Education & Experience
• A third level qualification of a scientific/technical discipline isrequired.
• Knowledgeable of FDA/EMEA regulatory requirements applicableto biologics and/or pharmaceuticals.
•Key analytical technique required: HPLC
•Other desirable techniques: A280 and Nephelometry testing, residual protein assay, TOC analysis

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

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