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
R&D Engineer
Dublin
Administration Support
Dublin North
QA Manager Biologics
Dublin West
QA Manager
Dublin North
Snr QA Specialist
Dublin South
Biostatistician
Dublin City Centre
Senior Buyer
Dublin
Program Manager
Westmeath
QC Manager
Galway
Automation Technician
Dublin South
Supply Chain Analyst
Dublin North
QA Manager
Meath
QA Manager
Dublin West
R&D Engineer
Galway
API Purchaser
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

Laboratory Coordinator


Reference:AHWD-147267 Location: Dublin
Qualification:DegreeExperience:4-5 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Laboratory Scientist, QC Analyst

Laboratory Coordinator
Our client, a global pharmaceutical organisation are currently recruiting for a Laboratory Coordinator to join their organisation. This role will sit with the Quality Systems Group and report directly into the Quality Systems Manager.

Responsibilities
• Assist in delivering on key objectives in relation to Method Transfers between in-network and 3rd party laboratories in line with GMP, GLP and safety requirements.
• Provide technical support and troubleshooting as required for in-network and 3rd party laboratories
• Coordinate and manage stability placement with 3rd party labs
• Manage the review of stability data within the Regional team
• Schedule, coordinate and report on Product Launch Method transfers
• Coordinate projects related to Laboratory requirements on behalf of EMEA region, as required.
• Manage laboratory investigations and completion of reports within the required timelines
• Review and approval of AMT reports for EMEA region
• Highlight any discrepancies, deviations or non-conformance’s in testing or work practice which may impact on achieving project deadlines or customer delivery
• Review testing schedules with the release teams to meet dispatch requirements.
• Provide technical support to in-network and 3rd party Laboratories
• Have an overview of all relevant projects ongoing within the Quality department relating to Contract and 3rd Party testing of products
• Adhere to and maintain the quality systems relating to 3rd party testing
• Approve and investigate analytical issues/deviation reports and change controls as required
• Escalate stability OOS results through the escalation system
• Maintain a state of audit readiness for in-network/3rd party systems
• Ensure that the systems with a GMP impact are maintained as per written procedures

Requirements
• Minimum of a Bachelor Degree in Science or related pharmaceutical discipline
• At least 5 years pharmaceutical Quality experience is desirable, ideally within a QC environment
• Excellent interpersonal skills
• Experience in a high volume environment
• Track record with the HPRA/FDA is desirable
• A proven identifiable track record of success in a similar environment
• Experience in managing change and seeking continuous improvements
• Good Computer skills are required


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

Sinead Cullen | Tel: +353 (0) 1 507 9252