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
Quality Engineer
Limerick
CQV Engineer
Dublin
R&D Engineer
Galway
Process Engineer
Limerick
QA Specialist
Dublin
R&D Engineer
Dublin
R&D Engineer
Dublin
Quality Engineer
Dublin South
Microbiology Manager
Republic of Ireland
Administration Support
Dublin North
Risk Manager
Dublin
CSV Engineer
Dublin
Quality Manager
Dublin South
Consultant
Cork
CTO
Galway
Senior Social Work Practitioner
Republic of Ireland
API Purchaser
Dublin
R&D Engineer
Limerick
Production Manager
Dublin City Centre
Program Manager
Westmeath
QC Trainer
Cork
QC Analyst
Cork
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

QA Specialist


Reference:SMC034000 Location: Cork
Qualification:DegreeExperience:1-2 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: QA Validation Specialist, QA Specialist

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

QA Specialist

Job Purpose
Managing compliance activities and QA operational activities related to operational project as required by Good Manufacturing Practice (GMP). These activities include, C&Q and Validation activities, Data Integrity and CSV support, change control, non-conformance investigations, compliance auditing, and other related quality system elements.

Duties:

• Supports GMP activities from operational through to Laboratory support programs.
• Partners with other Departments to ensure that compliance programs are completed in an efficient manner and are effectively maintained.
• Responsible for implementation of systems and procedures for the management of change control and deviation management, as it applies to plant installations, systems, and operations in accordance with GMP.
• Quality oversight of project activities including but not limited to, C&Q activities and process validation through to commercial manufacture.
• Participates as a key quality member in inspections and audits of JSCI by external parties/agencies.
• Key participant within the QA team in the execution of their duties.
• Executes the activities of the group within quality to create a synergistic approach to goals and tasks.
• Domestic and international travel may be required.

Desirable:

• Bachelors Degree in a scientific/technical discipline required
• Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.
• Focus on patients and customers at all times.
• Advanced degree (MS, MBA, PhD) preferred
• Experience in C&Q, and Process validation
• Experience in direct interactions with regulatory agencies during site inspections.


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

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