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
QA Manager
Meath
API Purchaser
Dublin
Head of Quality
Dublin West
Buyer
Cork
Snr QA Specialist
Dublin South
QA Officer
Dublin
Biostatistician
Dublin City Centre
R&D Engineer
Dublin
Program Manager
Westmeath
QA Manager
Dublin North
R&D Engineer
Galway
QA Manager
Dublin West
QA Manager Biologics
Dublin West
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 Officer


Reference:AVVM-100365 Location: Dublin
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: QA Analyst, QA Specialist

JOB PURPOSE
The Quality Assurance Officer is responsible for supporting Quality Systems and ensuring GMP compliance across the site.

KEY TASKS AND RESPONSIBILITIES
• Review all manufacturing and packaging batch documentation including electronic and paper batch records, for both pharmaceutical and medical device products.
• Preparation of Annual Product Quality Review reports.
• Effective management and control of the process deviation system, including timely preparation of deviation investigation reports.
• Effective management and control of the change control system, ensuring all change controls are approved in a timely manner.
• Co-ordination of investigations, reports and responses to customer complaints within the required timelines.
• Review and approval of vendor files.
• Liaising with suppliers to resolve supplier complaints.
• Participation in internal audits.
• Assisting in preparation for and participation in regulatory and customer audits.
• CAPA management.
• Participation in Risk Assessments / Root Cause Analysis etc.
• Generation and reporting of Quality metrics monthly.
• Participation in training initiatives including preparation and delivery of GMP training modules and any other training modules as required, for plant personnel.
• GMP documentation preparation, review, approval and management.
• Material Status Control activities.
• Participation in GMP and Continuous Improvement projects within QA and on site.
• Other duties as required and as directed by the Quality Assurance Manager.

SKILLS, EXPERIENCE AND QUALIFICATIONS
• A Bachelor's degree in a Science related discipline.
• Knowledge of EU quality-related pharmaceutical regulations.
• A minimum of 5 years’ experience of working in a similar Quality Assurance related role in the Pharmaceutical Industry.
• Excellent written and verbal communication skills.
• A high standard of report writing.
• Strong attention to detail.
• Excellent organisation skills.
• Good IT skills.
• Good decision making skills.
• The ability to be self-driven and capable of working on own initiative.
• Proven capability of team participation.
• Will be proactive and flexible.






Clodagh Nerney | Tel: +353 (0) 1 507 9254