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
Claire Kenny
Life Science

+353 1 507 9287
claire.kenny@lifescience.ie
Connect with me on
Administration Support
Dublin North
Planner/Buyer
Limerick
R&D Engineer
Dublin
Demand Planner
Limerick
Process Engineer
Limerick
QC Trainer
Cork
Project Manager
Kilkenny
CTO
Galway
QC Chemist
Dublin
QA Specialist
Dublin
Consultant
Cork
Program Manager
Westmeath
API Purchaser
Dublin
Quality Manager
Dublin South
R&D Engineer
Dublin
Quality Engineer
Limerick
Risk Manager
Dublin
Quality Engineer
Dublin South
Senior Social Work Practitioner
Republic of Ireland
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

Quality Control Analyst (Biopharma)


Reference:CK/A000000(ALXW-573854) Location: Carlow
Qualification:DegreeExperience:1-2 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Quality Control Supervisor, QC Analyst

Quality Control Analyst – Biopharma, Carlow

Our client, a top tier biopharmaceutical company is looking for a number of Quality Control Specialists to join their team in Carlow.
The Quality Control Specialist co-ordinates quality control activities as required relating to product schedules including any project work to ensure processes and end products comply with corporate and regulatory requirements to facilitate product release.
Responsibilities:
Drive compliance with Company policies, procedures and guidelines and regulatory requirements and execute Good Manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
Facilitate / Attend meetings for QC function to confirm all testing and validation activities are on schedule.
Provide oversight for the selection and management of external testing Laboratories.
Ensure all external laboratory quality agreements are in place and adequately cover all applicable testing.
Coordinate QC equipment projects including purchasing and ensuing validation.
Provide support with audit/inspection requirements to ensure department compliance/readiness. Participate in internal and external audits and inspections, taking the role of auditee for assigned areas of responsibility.
Drive continuous improvement, perform root cause analysis on system failures and substandard equipment performance, using standard tools and methods, to resolve machine and system issues.
QC representative for new product introduction.
Qualifications, Skills & Experience Required:
1 - 3 years’ experience in the Pharmaceutical, Biopharmaceuticals industry or a similar operating environment which includes experience in a Quality function.
Previous Analytical Experience
Experience in Material/Laboratory Qualification
Degree in Science, Engineering or similar
Lean Six Sigma Yellow Belt or suitable alternative
Knowledge of cGMP in Laboratory Quality Systems


Claire Kenny | Tel: +353 (0) 1 507 9287