Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

We are recruiting QC Laboratory Assistant to join our diverse team in Cork.

In this role you will provide key support to all laboratory activities in relation to:

cGMP Documentation ControlInventory ManagementSample ManagementAdministration and Technical SupportTraining Administration Support

Role & Responsibilities:

GMP Documentation Control

Issuance of Laboratory cGMP Documentation; Laboratory Notebooks, Datasheets, Labels and LogbooksQC Department SME on the Document Management System OneVaultUpdate Standard Operating Procedures and Datasheets on Word and OneVaultManagement of QC Department archiving

Inventory Management

Order Laboratory consumable (PO creation and reconciliation of invoices) on SAP/SRMSupport Site SRM purchasing as requiredReceipt and collection of QC Laboratory ConsumablesSupport implementation and maintenance of Kanban system for Laboratory ConsumablesCreate and maintain relationships with external vendors in relation to ordering, lead times etc.

Sample Management

Shipment of samples from Abbvie Cork QC Laboratory to Third Party LaboratoriesCommunication of documentation updates to Third Party Laboratories

Administration and Technical Support

General Administration Support for the QC LaboratoryAdhere to cGMP and GLP requirementsGeneral Technical Support (as required), log in/verification of reagents to Sample Manager

Training Administration Support

Support QC training administration on LMS Compliance Wire

Qualifications
Leaving Certificate or equivalent  Quality Control qualification an advantage.Understanding of cGMP requiredPrevious experience in a pharmaceutical manufacturing environment is desirable but not essential
Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html 

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html