Pay Rate: €25.00 hourly plus holiday pay
Location On site - Ireland
Atrium (EMEA) are supporting a global biopharma company looking for a QC specialist. Responsible for ensuring medicine safety, efficacy, and regulatory standards by sampling and testing raw materials, in-process products, and finished goods. Operating within Good Manufacturing Practices (GMP) and Good Laboratory Practice (GLP) guidelines.
Key Responsibilities
Liaise with manufacturing to ensure all Drug Product samples are processed and delivered to the appropriate destination in an appropriate timeframe.
Liaise with Warehouse Cryogenics Logistics (WCL) to ensure all Raw Material samples are processed and delivered to the appropriate destination in an appropriate timeframe.
Support the QC readiness and implementation of Drug Product Stability
Release samples for QC testing.
Perform monthly reconciliation and report deviations to Sample Management Manager
Reconstitute samples for the QC activities
Generate and update SOPs and other relevant documents as required.
Maintain a high standard of GMP compliance including the completion and provision of training as required.
Technical Skills Required
The ideal candidate should hold a minimum of a Level 8 degree in Microbiology or related discipline.
At least 1 years’ experience in a pharmaceutical / healthcare laboratory or related technical function.
A strong background in Microbiology or raw materials is desirable but not essential.
The successful candidate must demonstrate excellent written and verbal communication skills.
The ability to work in a team based collaborative environment is essential.
Sterility experience is desirable but not essential.
#J-18808-Ljbffr