Senior QC Associate
We are currently recruiting for an exciting opportunity with a leading Pharmaceutical organization based in Dublin. This is an excellent position for anyone looking to join a multinational company that excels in its field.
Key Responsibilities:
* Sample and data management, including sample distribution, LIMS logging, and shipment receipt.
* Stability Program activities such as pulling stability samples and study initiations.
* Creating and approving protocols, sample plans, SOPs, and training manuals.
* Performing SAP, LIMS, and CIMS functions and transactions within the sample management remit.
* Responsible for sample management equipment maintenance, out-of-hours responder duties, and training compliance.
* LIMS data coordination for commercial and import batches.
* Managing site inventory of reference standards, assay controls, and training verification samples.
* QC Representative for NPI activities and routine product meetings.
* Liaising with site planning, manufacturing, and inspection teams regarding manufacturing schedules and QC testing.
Requirements:
* Bachelor's degree in a science-related field.
* 5+ years of biopharmaceutical QC experience or related quality control or GMP laboratory experience.
* 2+ years of specific sample management and stability program experience (desirable).
Desirable Skills:
* Quality control
* Sample Management
* GMP