Role:
QC Material Management Analyst
Role Location:
North Dublin
Role Type:
12 month contract
We are seeking to recruit a QC Material Management Analyst to join the QC Site Operations team at a Multi-Product Cell Culture Drug Substance Facility in North Dublin
Reporting to the QC Material Management Supervisor, you will be responsible for supporting site activities related to performing testing of Raw Materials, in-process samples and laboratory duties in accordance with cGMP regulations.
The main responsibilities for this position include;
· Performing QC testing (TOC, pH Conductivity) of water samples. Performing analysis of Raw Materials including HPLC, KF, UV, IR and wet chemistry techniques. Completion in a timely and accurate manner of laboratory documentation as directed by the QC Material Management Supervisor.
· Compliance with Standard Operating Procedures and Registered Specifications.
· Assisting in authoring and reviewing documentation, including SOPs, as required.
· Batch paperwork review, and reconciliation of analysis performed in laboratory. Ensuring that any out of specification results are investigated according to site procedures.
· Supporting technical transfer of new projects.
· Assisting with out of specification investigations and deviations using the Infinity system.
· Sample management activities- ensuring chain of custody is maintained using CIMS and LIMS.
· Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
· Performing any other activities as indicated by the Lab Supervisor.
The successful candidate must demonstrate excellent written and verbal communication skills and the ability to work in a team based collaborative environment.
The ideal candidate should hold a minimum of a third level qualification (Degree) in Chemistry/Biology or related discipline along with at least 2-3 year of experience in a pharmaceutical / healthcare laboratory or related technical function.