Job Title:
QC Material Management Analyst – Contract
Duration:
12 months
Location:
Cruiserath, Dublin – Hybrid
Hourly Rate:
€19.72 per hour – PAYE engagement
This role does not offer sponsorship.
Job Description:
The QC Material Management Analyst will join the QC Site Operations team at a leading biopharmaceutical facility in Cruiserath, Dublin. Reporting to the QC Material Management Supervisor, this role is responsible for performing raw material testing, in-process sample analysis, and laboratory duties in compliance with cGMP regulations.
Responsibilities:
* Perform QC testing of water samples (TOC, pH, Conductivity).
* Conduct raw material analysis using techniques including HPLC, KF, UV, IR, and wet chemistry.
* Complete laboratory documentation accurately and on time.
* Ensure compliance with Standard Operating Procedures (SOPs) and registered specifications.
* Author and review laboratory documentation, including SOPs.
* Perform batch paperwork reviews and reconcile laboratory analyses.
* Investigate and document out-of-specification results in line with site procedures.
* Support technical transfer of new projects.
* Assist with deviation and out-of-specification investigations using the Infinity system.
* Manage samples, maintaining chain of custody using CIMS and LIMS.
* Stay up to date with corporate and industry compliance requirements for laboratory operations and aseptic manufacturing.
* Carry out any additional duties as directed by the Lab Supervisor.
Requirements:
* Third level qualification (Degree) in Chemistry, Biology, or a related discipline.
* 2–3 years' experience in a pharmaceutical/healthcare laboratory or related technical function.
* Strong written and verbal communication skills.
* Ability to work effectively in a collaborative, team-based environment.