QC Material Management Analyst

PE Global (UK); Cruiserath; On-site; EUR 35,000 - 50,000; Full time

Job summary

PE Global (UK) is looking for a contract position in Cruiserath, Dublin. The role involves liaising with manufacturing and engineering stores to ensure timely processing and delivery of drug samples. Ideal candidates will have a degree in Chemistry or Biology and at least one year of relevant laboratory experience.

Responsibilities include performing QC testing of samples, managing documents, maintaining compliance with procedures, and assisting in documentation. Candidates are expected to have strong analytical skills and experience with laboratory techniques such as HPLC.

Qualifications

• Minimum of a third-level qualification in Chemistry, Biology or related discipline.
• 1 year of experience in a pharmaceutical or healthcare laboratory.

Responsibilities

• Liaise with manufacturing to ensure timely process of Drug Substance samples.
• Manage TempTales and shipping documents for samples received.
• Perform QC testing of water samples and analyze Raw Materials.

Skills

Laboratory analytical techniques

Quality Control testing

Standard Operating Procedures

Education

Degree in Chemistry, Biology or related discipline

Tools

HPLC

LIMS/CIMS

Job description

Role

Contract position.

Responsibilities

• Liaise with manufacturing to ensure all Drug Substance samples are processed and delivered to the appropriate destination in an appropriate timeframe.
• Liaise with Engineering Stores 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.
• Manage TempTales and shipping documents when receiving samples from external sites.
• Log samples into LIMS/CIMS or logbooks, and label accordingly.
• Release samples for QC testing.
• Store backups and reserve samples.
• Perform monthly reconciliation and report deviations to Sample Management Lead, if any.
• Aliquot samples for the QC activities for Global Biologics Laboratory and Multi Product Cell Culture (MPCC) Facility.
• Perform QC testing (TOC, Nitrates, Conductivity) of water samples; analyze Raw Materials using HPLC, KF, UV, IR and wet chemistry techniques; complete laboratory documentation in a timely and accurate manner as directed by the QC Material Management Supervisor.
• Comply with Standard Operating Procedures and Registered Specifications.
• Assist in authoring and reviewing documentation, including SOPs, as required.
• Review batch paperwork, reconcile laboratory analyses, and investigate any out‑of‑specification results according to site procedures.

Qualifications

• Hold a minimum of a third‑level qualification (Degree) in Chemistry, Biology or a related discipline.
• Have 1 year of experience in a pharmaceutical or healthcare laboratory or a related technical function.