QC Sample Management Specialist

Bristol Myers Squibb; Fingal; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Annual bonus

Pension contribution

Family health insurance

27 days annual leave

On-site gym

Life assurance

Job summary

Bristol Myers Squibb is seeking a Specialist, QC Sample Management to support sample processing across Drug Substance, Drug Product, and stability workflows at Cruiserath. You will manage sample logging, storage, release for QC testing, and ensure GMP-compliant operations in a fast-paced biotech environment.

The role offers growth, comprehensive benefits, and a collaborative culture that prioritizes patient outcomes, inclusion, and continuous improvement.

Responsibilities

• Liaise with manufacturing to ensure all Drug Substance samples are processed and delivered to the appropriate destination in an appropriate timeframe.
• 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 implementation and execution of Drug Product Stability at Cruiserath
• Manage TempTales and shipping documents when receiving samples from external sites.
• Logging of samples to LIMS/CIMS or logbooks, and label accordingly.
• Release samples for QC testing.
• Storage of backups and reserve samples.
• Perform monthly reconciliation and report deviations to Sample Management Manager, if any.
• Reconstitute and Aliquot samples for the QC activities for Global Biologics Laboratory, Global Stability and Multi Product Cell Culture (MPCC) Facility.
• Support buffer preparation for the QC Separations lab
• Support enrolment of bulk Drug Product Stability Study Samples
• Support timepoint pulls of Drug Product Stability Study Samples
• 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.
• Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
• Support continuous improvement initiatives across the department and within the team
• Performing any other activities as indicated by the Lab Manager.

Job description

Bristol Myers Squibb is seeking a Specialist, QC Sample Management to support sample processing across Drug Substance, Drug Product, and stability workflows at Cruiserath. You will manage sample logging, storage, release for QC testing, and ensure GMP-compliant operations in a fast-paced biotech environment.

The role offers growth, comprehensive benefits, and a collaborative culture that prioritizes patient outcomes, inclusion, and continuous improvement.