GMP‑Driven QC Sample Management Intern

Bristol Myers Squibb

Fingal

On-site

EUR 22,000 - 27,000

Full time

14 days+

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Job summary

Bristol Myers Squibb is offering a QC Sample Management Intern position within the QC Materials team at Cruiserath, Dublin. This internship provides hands-on experience in sample management, cGMP compliance and laboratory operations, with mentorship and structured training.

You will support sample processing, logging, and documentation, while developing practical skills in a pharmaceutical lab and contributing to continuous improvement initiatives.

Qualifications

  • Minimum third-level qualification in Chemistry or Biology.
  • At least 1 year of experience in a pharmaceutical/healthcare laboratory.
  • Excellent written and verbal communication in a team environment.

Responsibilities

  • Coordinate with manufacturing to route Drug Substance samples in time.
  • Coordinate with Engineering Stores for Drug Product samples delivery.
  • Manage TempTales and shipping documents for external samples.
  • Log samples in LIMS/CIMS or logbooks and label accordingly.
  • Store backups and reserve samples.
  • Perform monthly reconciliation and report deviations to Lab Manager.
  • Support buffer preparation for the QC Separations lab.
  • Generate and update SOPs and other relevant documents.
  • Maintain GMP compliance and complete required training.
  • Keep abreast of industry requirements affecting lab operations.
  • Support continuous improvement initiatives.
  • Perform other Lab Manager indicated tasks.

Skills

Communication skills
Team player

Education

Degree in Chemistry/Biology

Tools

LIMS/CIMS

Job description

Bristol Myers Squibb is offering a QC Sample Management Intern position within the QC Materials team at Cruiserath, Dublin. This internship provides hands-on experience in sample management, cGMP compliance and laboratory operations, with mentorship and structured training.

You will support sample processing, logging, and documentation, while developing practical skills in a pharmaceutical lab and contributing to continuous improvement initiatives.

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