Metrology Intern – Specialist Documentation & Data Management

Bristol Myers Squibb

50% onsite
Metrology documentation updates
Cmms data control and updates
Cgmp and bms standards
Bristol Myers Squibb is seeking a Metrology Intern focusing on Specialist Documentation & Data Management, requiring a background in technical disciplines related to quality and calibration. The role involves updating and organizing calibration documentation, ensuring compliance with industry standards, and supporting cross-functional teams. Candidates should possess strong analytical skills and a basic understanding of metrology concepts, with French language skills being essential

Job Summary

  • The Metrology Intern supports the Metrology team in updating, organizing, and maintaining calibration related documentation and ensuring alignment with current metrology processes.
  • The role contributes to improving data integrity, documentation compliance, and harmonization of metrology records in accordance with current Good Manufacturing Practice (cGMP) and internal Bristol Myers Squibb (BMS) standards.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Metrology Intern focusing on Specialist Documentation & Data Management, requiring a background in technical disciplines related to quality and calibration. The role involves updating and organizing calibration documentation, ensuring compliance with industry standards, and supporting cross-functional teams. Candidates should possess strong analytical skills and a basic understanding of metrology concepts, with French language skills being essential.

Skills & Requirements

Must-have

  • Metrology documentation updates
  • CMMS data control and updates
  • cGMP and BMS standards
  • Good documentation practices
  • Technical document interpretation

Nice-to-have

  • Interest in pharmaceutical operations
  • Interest in Documentation management systems
  • Interest in CMMS/asset management systems
  • Work rigor and organization
  • Cross-functional coordination support

Key Requirements

  • Technical discipline (CFC of polymechanic or equivalent)
  • Experience in quality / document management / metrology
  • French required
  • MS Office (Word, Excel) proficiency

Work Rights

Not specified

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