Quality Operations API Intern: Docs & Compliance

Bristol-Myers Squibb Co

Dublin

On-site

EUR 23,000 - 29,000

Full time

3 days ago
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Job summary

Bristol Myers Squibb Co offers an internship program in Dublin focused on Quality Operations. The role involves working with the Global API team to support documentation management, change controls, and interdepartmental communications.

The program provides hands-on experience across document workflows and quality systems during a 6 to 12 month period. The position emphasizes collaboration, adherence to GMP, and exposure to regulatory affairs, with a structured learning path and local market

Qualifications

  • Minimum 2 years of science-related academic experience.
  • Knowledge of GMP regulations.
  • Ability to build relationships with external manufacturers.
  • Negotiation, communication and presentation skills.
  • Analytical and problem-solving skills.

Responsibilities

  • Initiate, revise and evaluate change controls with CMOs.
  • Support uploading and approval of protocols, reports and memos in the Document Management System.
  • Prepare Quality Agreements and purchase specs.
  • Support Annual Product Reviews for CMOs.
  • Assist quality council meetings.
  • Follow corporate policies and directives.
  • Support audit observation closure.
  • Review and update CMO Bona Fides.
  • Update annual risk assessments for CMOs.
  • Update stability protocols as necessary.
  • Support quality related projects.
  • Manage the annual Batch Record Review‑Requalification of CMOs.
  • Meet all targets related to BMS metrics.

Skills

Science background
GMP knowledge
Stakeholder relationships
Negotiation skills
Analytical & problem-solving

Education

Science degree or equivalent

Job description

Bristol Myers Squibb Co offers an internship program in Dublin focused on Quality Operations. The role involves working with the Global API team to support documentation management, change controls, and interdepartmental communications.

The program provides hands-on experience across document workflows and quality systems during a 6 to 12 month period. The position emphasizes collaboration, adherence to GMP, and exposure to regulatory affairs, with a structured learning path and local market

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