QA Operations Intern: GMP, Documentation & Quality

Bristol Myers Squibb

Fingal

On-site

EUR 22,000 - 27,000

Part time

14 days+

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Job summary

Bristol Myers Squibb in Ireland is offering a QA Operations Intern position in a dynamic, purpose-driven environment. You will gain hands-on experience in QA processes, batch records, and regulatory readiness while contributing to continuous improvements.

The internship spans six, nine, or twelve months and emphasizes collaboration, training, and real-world exposure to quality systems. Join a team that supports patients and career growth.

Qualifications

  • Chemical & pharmaceutical sciences or related discipline.
  • Strong communication skills and teamwork.
  • Willingness to learn and collaborate in teams.

Responsibilities

  • Support the Qualified Person disposition process for Drug Substance/Drug Product.
  • Support QA Manufacturing Operations shift team and batch record review.
  • Conduct QA review and approval of functional area documentation.
  • Support the disposition process for Working Cell Banks to ensure timely release.
  • Interface with departments to ensure compliance with GMP/regulatory requirements.
  • Liaise with Supply Chain and Quality to meet disposition lead times.
  • Prepare and present Quality metrics to support batch records and investigations.
  • Support site inspection readiness and GMP documentation progression.
  • Assist with Annual Product Quality Reviews administration.
  • Authoring, review and approval of QA procedures.
  • Identify and implement continuous improvements within QA group.
  • Engage in Quality Culture initiatives.

Skills

Strong communication skills
Teamwork
Motivated

Education

Chemical & Pharmaceutical Sciences, Pharmacy, Biomolecular & Biomedical Science or Pharmaceutical & Biomedical Chemistry discipline of study

Tools

N/A

Job description

Bristol Myers Squibb in Ireland is offering a QA Operations Intern position in a dynamic, purpose-driven environment. You will gain hands-on experience in QA processes, batch records, and regulatory readiness while contributing to continuous improvements.

The internship spans six, nine, or twelve months and emphasizes collaboration, training, and real-world exposure to quality systems. Join a team that supports patients and career growth.

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