Quality Operations Intern – GMP, CAPA & RCA

Bristol Myers Squibb UK & Ireland

Dublin

Vor Ort

EUR 19.000 - 22.000

Vollzeit

vor 10 Stunden
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Bristol Myers Squibb UK & Ireland is offering an internship program across a team of Quality Professionals that provide support to CMOs and BMS groups. You will gain hands-on experience in investigations, CAPAs, change controls and documentation while collaborating with Supply Chain, Regulatory and MS&T teams.

The role emphasizes learning GMP basics, data handling in Excel/PowerPoint, and contributing to annual product reviews.

Qualifikationen

  • Minimum 2 years of relevant academic experience and knowledge in a science discipline.
  • Strong communication and teamwork abilities in cross-functional settings.
  • Good technical writing skills and understanding of GMP.
  • Proficiency with MS Excel and PowerPoint; strong organizational skills.

Aufgaben

  • Support investigations and responses to market product complaints.
  • Assist investigations from manufacture and packaging (RCA, CAPAs).
  • Assist change controls including impact assessments.
  • Review batch documentation and Regulatory Restriction Forms.
  • Coordinate quality metrics programs.
  • Assist preparation of Annual Product Reviews for products.
  • Support improvement projects and answer queries related to manufacturing.
  • Collaborate with Quality, Supply chain, Regulatory, MS&T and systems teams.

Kenntnisse

Communication skills
Cross-functional teamwork
Technical writing
MS Excel
PowerPoint
Organizational skills
Multitasking
Computerized systems
Travel

Ausbildung

Two years relevant academic experience in science

Tools

MS Excel
PowerPoint

Jobbeschreibung

Bristol Myers Squibb UK & Ireland is offering an internship program across a team of Quality Professionals that provide support to CMOs and BMS groups. You will gain hands-on experience in investigations, CAPAs, change controls and documentation while collaborating with Supply Chain, Regulatory and MS&T teams.

The role emphasizes learning GMP basics, data handling in Excel/PowerPoint, and contributing to annual product reviews.

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