Quality Compliance - Regulatory Operations Intern
Bristol Myers Squibb · Dublin, Ireland
RegulatoryFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Bristol Myers Squibb seeks an intern to support quality compliance and regulatory operations across external manufacturing in Dublin. The role involves participating in quality activities, managing regulatory documentation, and assisting with compliance initiatives within a cross-functional environment.
What they're looking for
- Currently enrolled in undergraduate degree in science-related field (biomedical sciences, biotechnology, pharmaceutical chemistry, or similar)
- Strong organizational and time management skills with ability to handle multiple tasks independently
- Effective communication, interpersonal, and teamwork abilities
- Proficiency with Microsoft Office applications (Word, Excel, Access, PowerPoint)
- Demonstrated capacity to work in fast-paced environment managing concurrent projects
- Confident public speaking and stakeholder engagement skills
- Interest in pharmaceutical sector and healthcare innovation
What you'll be doing
- Support compilation and tracking of quality and regulatory performance metrics across external manufacturing
- Assist with regulatory restriction forms, filing applications, and regulatory requests as applicable
- Collaborate with virtual plant teams on change controls, deviations, CAPAs, complaints, audits, and inspections
- Support preparation of regulatory summaries for annual product quality reports
- Assist with GMP and regulatory document progression and review within documentation management systems
Compensation€2,213.90 per month
Privacy & handoff
This role links to Bristol Myers Squibb's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.