Regulatory Affairs Intern: Cross-Functional Pharma Experience

Regulatory Jobs; Indianapolis (IN); Vor Ort; USD 33.000 - 62.000; Vollzeit

Zusammenfassung

Bristol Myers Squibb offers a full-time Regulatory Affairs Intern position in Indianapolis, June–August 2027. You will support the Regulatory Affairs team with document preparation, submission tracking, and cross-functional coordination.

The role provides hands-on regulatory exposure within a pharmaceutical setting, building skills in documentation, project management, and regulatory compliance.

Qualifikationen

• Currently pursuing a Bachelor’s degree in Life Sciences, Pharmacy, Public Health, or related field.
• Strong interest in regulatory affairs and drug development.
• Excellent organizational and communication skills.

Aufgaben

• Regulatory documentation support and formatting of submissions.
• Maintain submission trackers and document repositories.
• Review documents for consistency and completeness under supervision.
• Coordinate with cross-functional teams on timelines and tasks.
• Attend meetings and record action items and follow-ups.
• Draft internal regulatory summaries and communications.
• Shadow cross-functional meetings to understand regulatory integration.
• Conduct literature reviews and regulatory intelligence gathering.
• Summarize relevant FDA/EMA guidance documents.
• Monitor regulatory changes and flag updates to the team.

Kenntnisse

Strong regulatory interest

Excellent organizational skills

Strong written and verbal skills

Ausbildung

Bachelor’s degree in Life Sciences/Pharmacy/Public Health or related field

Tools

MS Word

MS Excel

PowerPoint

Outlook

Adobe Acrobat

Smartsheet

MS Project

Jobbeschreibung

Bristol Myers Squibb offers a full-time Regulatory Affairs Intern position in Indianapolis, June–August 2027. You will support the Regulatory Affairs team with document preparation, submission tracking, and cross-functional coordination.

The role provides hands-on regulatory exposure within a pharmaceutical setting, building skills in documentation, project management, and regulatory compliance.