GRS Manager (Regulatory Affairs Manager)
Bristol Myers Squibb · Buenos Aires, AR
RegulatoryFull-timeCompany career page
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Role summary
Bristol Myers Squibb seeks a Regulatory Affairs Manager in Buenos Aires to oversee pharmaceutical regulatory submissions, compliance, and product lifecycle management. The role involves collaborating on new drug registrations, managing health authority interactions, and ensuring adherence to regulatory requirements while supporting commercial objectives.
What they're looking for
- Science-related degree
- More than 7 years pharma industry experience
- Fluent English proficiency
- Up-to-date regulatory knowledge and new drug development experience
- Strong communication and interpersonal skills
- Team leadership and strategic agility capabilities
What you'll be doing
- Collaborate on regulatory strategy for new product registrations and lifecycle management aligned with business goals
- Prepare, submit, and track new license applications and post-approval variations
- Manage health authority requisitions and communicate submission status to relevant parties
- Review and approve promotional materials in compliance with regulations
- Maintain relationships with functional areas including Medical, Supply, Commercial, and QA/QC
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.