Regulatory Strategy Manager – Hybrid Pharma

Bristol-Myers Squibb Co; Buenos Aires; Híbrido; ARS 2.400.000 - 3.600.000; Jornada completa

Descripción de la vacante

Bristol Myers Squibb Co is seeking a Regulatory Affairs Manager to strengthen our regulatory strategy for new product registrations and lifecycle management. This role will coordinate with country teams to ensure timely submissions and compliance across medical, supply, and commercial functions.

The ideal candidate has extensive pharma regulatory experience, fluent English, and strong communication skills. This position supports a hybrid/work model aligned with core responsibilities and company

Formación

• Science related degree.
• Fluent English skills.
• Excellent technology profile.
• Transparent communication.

Responsabilidades

• Collaborate with country regulatory strategy for new products registration and life cycle management in alignment with business goals.
• Communicate regulatory submission dates, regulatory status, nature of changes, track and inform of minor/significant product information changes to all relevant parties.
• Maintain strong relationships with other functional areas (i.e., Medical, Supply, Commercial, QA/QC).
• Plan and track activities related to regulatory submissions.
• Plan, prepare, submit and follow up new license applications and post approval variations (labeling, CMC).
• Responsible for the in-time review and approval of 100% promotional materials.
• Management of Health Authority (HA) requisitions.
• Identify opportunities to improve departmental functions/processes

Conocimientos

Fluent English

Transparent communication

Tech-savvy

Educación

Science related degree

Descripción del empleo

Bristol Myers Squibb Co is seeking a Regulatory Affairs Manager to strengthen our regulatory strategy for new product registrations and lifecycle management. This role will coordinate with country teams to ensure timely submissions and compliance across medical, supply, and commercial functions.

The ideal candidate has extensive pharma regulatory experience, fluent English, and strong communication skills. This position supports a hybrid/work model aligned with core responsibilities and company