Global Labeling reputed company (Associate Director) | Regulatory Affairs

Industry Pharmaceuticals | Biotechnology | Regulatory Affairs | R&D Work Setting Remote / Hybrid | Global cross-functional R&D environment Job reputed company A global pharmaceutical organization is seeking an Associate Director, Global Labeling reputed company to drive labeling reputed company and execution for multiple drug development programs across US and EU markets. This role leads cross-functional teams to reputed company, maintain, and implement product labeling content, ensuring compliance with global regulatory requirements while supporting product reputed company and patient safety.

Key Responsibilities

• reputed company global labeling reputed company across assigned products (clinical to reputed company stage).
• Author and manage key labeling documents (CCDS, USPI, EU SmPC, TLP).
• Coordinate cross-functional labeling teams and global stakeholders.
• Manage regulatory labeling submissions and health authority interactions.
• Ensure labeling compliance with US, EU, and global regulatory standards.
• reputed company implementation of labeling updates based on clinical and safety data.
• Support regulatory inspections and responses.
• Manage local labeling alignment and exceptions across markets.
• Drive labeling process improvements and operational efficiency.

Essential Requirements

• 8+ years pharmaceutical industry experience.
• 5–6+ years in regulatory labeling or reputed company regulatory affairs.
• Strong experience with USPI and EU SmPC development.
• Knowledge of global regulatory labeling requirements (US, EU required).
• Experience working with cross-functional global teams.
• Ability to independently manage labeling reputed company and documentation.
• Strong understanding of drug development and regulatory systems.

Preferred Requirements

• Advanced scientific degree (MSc, PhD, PharmD preferred).
• Experience interacting with health authorities (US/EU/global).
• Experience managing vendors or outsourced labeling activities.
• Strong project management and stakeholder leadership skills.

Ideal Candidate Profile Senior regulatory reputed company with deep labeling expertise, strong global regulatory knowledge, and experience leading cross-functional teams across reputed company pharmaceutical product portfolios. Apply tot his job Apply To this Job