Global Labeling Strategist - Contract - #1673516

AL Solutions


Date: 8 hours ago
City: Edinburgh
Contract type: Full time
Work schedule: Full day
AL Solutions

A leading life sciences company is seeking a Global Labeling Strategist to join its international Regulatory Affairs team. This position offers the opportunity to shape and manage global labeling strategies across a diverse portfolio, working with regulatory documentation such as the Company Core Data Sheet (CCDS), US Package Inserts (USPI), and EU Summary of Product Characteristics (SmPC).


This is a fully remote role, ideal for professionals looking to make a strategic impact in regulatory labeling across global markets.


Key Responsibilities:



  • Develop and drive global labeling strategies in alignment with regulatory and product objectives.

  • Manage updates and compliance of CCDS, USPI, and SmPC for products registered via Centralized, Mutual Recognition, or Decentralized Procedures.

  • Serve as the primary point of contact for the Labeling Strategy Team (LST).

  • Collaborate closely with cross-functional teams including Regulatory, Clinical, Medical, and Safety functions to ensure timely and compliant label updates.

  • Coordinate and oversee end-to-end labeling activities and submission planning.

  • Support responses to health authority inquiries and inspection-related labeling issues.

  • Review country-specific labels to ensure accuracy and global consistency.


Candidate Requirements:



  • Experience in regulatory labeling for at least one major market (e.g., US, EU).

  • Solid understanding of global regulatory procedures, GxP requirements, and lifecycle management.

  • Hands-on experience managing CCDS, SmPC, and USPI development and updates.

  • Strong project management skills with experience in coordinating cross-functional teams.

  • Excellent verbal and written communication abilities.

  • Attention to detail and a thorough understanding of clinical and scientific documentation.


Desirable Skills:



  • Experience with global health authority submissions and queries.

  • Ability to influence and guide internal stakeholders and subject matter experts.

  • Familiarity with centralized and decentralized product registration processes.

  • Prior experience working in a matrixed or global team environment.

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