Global Labeling Lead

Freyr Solutions; Norwich; On-site; GBP 90,000 - 130,000; Full time

Job summary

Freyr is seeking a Global Labeling Lead for a 10–12 month fixed-term role across multiple regions including the UK, Poland, and other European markets. The candidate will develop and implement labeling strategies, coordinate with global teams, and ensure compliance with health authority expectations.

The role requires extensive labeling experience, strategic regulatory thinking, and strong communication skills to lead cross-functional efforts and inspections across international markets.

Qualifications

• 8+ years in pharmaceutical industry with labeling experience.
• Ability to develop regulatory strategies based on regulatory requirements and risks.
• Strong communication across global cross-functional teams.
• Excellent written and verbal communication skills.

Responsibilities

• Escalates issues to Global Labeling management and proposes risk mitigation strategies.
• Develops and maintains relationships across labeling cross-functional teams to ensure effective communication.
• Conducts precedent searches and analyzes competitor labeling to inform labeling strategy and language.
• Represents Global Labeling at Global Regulatory Team and coordinates with US/EU operations and Labeling Devices/Compliance teams.
• Supports Health Authority inspections by providing labeling information requests related to products and labeling processes.
• Oversees labeling activities managed by external vendors to ensure timely delivery and adherence to quality standards.
• Contributes to continuous improvement of labeling processes for agility, efficiency and accuracy.

Skills

Pharmaceutical labeling experience

Strategic regulatory thinking

Cross-functional collaboration

Excellent communication skills

Education

BSc degree

MSc/PhD/PharmD preferred

Job description

About Freyr

Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. We partner with leading pharmaceutical, biotechnology, and medical device companies, delivering end-to-end regulatory operations support and regulatory strategy with precision, speed, and global expertise.

This is a 10 ~ 12 month fixed term role

Job Title: Global Labeling Lead

Location : Poland, UK , Romania, Hungary, Croatia, Czech Republic

Job Description

• Appropriately escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned products following global labeling communication guidance and proposes risk mitigation.
• Strategically develop and cultivate strong relationships among functions represented at the Labeling cross functional teams including clinical, safety, medical affairs, and commercial, to ensure the highest level of communication effectiveness for labeling strategy and content.
• Precedent Search and Labeling Trends - Conducts precedent, analyzes relevant competitor labeling, health authority labeling requests for Client products, labeling guidance and trends; and develops strategies and labeling language for assigned product labels (TLP, CCDS, USPI, EU SmPC, others as appropriate) to ensure consistency with the overall product strategy, product claims and information in the CCDS and to ensure that Client products have the most competitive labeling possible; while maintaining awareness of recent in-class approvals.
• Working within Labeling Team and GRA - Represents Global Labeling at Global Regulatory Team (GRT) - Liaises with US Labeling Operations, EU Labeling Operations, Labeling Devices Lead and Labeling Compliance to ensure labeling objectives and timelines are met.
• Represents global labeling in departmental and cross-functional task-forces and initiatives.
• Supports Health Authority Inspections (US, EU, and Global) by providing labeling information requests related to assigned products and overall labeling processes.
• Vendor Management - Oversight and accountability for labeling activities managed by external vendor(s) for assigned products, ensuring seamless coordination, timely delivery, and adherence to quality standards.
• Continuous Improvement - Actively contributes to the continuous improvement of labeling processes, identifying opportunities for optimization and implementing effective strategies to enhance agility, efficiency and accuracy.

Education & Competencies (Technical and Behavioral)

• BSc degree, preferred; BA accepted.
• Advanced scientific degree (MSc, PhD, or PharmD) preferred.
• 8+ years of pharmaceutical industry experience. This is inclusive of 6 years of labeling experience or combination of 5+ years regulatory and/or related experience.
• Strategic Thinking - Ability to develop & execute clear and practical regulatory strategies based on regulatory requirements, competitive landscape, key priorities and risk management.
• Demonstrates an understanding of core business aspect.
• Communication - Ability to effectively collaborate with global cross-functional teams.
• Ability to use communication skills to transfer knowledge, convey complex regulatory information in a clear and concise manner in written, verbal and group presentation formats.
• Ability to promote regulatory decisions across global cross-functional teams.