Director - CMC

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.

The Director CMC Liaison connects global Regulatory CMC teams with local affiliates, driving regional alignment and efficiency in post-approval submissions. This role supports a diverse product portfolio—including small molecules and biologics, ensuring development of regional regulatory strategies in assigned markets, but also development of submission packages and their distribution with a regionalized approach. This role is instrumental in driving efficiency and consistency across countries within the region by leveraging regional strategies and aligning with global submission plans.

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• Act as the primary point of contact between global Regulatory CMC and local affiliates for submission package preparation and delivery.
  
• Translate global CMC strategies into actionable regional plans, ensuring alignment with country-specific requirements.
  
• Oversee the preparation, review, and submission of regulatory dossiers across the region.
  
• Develop and implement regional submission strategies to streamline processes and reduce duplication of effort.
  
• Partner with affiliates to identify opportunities for harmonization across the region.
  
• Build strong relationships with local affiliates to understand country-specific regulatory needs and challenges.
  
• Liaise with global Regulatory CMC teams to provide regional insights and feedback.
  
• Identify bottlenecks in the regional submission process and propose innovative solutions to enhance efficiency.
  
• Monitor and report on submission timelines and regulatory approvals across the region.
  
• Lead or support the development of regional strategies, training, and capability‑building initiatives to strengthen the Regional CMC regulatory network.
  

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• BS/BA Degree in a Scientific Discipline, Advanced Degree (M.S., Ph.D., etc.) preferred.
  
• 10+ years of overall biopharmaceutical/device industry experience with 8+ years of relevant pharmaceutical Regulatory CMC or Device experience, including experience leading a major variation/amendment, supporting an initial IND/IMPD preparation, or supporting an initial NDA/BLA. Equivalent industry experience in Pharmaceutical Development, Analytical Development, Production, Quality Assurance can be considered.
  
• Understanding of scientific principles and regulatory CMC requirements relevant to global drug development and post‑market support.
  
• Strong practical experience with global HA requirements, beyond EU/US.
  
• Proven ability to understand and communicate regulatory strategy to drug development, registration, and post‑market support teams.
  
• Analyze issues with attention to detail.
  
• Ability to assess alternative approaches.
  
• Proven ability to develop global regulatory strategy recommendations based on precedents and other regulatory intelligence as well as regulations and guidelines.
  
• Able to deal with issues of critical importance with minimal oversight. Exercises good judgment in elevating and communicating actual or potential issues to line management.
  
• Understand who is responsible for different decisions and escalates as necessary.
  
• Applies directions taken by the company.
  
• Demonstrates emerging leadership, problem‑solving ability, flexibility and values teamwork.
  
• Intentionally promotes an inclusive culture.
  
• Applies given prioritization framework with limited support.
  
• Excellent written and oral communication skills required. xcfaprz
  
• Excellent skills in leadership, collaboration, negotiation, problem solving, and fostering interpersonal connections through teamwork.