At a Glance
- Tasks: Lead EU regulatory strategies for biologics and manage operations in a global setting.
- Company: Join a leading global CDMO with a focus on innovation and collaboration.
- Benefits: Remote work, competitive salary, and opportunities for professional growth.
- Other info: Flexible remote role with travel opportunities to enhance your career.
- Why this job: Make a significant impact in the biologics field while working from anywhere in the UK.
- Qualifications: 15+ years in regulatory affairs with expertise in biologics and leadership skills.
The predicted salary is between 80000 - 100000 £ per year.
Blackfield Associates is seeking a Regulatory Affairs Director to enhance EU regulatory capabilities within a global CDMO. This role involves providing strategic guidance and managing regulatory operations for large molecule drug substances and biologics.
The ideal candidate will have 15+ years of regulatory affairs experience, a strong background in biologics development, and proven leadership in matrix environments.
This full-time, permanent role is remote-based in the UK, requiring travel (~30%).
EU Regulatory Affairs Director: Biologics employer: Blackfield Associates
At Blackfield Associates, we pride ourselves on being an exceptional employer, particularly for the role of Plant Quality Manager in Folkestone. Our commitment to fostering a collaborative work culture is complemented by robust employee growth opportunities and a focus on continuous improvement, ensuring that our team members thrive both personally and professionally. With a strong emphasis on quality and regulatory compliance, we offer a dynamic environment where your expertise will be valued and your contributions will directly impact our success.
