Regulatory Affairs Manager Greece Cyprus Malta
Job Summary
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About the Role
As the Regulatory Affairs Manager you will be responsible for ensuring compliant and timely regulatory lifecycle management of Takedas product portfolio across Greece Cyprus and Malta. You will act as the key regulatory contact for local Health Authorities and Global Regulatory Affairs supporting product registrations lifecycle activities labelling compliance and regulatory strategy to ensure continued market access. Working cross-functionally you will help deliver high-quality regulatory execution while supporting Takedas commercial objectives and commitment to patients.
How You Will Contribute
Lead regulatory lifecycle management activities including new registrations renewals variations PSUR/PBRERs and national regulatory procedures.
Manage national phases of European procedures and ensure timely regulatory submissions approvals and maintenance activities across Greece Cyprus and Malta.
Assess the local impact of global dossier updates and coordinate implementation through established change control processes.
Ensure product information labelling artworks and mock-ups remain compliant with EU local and global regulatory requirements.
Coordinate the preparation review approval and distribution of local regulatory translations and affiliate feedback.
Build and maintain effective relationships with local Health Authorities while serving as the primary regulatory liaison with Global Regulatory Affairs.
Support regulatory compliance during audits and inspections while proactively identifying regulatory risks and process improvement opportunities.
Provide regulatory expertise to cross-functional teams including participation in MLR reviews and support for product launches and commercial initiatives.
What You Bring to Takeda
Bachelors degree in Life Sciences or another relevant scientific discipline.
Minimum of 3 years Regulatory Affairs experience ideally within a multinational pharmaceutical environment.
- Strong knowledge of EU and local Regulatory Affairs requirements including lifecycle management and marketing authorization procedures.
- Experience of reviewing promotional/medical material based on local legislation requirements
Experience interacting with Health Authorities and managing regulatory submissions across multiple products.
Understanding of regulatory change control processes product information and labelling requirements.
Experience working effectively within cross-functional and international teams.
Excellent planning organizational analytical and problem-solving skills with strong attention to detail.
Fluent written and spoken Greek and English with excellent communication and stakeholder management skills.
Base Salary Range:
49200.00 - 67650.00For information about our benefits please click here.
Required Experience:
Manager
About Company
Takeda is a patient-focused, R&D-driven global biopharmaceutical company committed to bringing Better Health and a Brighter Future.