Regulatory Affairs Manager Greece Cyprus Malta

takeda· GRC - 8086 Takeda Hellas Pharmaceutical S.A
Apply Now ↗
📍 Athens, GreeceFull time💰 EUR 49K–68K

About this role

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use.  I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

About the Role

As the Regulatory Affairs Manager, you will be responsible for ensuring compliant and timely regulatory lifecycle management of Takeda's 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 Takeda's 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

  • Bachelor's 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.

Locations

Athens, Greece

Base Salary Range:

€49,200.00 - €67,650.00


The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.


For information about our benefits, please click here.

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Frequently Asked Questions

What is the salary for the Regulatory Affairs Manager Greece Cyprus Malta role at takeda?
The listed salary for this Regulatory Affairs Manager Greece Cyprus Malta position at takeda is EUR 49K–68K. This is an Full time role.
Where is the Regulatory Affairs Manager Greece Cyprus Malta position at takeda located?
This Regulatory Affairs Manager Greece Cyprus Malta role at takeda is based in Athens, Greece. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Regulatory Affairs Manager Greece Cyprus Malta role at takeda full-time or part-time?
This is listed as a Full time position. It is posted as a Regulatory Affairs Manager Greece Cyprus Malta role in the GRC - 8086 Takeda Hellas Pharmaceutical S.A department at takeda.
Which team or department does the Regulatory Affairs Manager Greece Cyprus Malta at takeda belong to?
This Regulatory Affairs Manager Greece Cyprus Malta position is part of the GRC - 8086 Takeda Hellas Pharmaceutical S.A department at takeda. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Regulatory Affairs Manager Greece Cyprus Malta position at takeda?
Click the "Apply Now" button on this page. You will be redirected to takeda's official application portal hosted on workday where you can submit your application directly.
When was the Regulatory Affairs Manager Greece Cyprus Malta job at takeda posted?
This Regulatory Affairs Manager Greece Cyprus Malta position at takeda was posted on Sep 15, 2026. Apply as soon as possible — early applications are often reviewed first.
Regulatory Affairs Manager Greece Cyprus Malta
takeda · 💰 EUR 49K–68K
Apply for this role ↗

You'll be redirected to takeda's official application page on Workday.