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Job DescriptionAbout 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.
Base Salary Range:
€49,200.00 - €67,650.00The 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 TypeEmployeeWorker Sub-TypeRegularTime TypeFull timeSkills Required
- Bachelor's degree in Life Sciences or another relevant scientific discipline
- Minimum of 3 years of Regulatory Affairs experience
- Experience ideally within a multinational pharmaceutical environment
- Strong knowledge of EU and local Regulatory Affairs requirements
- Knowledge of lifecycle management and marketing authorization procedures
- Experience reviewing promotional and medical materials under local legislation
- Experience interacting with Health Authorities
- Experience managing regulatory submissions across multiple products
- Understanding of regulatory change control processes, product information, and labeling requirements
- Experience working effectively within cross-functional and international teams
- Excellent planning, organizational, analytical, and problem-solving skills
- Strong attention to detail
- Fluent written and spoken Greek and English
- Excellent communication and stakeholder management skills
Takeda Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Takeda and has not been reviewed or approved by Takeda.
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Retirement Support — Employer-funded retirement is described as notably strong, combining a dollar-for-dollar 401(k) match with an additional company contribution that scales with age and service. Access to an employee stock purchase plan further supports long-term wealth building.
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Parental & Family Support — Paid bonding leave for all parents, substantial adoption/surrogacy reimbursement, and robust caregiver resources (backup care and Maven family-forming support) are emphasized as core strengths. These offerings create a comprehensive safety net for a range of family situations.
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Healthcare Strength — Multiple medical plan options (nationwide PPO/HSA and regional HMOs), employer HSA funding, and integrated mental-health and well-being programs signal depth in coverage. Preventive care is covered in-network, and plan choices by state expand access.
Takeda Insights
What We Do
For over 240 years, Takeda’s propensity to evolve has driven the next generation of innovation, and as a future-focused organization, we’re continuing to drive forward with endurance in our steadfast pursuit to achieve the best outcomes for our patients in a rapidly changing world. We have been preparing for this period of value creation by investing in data, digital and technology, and we’re proud of our employees and their commitment to turning groundbreaking ideas into life-changing impacts. Since our founding in Japan, integrity and putting patients first have been at the heart of our identity, and we will emerge ready for our future as one of the most trusted and science-driven digital biopharmaceutical companies. Join a team where your innovation impacts lives. Together, we’ll realize improved outcomes by improving data quality, enhancing launch execution and improving the patient journey. You’ll play a critical role in accelerating data collection and increasing accuracy across all parts of the business. Patients across the globe will benefit from access to treatments afforded by greater opportunities and efficiency in our research and development.
Why Work With Us
We connect to our history and Japanese heritage through everything we do to bring our purpose, values, vision, and imperatives to life. We are committed to bringing better health and a brighter future to patients. Being a part of Takeda means having the opportunity to be a part of something bigger than yourself.
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