Sr. Regulatory Affairs Specialist

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Your Role at Baxter:

We have a wonderful opportunity for a Senior Regulatory Affairs Specialist at our office in Athens, Greece. You will be responsible for managing national regulatory approvals of medicinal products and establishing appropriate contact with the Regulatory Authorities. You will ensure that regulatory compliance is maintained for our products/services and will act according to the country policies and practices to reduce Baxter's exposure to regulatory, quality and liability risks.

If you are passionate about regulatory affairs and looking for a place where you choose to work with talented and dynamic people whose primary focus is to save and sustain lives and your work values focus on speed, simplicity, courage and collaboration. Then we would love to hear from you.

What are your responsibilities?

• Support the Regulatory Affairs department with all general tasks
• Responsible for the implementation of complex regulatory strategies, obtain and maintain marketing authorizations for pharmaceutical product(s) and communication of general regulatory requirements in support of licensing of Baxter’s products.
• Maintenance of drugs licenses: variations, labeling, renewals
• Review and translate IFUs and labeling of pharma and medical devices products
• Maintenance, updates and creation of medical devices in the database
• Maintenance, updates and creation of medical devices in our systems
• Labelling and Manual translations for pharma and medical devices products
• Review promotional material and manage safety information material

We are presently seeking people who have:

• Bachelor´s degree in life sciences required. (Biology, Pharmacy)
• Experience working in the Department of Registration in the area of health products, pharmaceutical drugs and medical devices
• An eye for details and the ability to work under pressure
• European and national knowledge of medicinal and health product regulations
• Fluency in English and Greek

Why do you want to work at Baxter?

• Competitive total compensation package
• Professional development opportunities
• High importance placed on work life balance
• Commitment to growing and developing an inclusive and diverse workforce

Equal Employment Opportunity

Baxter is an equal opportunity employer and is therefore firmly committed towards making employment opportunities available to all qualified applicants without regard to gender, race, age, disability, colour, nationality, ethnic or national origin, marital status, sexual orientation, responsibility for dependents, religion or trade union membership.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

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