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At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job—you will find purpose and pride.
Baxter is seeking a highly skilled and motivated individual to join our team as a Principal Specialist in Regulatory Affairs. This is an outstanding opportunity to contribute to the success of a world-class healthcare company and make a meaningful impact on patients' lives.
As a Principal Specialist in Regulatory Affairs, with experience in EU MDR and MDD, you will work with the relevant global partners to develop and Implement regulatory strategies. You will provide support to the business to ensure/ maintain compliance with the regulations. You will also provide regulatory support/ guidance to global RA colleagues and other stakeholders within specific segments/ divisions.
What you'll be doing:
Support global regulatory and other stakeholders with regulatory activities relating to a specific portfolio of products/projects.
Act as EU Policy and Strategy Lead, managing the regulatory affairs activities for the assigned segment/ division /product portfolio
Support the development and implementation of regulatory strategies to ensure adherence to local regulations and laws
Collaborate with cross-functional teams to support vital approvals for product registrations and maintain existing licenses.
Support the preparation and submissions to regulatory bodies/ health authorities and provide support during audits and inspections.
Stay updated with the latest regulatory requirements and industry trends to provide support/ guidance and ensure flawless execution.
Provide clear communications/ training to global RA/ other stakeholders on regulatory requirements / changes related to EU MDR
Collaborate closely with regional and global regulatory teams to align strategies and exchange practical approaches.
Support the Legal Manufacturer (BHSA) in its fulfilment of its regulatory responsibilities under the MDD and MDR.
Support BHSA and other Baxter legal manufacturers in CE mark related regulatory activities in front of the Notified Bodies and relevant Competent Authorities.
What you'll bring:
Degree in a relevant scientific field
Experienced specialist in Regulatory affairs within the EU MDR and MDD.
Proven track record of successfully implementing regulatory strategies and acquiring product registrations
Solid understanding of regulatory requirements and processes related to CE marking of medical devices
Excellent communication and interpersonal skills
Experienced using systems such as Trackwise / TCU document control / RIM Vault
Ability to work independently and collaborate effectively in a cross-functional team environment
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Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
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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