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Sr Spec Regulatory Affairs México
hace 4 meses
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.
About Us: Baxter's Mission
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.
Your Role at Baxter
THIS IS WHERE you build trust to achieve results
As a Sr Spec Regulatory Affairs you support the development of business strategies for compliance with registration plans, ensure the obtaining and maintenance of product registrations and local certifications for imported products for the Business Units, provide regulatory support to the company and participate in the optimization of the improvement processes. Our customers trust you and appreciate your knowledge and curiosity when finding solutions to meet their needs.
What you'll be doing:
Support the LATAM regulatory affairs team in obtaining legal documents such FSC, CFGs and ISO from the legacy Hillrom manufacturing plants globally. Participation and support in the implementation of regional and global projects of the regulatory function in LATAM. Assist the legacy Hillrom Operations Department about documents and processes needed for customers purchase orders and importations. Keep updated the importations licenses for Mexico. Coordination and support for the Inmetro and B-GMP audits at the manufacturing sites.
What you'll bring:
Bachelor's degree with 3+ years of relevant experience LATAM regulations and local Certification processes. Candidate must possess strong interpersonal and communication skills, both written and oral, strong presentation skills