Regulatory Affairs Specialist (São Paulo) job opportunity at Smith+Nephew.

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Smith+Nephew Regulatory Affairs Specialist (São Paulo)
Experience: 3-years
Pattern: full-time
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loacation Brazil - office positions, Brazil
loacation Brazil - offic..........Brazil

Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living! About the role Imagine a role where you're not just part of the process, you redefine it. At the heart of our innovative medical devices' company, we’re looking for a trailblazer to join our Regulatory Operations team in Brazil. This isn’t your typical regulatory role. Experience in the medical devices, responsible for registration, certification,  and regulatory maintenance of medical devices across different risk classes (I to IV), with focus on regulatory compliance in Brazil and other Latin American countries. What Will You Be Doing? Key responsibilities include managing certification processes with regulatory bodies such as ANVISA, INMETRO and ANATEL; preparing, reviewing, and submitting registration dossiers; obtaining Good Manufacturing Practices (GMP) certifications; and ensuring compliance with local and regional requirements. This professional will participate in regional regulatory projects, keep regulatory databases and product registrations up to date, and handle renewals, amendments, and maintenance of registrations. The role requires direct interaction with distributors, regulatory consultants, and health authorities, as well as continuous monitoring of regulatory changes across LATAM countries. The position also provides technical-regulatory support to internal departments such as Quality, Commercial, and Operations, and involves participation in internal and external audits. What will you need to be successful? Requirements include a university degree in Pharmacy, Biomedical Engineering, Biomedicine, or related fields; proven experience in regulatory affairs for medical devices; product registration expertise; knowledge of INMETRO, ANATEL, and GMP certifications; and preferably experience with LATAM regulations. Experience: At least 3 years of proven experience in regulatory affairs for medical devices . Fluent English, communication skills, organizational ability, and collaborative work style. Preferred qualifications: postgraduate degree or specialization in Regulatory Affairs, and intermediate to advanced Spanish. You. Unlimited. We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.    Inclusion+belonging :   Committed to Welcoming, Celebrating and Thriving, learn more about employee inclusion groups on   our   website   Other reasons why you will love it here!   •   Your savings:   food, meal, and transportation vouchers   • Your well-being:   legal, psychological, and financial   assistance , access to   Wellhub   and   Totalpass , life insurance, private pension plan, Care Plus , profit   sharing.   •   Flexibility : flexible hours, possibility of remote work depending on the role.   • Learning:   unlimited access to learning tools.   #LI-HYBRID Stay connected by joining our Talent Community . We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day.    Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You. Unlimited. , life, culture, and benefits at S+N. Explore our website and learn more about our mission, our team, and the opportunities we offer.  

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