Regulatory Affairs Specialist

1 dia atrás


São Paulo, Brasil Smith & Nephew Tempo inteiro
Regulatory Affairs Specialist (São Paulo) page is loaded## Regulatory Affairs Specialist (São Paulo)locations: Brazil - office positionstime type: Full timeposted on: Posted Todayjob requisition id: R85152**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.* 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.* 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.* 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 crafting the greatest good for society. Our strongest investments are in our people and the patients we serve.* **Inclusion and Equity-** Committed to Welcoming, Celebrating and Thriving on Diversity, Learn more about on our website.* **Your Future:** Generous annual bonus and pension Schemes, Save As You Earn share options.* **Work/Life Balance:** Flexible Vacation and Time Off, Paid Holidays and Paid Volunteering Hours, so we can give back to our communities* **Your Wellbeing:** Private Health and Dental plans, Healthcare Cash Plans, Income Protection, Life Assurance and much more.* **Flexibility**: Hybrid Working Model (For most professional roles).* **Training:** Hands-On, Team-Customized, Mentorship#LI-LATAMStay connected by joining our .We're more than just a company - we're a community Follow us on to see how we support and empower our employees and patients every day. Check us out on for a glimpse behind the scenes and a sneak peek into **You. Unlimited.**, life, culture, and benefits at S+N.Explore our and learn more about our mission, our team, and the opportunities we offer.Smith+Nephew is a global medical technology company. We design and manufacture technology that takes the limits off living. We support healthcare professionals to return their patients to health and mobility, helping them to perform at their fullest potential.From our first employee and founder, T.J. Smith, to our team today, it’s our people who make Smith+Nephew a unique place. Yes, we love to innovate and develop exciting technologies, and we offer competitive salaries and progressive benefits. But it’s our culture - of Care, Collaboration and Courage - that really sets us apart. Through a spirit of ownership and can-do attitude we work together to win. We’re a company of people who care about each other, about our customers and their patients, and about our communities. Together, we fulfill our shared purpose of Life Unlimited.
#J-18808-Ljbffr

  • São Paulo, São Paulo, Brasil UBS Tempo inteiro

    Governmental & Regulatory Affairs Specialist Join to apply for the Governmental & Regulatory Affairs Specialist role at UBS Governmental & Regulatory Affairs Specialist Join to apply for the Governmental & Regulatory Affairs Specialist role at UBS Job Reference # BRJob TypeFull TimeYour roleAre you curious, have attention to detail and the ability to...


  • São Paulo, São Paulo, Brasil Alimentiv Inc. Tempo inteiro

    Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services. Role will include management of clinical trial applications to Competent Authorities, Ethics Committees and Regulatory Agencies, and the research, review and reporting on applicable global regulations and requirements. Develop stakeholder tools,...


  • São Paulo, São Paulo, Brasil BOEING Tempo inteiro

    At Boeing, we innovate and collaborate to make the world a better place. From the seabed to outer space, you can contribute to work that matters with a company where diversity, equity and inclusion are shared values. We're committed to fostering an environment for every teammate that's welcoming, respectful and inclusive, with great opportunity for...


  • São Paulo, Brasil Insight Global Tempo inteiro

    Job Description: The position will have primary responsibility in the Global Development Information Management team. A key responsibility of this role is to identify and recommend improvements to business processes, regulatory data, and data definitions for the RIM platform, while working in close collaboration with Global Regulatory Operations (GRO),...


  • São Paulo, Brasil Smith+Nephew Tempo inteiro

    Join to apply for the Regulatory Affairs Specialist (São Paulo) role at Smith+Nephew 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...


  • Sao Paulo, Brasil Johnson & Johnson Family of Companies Tempo inteiro

    **Regulatory Affairs Senior Specialist**: At Johnson & Johnson, the largest healthcare company in the world, we come together with one purpose: to profoundly change the trajectory of health for humanity. Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1...


  • São Paulo, Brasil UBS Tempo inteiro

    Brazil - Compliance - Group Functions **Job Reference #** - 321151BR **City** - Sao Paulo **Job Type** - Full Time **Your role** - Are you curious, have attention to detail and the ability to pick up a variety of new topics quickly? You like working in a dynamic team responsible for delivering on key regulatory focus topics? We are looking for a...

  • Regulatory Affairs Expert

    2 semanas atrás


    São Paulo, Brasil beBeeRegulatory Tempo inteiro

    **Senior Regulatory Specialist Job Description** We are seeking a highly skilled and experienced Senior Regulatory Specialist to join our team. As a key member of our organization, you will be responsible for ensuring compliance with regulatory requirements and guidelines. **Key Responsibilities:** Maintain awareness of regulatory legislation, guidance, and...


  • São Paulo, São Paulo, Brasil Smith+Nephew Tempo inteiro R$80.000 - R$120.000 por ano

    Life Unlimited.At Smith+Nephew, we design and manufacture technology that takes the limits off livingAbout The RoleImagine 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...


  • São Paulo, São Paulo, Brasil buscojobs Brasil Tempo inteiro

    Quality Assurance Regulatory Affairs ManagerJob Summary:Highridge Medical creates the world's most innovative spinal solutions across the spectrum from Motion Preservation to MIS to Bone Healing to Core Spine. Working at Highridge Medical is not just work. Life at Highridge Medical is purpose driven. Every day, you have the privilege of using your talents to...