Regulatory Affairs Specialist

Regulatory Affairs Specialist Post Register - Home based - São PauloICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a...

OverviewSenior Regulatory Affairs Specialist at Monster Energy. The role focuses on registrations and compliance for raw materials and finished products, and collaboration with regulatory leaders and the regional NPD team to support product registrations and labeling in dynamic markets. The Day In The LifeAs a Sr Specialist in Regulatory Affairs, you will...

Overview Senior Regulatory Affairs Specialist at Monster Energy. The role focuses on registrations and compliance for raw materials and finished products, and collaboration with regulatory leaders and the regional NPD team to support product registrations and labeling in dynamic markets. The Day In The Life As a Sr Specialist in Regulatory Affairs, you will...

**REGULATORY AFFAIRS PROJECT MANAGEMENT SPECIALIST**: At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity. Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1...

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...

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),...

Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex international regulatory environments. Working in partnership with external government and regulatory authorities, and alongside diverse internal stakeholders, your close attention to detail...

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...

Responsible for planning and implementing the strategy for medical devices registration activities for clients - Support in responding to RFPs for regional regulatory projects - Responsible for planning, executing, and coordinating all regulatory activities including major lifecycle maintenance and customer’s market expansion activities - Able to manage...

DescriptionKenvue is currently recruiting for:**Regulatory Information Management (RIM) Specialist**This position reports into Manager, Global Reg Strategic Compliance and is based at Brazil. São Paulo Capital.**Who we are**At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the...