Regulatory Affairs Specialist

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...

**_Purpose_** - The Specialist, Regulatory Affairs Submission Management, manages simple to moderately complex submission projects involving multiple cross-functional regulatory submission teams. With input from the submission teams and their supervisor, the Specialist establishes and maintains submission planners and associated timelines, facilitates...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Sewell Lincoln. This role will be responsible for coordinating and submitting new drug / medical devices applications to regulatory agencies in Brazil.Key Responsibilities:Plan, conduct and coordinate JJV regulatory activities for Brazil, ensuring compliance with...

**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...

Job OverviewCatho Online Ltda. - Br - Specialist is seeking a highly skilled Regulatory Affairs Specialist to join their team. This role involves ensuring compliance with Brazilian regulations and facilitating the registration of medical devices.Estimated Salary: R$ 8,500 - R$ 12,000 per month, depending on experience.Key Responsibilities:Submit registration...

Sully's Steamers Johnson City seeks a highly skilled Regulatory Affairs Specialist to coordinate, compile and submit new drug/medical devices applications to regulatory agencies in Brazil.The ideal candidate will plan, conduct and coordinate JJV regulatory activities for Brazil, working closely with RA management to establish and execute regulatory...

**Job Description**: **SUMMARY** The Associate Specialist, Regulatory Affairs supports a variety of regulatory and cross-functional initiatives and executes/ tracks all activities associated to different types of regulatory submissions and products, in collaboration with internal and external stakeholders, following global and local strategies and oriented...

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...

Description Kenvue 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,...

**REGULATORY AFFAIRS SR SPECIALIST - LATAM** 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 billion...

**Unilever is currently hiring for a Regulatory Affairs Manager based in São Paulo.** **Unilever** is the place where you can bring your purpose to life with the work that you do - creating a better business and a better world. We are looking for talents that would like to join this exciting journey with us. Our **R&D Brazil Beauty & Wellbeing** team is...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role involves strategic intelligence and guidance, ensuring that client...

At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the globe. Our...

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...

We are searching for the best talent for REGULATORY AFFAIRS ANALYST to be in São Paulo/Brazil. You will be responsible for: - In partnership with the LATAM RA PMO executes registration strategies for designated regional projects related to new/existing products, according to local regulation, approved licenses, and RA Hub/Country alignment; - Adheres to...

**Skills and knowledge**: Regulatory Affairs Consultant should have solid local expertise in submitting Clinical Trials to Health Authority in Brazil. This role will be responsible for managing and coordinating the regulatory submission strategy for a large number of clinical trials in Brazil. Also, will coordinate and manage flow of information, track...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Sully's Steamers Johnson City. This role will be responsible for coordinating, compiling, and submitting new drug/medical devices applications to regulatory agencies in Brazil.Main Responsibilities:Coordinate Regulatory Activities: Plan, conduct, and coordinate JJV...

**Responsabilidades e atribuições** - Coordinate and request technical information (GMO, Prop 65, Etc.) from suppliers - Create/maintain product specifications for ingredients, resale and manufactured products - Backup for ticket assignment/triage. - Maintenance of Portal documentation/connections - Maintain SpecSafe contacts - Other tasks as...

Job title: Regulatory Affairs Team Manager - Vaga Exclusiva Para Pessoas com Deficiencia (PcD) Location: São Paulo/SP About the jobRegulatory Affairs team in Brazil is part of a single digitally savvy and agile regulatory community effectively partnering with our diverse business units and platforms by building constructive relationships with Health...