Assoc. Scientist, Regulatory Affairs

**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...

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...

Tether Operations Limited is a pioneer in the financial industry, committed to innovation and technological advancement. We are seeking an experienced Regulatory Affairs Director to join our team.This role offers a unique opportunity to shape the regulatory landscape of the industry and contribute to the growth of our company.

Job title:Regulatory Affairs Team Manager - Vaga Exclusiva Para Pessoas com Deficiencia (PcD)Location:São Paulo/SPAbout 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 Authorities...

**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...

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 Manager Quality Compliance Quality Compliance is a company of excellence in Life Sciences and one of the largest employers in the Brazilian pharmaceutical sector. We offer opportunities for you to join and grow in your career, which is we are always looking for new talents to join our team and our clientes for contribute to improving the...

OverviewCatho Online Ltda. is seeking a skilled Regulatory Affairs Team Manager to join our team in São Paulo, Brazil.This is an exciting opportunity for a seasoned professional to lead our regulatory affairs team and contribute to the growth and success of our organization.

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...

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...

**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 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...

**Role Summary**We are seeking a highly skilled Regulatory Affairs Director to lead our Regulatory Affairs team in Brazil. The successful candidate will be responsible for designing and implementing the strategic vision for the Regulatory Affairs department in Brazil, ensuring successful execution in line with company objectives.Key Responsibilities:Sets up...

**Why Join Us?** - Be a hero for our rare disease patients_ Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth - so employees can thrive in all areas of their lives, in and outside...

**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...

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...

Givaudan is a world leader in the creation of fragrances and flavors. As a Regulatory Affairs Documentation Lead, you will be responsible for leading our fragrance and beauty regulatory documentation team to ensure compliance with industry regulations.**Job Summary:**The successful candidate will have a strong background in regulatory affairs, excellent...

Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest...

As a Senior Regulatory Affairs Associate you will have the opportunity to work within Regulatory Authority Submissions related to Clinical Trials, supporting many projects in Brazil. Previous experience submitting clinical trials to ANVISA is required. Responsible for quality deliverables at the country level; follows project requirements and applicable...

**_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...