24 Empregos para Regulatory Affairs - Brasil

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As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow, Barrigel, Deknatel, QuikClot, LMA, Pilling, Rüsch, UroLift and Weck – trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.

Latin America - The Latin America Region of Teleflex is headquartered in Morrisville, North Carolina, and supports our customers, distributors, sales managers and specialists in Mexico, Brazil, Colombia, Chile, Argentina and Puerto Rico. The Latin America Region sells a broad spectrum of medical devices and related products in the fields of vascular and interventional access, surgical, anesthesia, cardiac care, urology, emergency medicine and respiratory care. As Teleflex grows and expands its portfolio, we will continue to grow our presence in Latin America. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.

This developing-level Regulatory Affairs position supports the Brazil Regulatory Affairs group to prepare
submission and registration documents supporting new or existing product offerings. The candidate must
work effectively with cross-functional groups and global regulatory affairs contacts to maintain Brazil
clearances/approvals.

• Understand regulatory processes, guidelines, and guidance documents and what they mean to the
organization.
• Communicate with internal stakeholders.
• Interface with various departments to collect and organize required documentation materials.
• Data entry, remediation, and maintenance of various regulatory databases.
• Assist in compiling new or revised medical device submissions and dossiers for import permits.
• Begin education on relevant domestic and Latin American regulatory requirements for medical
devices.
• Support the Regulatory Impact Assessment process.
• Discuss about GAP Assessments regarding regulatory updates.
• Provide administrative support to the Brazil Regulatory Affairs group, including securing certified
copies, processing payment requests, and coordinating dossier deliveries to third parties.
• Perform regulatory due diligence process
• Manage INMETRO certificates
• Lead local projects with orientation.
• Comply with Teleflex’s Code of Ethics, including all company policies, rules, procedures, and
housekeeping standards.

• Bachelor’s degree in a science or engineering field.
• 5 years’ experience with Class I or II medical devices
• Experience in INMETRO certification (preferable)
• Experience with Class III or IV medical devices (preferable)
• Languages – English required

• Strong communication skills (verbal and technical writing)
• Orientation to teamwork, problem-solving ability, customer focus, and a commitment to quality
• Strong organization skills, multi-tasking, meeting deadlines, and being detail-oriented.
• Knowledge of electronic document management systems

• Ability to apply Business and Regulatory Affairs ethical standards; analytical and critical thinking
skills.
• Hability to manage the tasks and meet the deadlines.
• Proficient in MS Word, Excel, PowerPoint, and Outlook.
• Preferred: understanding of domestic and international medical device regulations

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

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, process/document regulatory risk assessments, and provide support, expertise and represent the unit with other functional units, sponsors, researchers and/or regulatory authorities. Ensure high quality, timely service delivery processes are maintained in accordance with corporate, industry and regulatory standards and guidelines. May be required to coach peers and/or provide input for staff performance reviews.

• Coordinate the day to day delivery of regulatory services and processes, including compilation of regulatory filings/submissions/revisions for projects, third party vendors and clinical sites.
• Conduct or assist with regulatory and/or safety reviews, create regulatory-related tools, educational/training materials, and remain current on all aspects of clinical research regulatory requirements and industry best practices, communicating changes to project leaders in a timely manner.

• As the corporate subject specialist in regulatory affairs, provide regulatory, ethics and/or pharmacovigilance guidance and support to project stakeholders.
• Represent the unit at project meetings, assisting with project education/regulatory tool development, at regulatory reviews and audits, with clients ensuring expectations are managed and met, with regulatory, ethics and government representatives and, when appropriate, respond to regulatory queries on behalf of the client.

• Identify changes in clinical research regulatory requirements and industry best practices and recommend, implement, and maintain corporate regulatory strategies, working with other experts (safety, quality assurance) when appropriate, to meet or exceed compliance requirements of evolving regulatory initiatives.
• Participate in specialized conferences/meetings to increase knowledge as needed.

• Regularly respond to registration requests and work with project teams to identify regulatory requirements.
• Assist in the preparation of regulatory submissions and support summaries.
• Ensure project/clinical site files and documents are developed, maintained, revised, archived and/or destroyed in accordance with project and regulatory requirements and that all project stakeholders are fully informed and trained on all applicable regulatory requirements.

• Applicants should have a minimum of an undergraduate degree and 4-6 years of relevant experience in Clinical Research/Regulatory Affairs.
• The successful candidate will possess strong knowledge of LATAM clinical trial regulations.
• Fluency in English and Spanish (written and verbal) required.

• Home-based
• *Accommodations for job applicants with disabilities are available upon request.

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, process/document regulatory risk assessments, and provide support, expertise and represent the unit with other functional units, sponsors, researchers and/or regulatory authorities. Ensure high quality, timely service delivery processes are maintained in accordance with corporate, industry and regulatory standards and guidelines. May be required to coach peers and/or provide input for staff performance reviews.

• Coordinate the day to day delivery of regulatory services and processes, including compilation of regulatory filings/submissions/revisions for projects, third party vendors and clinical sites.
• Conduct or assist with regulatory and/or safety reviews, create regulatory-related tools, educational/training materials, and remain current on all aspects of clinical research regulatory requirements and industry best practices, communicating changes to project leaders in a timely manner.

• As the corporate subject specialist in regulatory affairs, provide regulatory, ethics and/or pharmacovigilance guidance and support to project stakeholders.
• Represent the unit at project meetings, assisting with project education/regulatory tool development, at regulatory reviews and audits, with clients ensuring expectations are managed and met, with regulatory, ethics and government representatives and, when appropriate, respond to regulatory queries on behalf of the client.

• Identify changes in clinical research regulatory requirements and industry best practices and recommend, implement, and maintain corporate regulatory strategies, working with other experts (safety, quality assurance) when appropriate, to meet or exceed compliance requirements of evolving regulatory initiatives.
• Participate in specialized conferences/meetings to increase knowledge as needed.

• Regularly respond to registration requests and work with project teams to identify regulatory requirements.
• Assist in the preparation of regulatory submissions and support summaries.
• Ensure project/clinical site files and documents are developed, maintained, revised, archived and/or destroyed in accordance with project and regulatory requirements and that all project stakeholders are fully informed and trained on all applicable regulatory requirements.

• Applicants should have a minimum of an undergraduate degree and 4-6 years of relevant experience in Clinical Research/Regulatory Affairs.
• The successful candidate will possess strong knowledge of LATAM clinical trial regulations.
• Fluency in English and Spanish (written and verbal) required.

• Home-based
• *Accommodations for job applicants with disabilities are available upon request.

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, process/document regulatory risk assessments, and provide support, expertise and represent the unit with other functional units, sponsors, researchers and/or regulatory authorities. Ensure high quality, timely service delivery processes are maintained in accordance with corporate, industry and regulatory standards and guidelines. May be required to coach peers and/or provide input for staff performance reviews.

• Coordinate the day to day delivery of regulatory services and processes, including compilation of regulatory filings/submissions/revisions for projects, third party vendors and clinical sites.
• Conduct or assist with regulatory and/or safety reviews, create regulatory-related tools, educational/training materials, and remain current on all aspects of clinical research regulatory requirements and industry best practices, communicating changes to project leaders in a timely manner.

• As the corporate subject specialist in regulatory affairs, provide regulatory, ethics and/or pharmacovigilance guidance and support to project stakeholders.
• Represent the unit at project meetings, assisting with project education/regulatory tool development, at regulatory reviews and audits, with clients ensuring expectations are managed and met, with regulatory, ethics and government representatives and, when appropriate, respond to regulatory queries on behalf of the client.

• Identify changes in clinical research regulatory requirements and industry best practices and recommend, implement, and maintain corporate regulatory strategies, working with other experts (safety, quality assurance) when appropriate, to meet or exceed compliance requirements of evolving regulatory initiatives.
• Participate in specialized conferences/meetings to increase knowledge as needed.

• Regularly respond to registration requests and work with project teams to identify regulatory requirements.
• Assist in the preparation of regulatory submissions and support summaries.
• Ensure project/clinical site files and documents are developed, maintained, revised, archived and/or destroyed in accordance with project and regulatory requirements and that all project stakeholders are fully informed and trained on all applicable regulatory requirements.

• Applicants should have a minimum of an undergraduate degree and 4-6 years of relevant experience in Clinical Research/Regulatory Affairs.
• The successful candidate will possess strong knowledge of LATAM clinical trial regulations.
• Fluency in English and Spanish (written and verbal) required.

• Home-based
• *Accommodations for job applicants with disabilities are available upon request.

Overview

Why should you join dLocal? dLocal enables the biggest companies in the world to collect payments in 40 countries in emerging markets. Global brands rely on us to increase conversion rates and simplify payment expansion effortlessly. As both a payments processor and a merchant of record where we operate, we make it possible for our merchants to make inroads into the world’s fastest-growing, emerging markets.

By joining us you will be a part of an amazing global team that makes it all happen, in a flexible, remote-first dynamic culture with travel, health and learning benefits, among others. Being a part of dLocal means working with 1000+ teammates from 30+ different nationalities and developing an international career that impacts millions of people’s daily lives. We are builders, we never run from a challenge, we are customer-centric, and if this sounds like you, we know you will thrive in our team.

What’s the opportunity?

We are looking for a Regulatory Compliance Officer to join our team in Brazil. In this role, you will be a key partner in ensuring that dLocal’s operations and legal entities remain fully compliant with all applicable regulations, while also enabling the company’s growth. You’ll serve as both a trusted advisor and a regulatory gatekeeper , helping protect the business from legal, regulatory, and reputational risks. You will work closely with cross-functional teams, regulators, and supervisory authorities, ensuring smooth communication, strong governance practices, and timely delivery of all compliance requirements.

• Ensure dLocal’s operations fully meet legal and regulatory requirements, maintaining a proactive compliance posture.
• Build and maintain strong, transparent relationships with supervisory authorities and regulators, ensuring accurate and timely communication.
• Support and coordinate responses for regulatory and statutory audits, from preparation through follow-up.
• Maintain the compliance calendar, ensuring all filings, reports, and regulatory returns are submitted accurately and on time.
• Partner with internal stakeholders to promote best practices, raise compliance awareness, and support sound decision-making at every level.
• Monitor new laws, regulations, and industry trends to advise the business and adapt processes proactively.

• Bachelor’s degree in Law or a related field (Master’s degree is a plus).
• Proven experience as a Regulatory Officer, Legal Advisor, or in a similar role, preferably in financial services, payments, e-commerce, or law.
• Strong knowledge of Brazilian regulations, especially Central Bank of Brazil (Bacen) requirements.
• Fluent English (written and spoken) — other languages are a plus in our global environment.
• Experience in an international company, financial institution, e-commerce platform, or law firm is a plus.
• Detail-oriented, proactive, and able to navigate complex environments with both analytical rigor and practical business sense.

Besides the tailored benefits we have for each country, dLocal will help you thrive and go that extra mile by offering you:

• Remote work: work from anywhere or one of our offices around the globe!
• Flexibility: we have flexible schedules and we are driven by performance.
• Fintech industry: work in a dynamic and ever-evolving environment, with plenty to build and boost your creativity.
• Referral bonus program: our internal talents are the best recruiters - refer someone ideal for a role and get rewarded.
• Learning & development: get access to a Premium Coursera subscription.
• Language classes: we provide free English, Spanish, or Portuguese classes.
• Social budget: you'll get a monthly budget to chill out with your team (in person or remotely) and deepen your connections!
• dLocal Houses: want to rent a house to spend one week anywhere in the world coworking with your team? We’ve got your back!
• *For people based in Montevideo (Uruguay) applying to non-IT roles, 55% monthly attendance to the office is required

Our Talent Acquisition team is invested in creating the best candidate experience possible, so don’t worry, you will definitely hear from us. We will review your CV and keep you posted by email at every step of the process!

Also, you can check out our webpage, LinkedIn, Instagram, and YouTube for more about dLocal!

Overview

Regulatory Affairs Specialist (LATAM) 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, process/document regulatory risk assessments, and provide support, expertise and represent the unit with other functional units, sponsors, researchers and/or regulatory authorities. Ensure high quality, timely service delivery processes are maintained in accordance with corporate, industry and regulatory standards and guidelines. May be required to coach peers and/or provide input for staff performance reviews.

• Coordinate the day to day delivery of regulatory services and processes, including compilation of regulatory filings/submissions/revisions for projects, third party vendors and clinical sites.
• Conduct or assist with regulatory and/or safety reviews, create regulatory-related tools, educational/training materials, and remain current on all aspects of clinical research regulatory requirements and industry best practices, communicating changes to project leaders in a timely manner.
• As the corporate subject specialist in regulatory affairs, provide regulatory, ethics and/or pharmacovigilance guidance and support to project stakeholders.
• Represent the unit at project meetings, assisting with project education/regulatory tool development, at regulatory reviews and audits, with clients ensuring expectations are managed and met, with regulatory, ethics and government representatives and, when appropriate, respond to regulatory queries on behalf of the client.
• Identify changes in clinical research regulatory requirements and industry best practices and recommend, implement, and maintain corporate regulatory strategies, working with other experts (safety, quality assurance) when appropriate, to meet or exceed compliance requirements of evolving regulatory initiatives.
• Participate in specialized conferences/meetings to increase knowledge as needed.
• Regularly respond to registration requests and work with project teams to identify regulatory requirements.
• Assist in the preparation of regulatory submissions and support summaries.
• Ensure project/clinical site files and documents are developed, maintained, revised, archived and/or destroyed in accordance with project and regulatory requirements and that all project stakeholders are fully informed and trained on all applicable regulatory requirements.

• Applicants should have a minimum of an undergraduate degree and 4-6 years of relevant experience in Clinical Research/Regulatory Affairs.
• The successful candidate will possess strong knowledge of LATAM clinical trial regulations.
• Fluency in English and Spanish (written and verbal) required.

• Home-based
• Accommodations for job applicants with disabilities are available upon request.

• Mid-Senior level

• Full-time

• Legal

• Pharmaceutical Manufacturing

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, process/document regulatory risk assessments, and provide support, expertise and represent the unit with other functional units, sponsors, researchers and/or regulatory authorities. Ensure high quality, timely service delivery processes are maintained in accordance with corporate, industry and regulatory standards and guidelines. May be required to coach peers and/or provide input for staff performance reviews.

• Coordinate the day to day delivery of regulatory services and processes, including compilation of regulatory filings/submissions/revisions for projects, third party vendors and clinical sites.
• Conduct or assist with regulatory and/or safety reviews, create regulatory-related tools, educational/training materials, and remain current on all aspects of clinical research regulatory requirements and industry best practices, communicating changes to project leaders in a timely manner.

• As the corporate subject specialist in regulatory affairs, provide regulatory, ethics and/or pharmacovigilance guidance and support to project stakeholders.
• Represent the unit at project meetings, assisting with project education/regulatory tool development, at regulatory reviews and audits, with clients ensuring expectations are managed and met, with regulatory, ethics and government representatives and, when appropriate, respond to regulatory queries on behalf of the client.

• Identify changes in clinical research regulatory requirements and industry best practices and recommend, implement, and maintain corporate regulatory strategies, working with other experts (safety, quality assurance) when appropriate, to meet or exceed compliance requirements of evolving regulatory initiatives.
• Participate in specialized conferences/meetings to increase knowledge as needed.

• Regularly respond to registration requests and work with project teams to identify regulatory requirements.
• Assist in the preparation of regulatory submissions and support summaries.
• Ensure project/clinical site files and documents are developed, maintained, revised, archived and/or destroyed in accordance with project and regulatory requirements and that all project stakeholders are fully informed and trained on all applicable regulatory requirements.

• Applicants should have a minimum of an undergraduate degree and 4-6 years of relevant experience in Clinical Research/Regulatory Affairs.
• The successful candidate will possess strong knowledge of LATAM clinical trial regulations.
• Fluency in English and Spanish (written and verbal) required.

• Home-based
• *Accommodations for job applicants with disabilities are available upon request.

Join to apply for the Governmental & Regulatory Affairs Specialist role at UBS

Join to apply for the Governmental & Regulatory Affairs Specialist role at UBS

Job Reference #
BR

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 position who strengthens our Regulatory Relations LatAm team. In this role, you will be working in a dynamic and agile team and have pronounced visibility direct relationship with the Brazilian Regulators.

In particular, you will:

• be part of a team responsible for effectively coordinating and managing the relationship between UBS and local regulators regarding all prudential supervisory interactions and responses to regulatory requests and inquiries
• globally communicate with the Regulatory Affairs teams in Switzerland and US as well as with the local UBS regulatory managers to ensure a consistent approach to regulatory issues
• proactively engage with, brief, and advise senior management on regulatory interactions within your coverage, and help to formulate an appropriate approach for regulatory communication
• provide guidance and advice to business and control & support functions to react to and deliver against regulatory requests and exercises
• monitor the execution and implementation of remedial supervisory actions and provide strategic guidance in relation to preparation for supervisory reviews
• track the new regulations applicable to the business coordinating the implementation within the Compliance and Business teams
  
  

• +6 years of work experience in a similar area (e.g.: legal, regulatory compliance or risk)
• a sound understanding of the financial sector regulatory landscape and developments and related concepts
• familiarity with Wealth Management and Investment Bank products and services- related matters
• an ability to work with experts across locations / functions; in particular with experts in regulatory, legal, compliance, and governance fields as well as with business representatives
• PowerPoint and Excel skills
• excellent proficiency in spoken and written English and Portuguese
• availability to work onsite in Sao Paulo's office
• ability with Data Management and Artificial Intelligence will be considered as a plus
  
  

• Seniority level Not Applicable

• Employment type Full-time

• Job function Legal, Finance, and Accounting/Auditing
• Industries Banking, Financial Services, and Investment Banking

Referrals increase your chances of interviewing at UBS by 2x

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EBANX is the leading payment platform connecting global companies with customers from the fastest-growing digital markets in the world.

Since the beginning of our journey, we have had one mission: to provide global access for everyone. We believe that transforming challenges into opportunities and making the impossible part of the journey is crucial! That's precisely why we created a payment technology that builds bridges between people and businesses every day in 29 rising markets across the globe.

We call ourselves ebankers, we are global thinkers, we value diversity, we foster creativity and we work hard to connect businesses and people worldwide through payments. Let's make history together?

As a Regulatory Affairs SR Analyst, your mission will be to strategically oversee and manage all aspects of regulatory compliance within the organization, ensuring adherence to relevant laws, regulations, and industry standards. You will support the development and implementation of robust regulatory strategies, provide expert guidance on complex regulatory matters, and proactively identify and mitigate regulatory risks.

You will also be responsible for:

• Assist in interpreting regulations for the company's business, especially in Payment Methods;
• Respond to regulatory notices and inspections;
• Assess the regulatory compliance of new products, services and features of the company's payment arrangements;
• Provide support for business decisions from a regulatory compliance perspective;
• Disseminate high ethical standards throughout the organization;
• Identify deficiencies (non-conformities) and monitor corrections;
• Give training about regulations for technical teams;

Main requirements for this position:

• Graduation in Law, Administration or related areas;
• Relevant experience in Regulatory Compliance activities;
• Advanced English;

What would be a plus?

• Experience with Payment Institution or Exchange will be considered a differential.

EBANX offers:

• Spanish, English, and Portuguese classes;
• Meal Allowance;
• Transportation voucher (if needed);
• WAVES - Program of goals and results (variable compensation);
• EBANX Play - Wellness (Gympass, e-Sports, SESC );
• EBANX Education: financial support for undergraduate, graduate, and MBA programs so you can develop important skills for your career;
• EBANX Skills: budget for workshops and courses;
• EBANX Flexible: Birthday Day Off;
• Semi-flexible hours (8 hours a day - Monday to Friday);
• EBANX Family: Daycare assistance, extended leave for caregivers and support program for children and pregnant women;
• EBANX Health: Health and Dental Insurance, with subsidy for dependents and medicine subsidy for ebankers;
• Life Insurance: Life Insurance 100% paid by EBANX;
• Blue Club: Exclusive discount for ebankers in bakeries, restaurants, courses, electronics stores, and more!

Follow us on LinkedIn and check out our Instagram to learn more about the #ebanxlife.