Regulatory Affairs Sr. Analyst

 Are you passionate about ensuring regulatory compliance for pharmaceutical products? Do you have experience in regulatory affairs and a strong understanding of the submission process? We are looking for a Regulatory Affairs Sr. Analyst to join our team at Novo Nordisk. If you are ready for a new challenge and want to make a difference in the pharmaceutical...

**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...

Regulatory Affairs Analyst (Clinical Trials) **Category**:Reg Affairs & Safety Pharmacovigilance**Location**:São Paulo, São Paulo, BR- **The Position**- Your responsabilities includes: - Develop Informed Consent Forms and regulatory dossiers for initial submissions, amendments, and notifications. - Manage the submission and approval process for trial...

SR IT BUSINESS ANALYST - REGULATORY (Nº DO VAGA: TEC000341) ** Descrição **The analyst will be responsible for**: - Support of transversal departments in the bank, but mainly focused on Client Management - Functional and technical specification - Solution design skills - Architecture diagrams ** Qualificações **Requirements**: - Higher Education -...

timely performance of work within a project scope to the quality expectations of PC and the client. When serving as a Project Lead or Work Stream Lead, a consultant secures the work of the entire team or work stream is delivered on time and that it meets client’s and PC’s quality. **Skills and knowledge**: Regulatory Affairs Consultant should have solid...

About AbbottAbbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will...

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you've got big plans '“ so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix...

Product Steward who have the overall coordination to manage product stewardship reviews (e.G GHS regulations), existing and emerging regulations, labelling and other requirements which comprehends Latin America region. These activities may include the development of safety data sheets and cross functional trainings;Ensure company operatesin conformity with...

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...

**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...

**What We Want** - ** Detail-oriented process improvers**. Critical thinkers who naturally see opportunities to develop and optimize work processes - finding ways to simplify, standardize and automate. - ** Self-directed imitators. **People who take ownership of their work and need no prompting to drive productivity, change, and outcomes. - ** Analytical...

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...

**JOB PURPOSE** Sr. Compliance Analyst role will involve a more comprehensive understanding and execution of complex compliance processes through several international laws and regulations and entities, and will be responsible for implementing and executing complex risk and compliance assessments, legal and regulatory analysis and updates, complex due...

Come to one of the biggest IT Services companies in the world!! Here you can transform your career!Why to join TCS? Here at TCS we believe that people make the difference, that's why we live a culture of unlimited learning full of opportunities for improvement and mutual development. The ideal scenario to expand ideas through the right tools, contributing to...

Come to one of the biggest IT Services companies in the world!! Here you can transform your career!Why to join TCS? Here at TCS we believe that people make the difference, that's why we live a culture of unlimited learning full of opportunities for improvement and mutual development. The ideal scenario to expand ideas through the right tools, contributing to...

Role: Regulatory Reporting Analyst. Position Type: Full-Time Contract (40hrs/week) Contract Duration: 6-12 months (with the ability to extend and a potential to convert to Full Time) Work Time zone: US PST Work Schedule: 8 hours/day (Mon-Fri) Location: 100% remote (resource can work from anywhere in Brazil or Mexico) ...

Ashland Inc. Are you the kind of person that is always thinking, sketching, seeking, and adjusting? Who needs to understand how things work and then figure out how they can work better? Are you a passionate, tenacious, solver who loves to work with others who share your drive? Are you positive, constructive, and ingenious? Are you always solving? Then...

Job Overview: Responsible for creation/revision and compilation of stability data and annual product quality review documents for submission by Fortrea clients to LATAM and oversight of the same. Should be proficient in English, Portuguese, Spanish languages. Knowledge of LATAM quality regulations. Summary of Responsibilities: These statements...

Job Overview: Responsible for creation/revision and compilation of stability data and annual product quality review documents for submission by Fortrea clients to LATAM and oversight of the same. Should be proficient in English, Portuguese, Spanish languages. Knowledge of LATAM quality regulations. Summary of Responsibilities: These statements are...

Come to one of the biggest IT Services companies in the world!! Here you can transform your career! Why to join TCS? Here at TCS we believe that people make the difference, that's why we live a culture of unlimited learning full of opportunities for improvement and mutual development. The ideal scenario to expand ideas through the right tools, contributing...