Regulatory Affairs Specialist

**Regulatory Affairs Specialist** **Major Tasks** - Provides operational support to Regulatory Affairs Management in active projects such as local regulatory strategy for New Drug Applications, local preparation for the New Molecules Committee and other projects. - Propose the local regulatory strategy for maintenance projects of the active registrations by...

In the context of a new project, we are looking for a Regulatory Affairs Specialist to join our teams in Mexico/LATAM. Responsibilities Provide guidance and support about Mexican and Central America legislation Contribute to the regulatory activities performed. Regulatory activities include pre licensing activities, new registration (sites and medicinal...

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...

Regulatory Affairs Analyst (Fixed Term) page is loaded Regulatory Affairs Analyst (Fixed Term) Postuler locations Mexico City, Mexico time type Temps plein posted on Offre publiée hier job requisition id R5646189 Viatris Healthcare México S. de R.L. de C.V Chez Viatris, nous envisageons la santé non pas telle qu'elle est mais telle qu'elle devrait...

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a...

Responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level for Europe, the United States, and other countries. Primary responsibilities are to ensure regulatory compliance for assigned product lines Other responsibilities include coordinating recalls, identifying relevant standards and guidance documents...

The legal team protects Red Bull, its people, partners and vendors by adding value to each product line and initiative. Legal is divided into Legal Business Partners for the Beverage Business and Corporate Projects, Specialist Departments and Centers of Expertise. The Regulatory Specialist assists the LATAM Regional team by offering technical and legal...

In the context of additional activities for one of our main clients, we are looking for a Regulatory Affairs Officer working from Mexico or Canada to manage post-MAA activities (Life Cycle Management) for the Canadian market. Responsibilities Management of post approval activities (Life Cycle Management) for the Canadian market Initiate change...

**JOB DESCRIPTION** **PURPOSE** Perform tasks at country level associated with Regulatory, Start-up (RSU) and Maintenance activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May participate in feasibility and/or site identification...

Job TitleRegulatory Affairs Supervisor Latam (Medical Equipment)Job DescriptionJob title:Regulatory Affairs Supervisor Latam (Medical Equipment)Your role:To formulate and implement the HPM Businesses and / or Markets long-range regulatory strategies for LATAM (Latin America).Main point of contact between BU, Market and Local Business Team for product...

**Requisition Number**7930** **Employment Type**:Regular** **Who we are** We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and...

Job Responsibilities: As a LATAM Government Affairs Manager, you have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: Establishing, maintaining, and executing a government affairs agenda to include maintenance of a bipartisan contact network...

Start-up & Regulatory Specialist page is loaded Start-up & Regulatory Specialist Apply locations Mexico City Mexico time type Full time posted on Posted 30+ Days Ago job requisition id 2412781 As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides...

ROLE DESCRIPTION - Support and facilitate interlocution with Government stakeholders to support Pfizer’s business in Mexico. - Contrinbute to the development and implementation of innovative strategic policy and public affairs platforms to advance Pfizer Mexico’s business and policy objectives, including but not limited to engaging government,...

**About Kerry**: - Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions - Under general supervision, serve...

**Description** **Job Description**: JOB TITLE: Site Start-Up & Regulatory Specialist II SELECT ONE: Clinical Solutions JOB CODE: 01022 REPORTS TO: Manager, Site Start-Up & Regulatory; or designee JOB SUMMARY Performs assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials. Responsible for...

Nome della sede: Mexico City Torre MitikahData di apertura: May Intern,Regulatory Affairs, 2024Modelo híbrido: mínimo 2 días en el sitio por semanaAyúdanos a adelantarnos a la enfermedad junto con nuestra Área de Asuntos Regulatorios Formación requerida: Estudiante activo Químico farmacobiólogo, ingeniero farmacéutico, ingeniería química,...

Nome della sede: Mexico City Torre MitikahData di apertura: May 13 2024Intern,Regulatory Affairs, 2024Modelo híbrido: mínimo 2 días en el sitio por semanaAyúdanos a adelantarnos a la enfermedad junto con nuestra  Área de Asuntos Regulatorios Formación requerida: Estudiante activo Químico farmacobiólogo, ingeniero farmacéutico, ingeniería química,...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions • Under general supervision,...