Regulatory Affairs Qro

**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...

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...

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...

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...

**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...

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,...

Posted 17-Apr-2024 Job type Full time Country Mexico Location Tultitlan, Mexico Lead recruiter Abril Lugo Function Legal Corporate Affairs Reporting Line Legal Director Latinoamerica & Caribbean On-site/Remote On-site Level of experience Professional (Management) Contract type Permanent YOUR OPPORTUNITY Your Opportunity This is a unique opportunity to be...

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,...

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,...

Site Name: Mexico City Torre Mitikah Posted Date: May 13 2024 Intern,Regulatory Affairs, 2024 Modelo híbrido: mínimo 2 días en el sitio por semana Ayúdanos a adelantarnos a la enfermedad junto con nuestra Área de Asuntos Regulatorios Formación requerida: Estudiante activo Químico farmacobiólogo, ingeniero farmacéutico, ingeniería...

Are You Ready to Make It Happen at Mondelēz International? Join our Mission to Lead the Future of Snacking. Make It With Pride. You execute the scientific and regulatory affairs strategy for your respective category or categories and geographical area using your scientific and regulatory expertise and are responsible for the regulatory and policy...

. **Qualifications** **Job**: Environmental Health & Safety - Supply Chain **Primary Location**: Latin America-MX-CMX - **Job Type**: Standard **Schedule**: Part-time **Shift**: 1st (Day) Shift **Job Number**: 2223555 We welcome people with all types of disabilities.

Regulatory & Scientific Affairs Jr Manager CMDXMain mission as a RSA Manager for Nestlé Mexico is to ensure functional leadership both internally and externally on specific regulatory topics through the development of Group's positions and policies. You will also represent Nestlé in influencing activities with national authorities under the scope of the...

Responsible for the management of the clinical development of Regenerative Medicine. The Medical Director will have a strong understanding of all phases of regenerative product development, including clinical trial management, medical monitoring, and will have extensive experience in collaboration with Clinical Operations, Research and Clinical...

JOB SUMMARY An Investigator Initiation Package (IIP) Sr Associate will ensure Pfizer maintains compliance with all requirements relating to release of investigational Product (IP) to clinical trial sites. Members of this team hold responsibility for verifying presence and consistency of required investigator related documents in the electronic Trial Master...

MEDICAL: - Provides support and the necessary medical and scientific information of Pfizer Biopharmaceutical Group products to internal and external customers assuring compliance with Corporate and Local Procedures and applicable regulations providing full support to our local medical objectives.- Collaborates with Drug Safety Unit, Global/Regional...

**Description** **Site Start-Up & Regulatory Specialist I** Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer...

Sobre nuestro cliente Empresa multinacional, con una rápida expansión gracias a su alta tecnología innovadora y de acceso para especialidades de alta complejidad Descripción Principales Responsabilidades: 1. Participar y abogar con grupos externos de la industria para implementar regulaciones que beneficien a la industria y la salud pública. ...