20 publicaciones de empleo destacadas en regulatory affairs (¡Están contratando!)

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Regulatory Affairs Officer, IQVIA Biotech
IQVIA —Ciudad de México, CDMX
- Administración de personal
- Microsoft Office
- Maestría
Professional Veterinary Affairs Digital Specialist
Hill's Pet Nutrition —Ciudad de México, CDMX
- Administración de personal
- Mercadotecnia
- Gestión de redes sociales
Regulatory Affairs Coordinator
MMATISS —Jardines del Pedregal, CDMX
Regulatory Affairs Specialist I
Merit Medical —Tijuana, B.C.
- Tiempo completo
- Word processing
- Inglés
- Licenciatura
20h
EV Charging & Energy Public Policy Manager, LATAM
Tesla —Colonia Lomas de Chapultepec, CDMX
- Inglés
- Disponible para viajar
- Negociación
Marketing & Regulatory Coordinator
Olmix —San José el Alto, Qro.
- Mercadotecnia
- Inglés
- Licenciatura
Postulación rápida
LATAM Government Affairs Director
Solventum —Ciudad de México, CDMX
- Tiempo completo
- Disponibilidad para viajar hasta un 50 %
- Experiencia en ventas
- Inglés
Life Sciences R&D Consultant/Manager
Accenture —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Disponible para viajar
Regulatory Postmarket Specialist
Intuitive Surgical —Mexicali, B.C.
- Doctorado
- Análisis de datos
- Inglés
9d
Customer Success Representative
ORBIS Compliance LLC —Ciudad de México, CDMX
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Postulación rápida
14d
Especialista de Asuntos Regulatorios Mexico & CAM
Phibro Animal Health Corporation —Guadalajara, Jal.
- Tiempo completo
- Inglés
- Microsoft Office
- Habilidades de organización
AML Advisor, U.S. National
SGI Global, LLC —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Microsoft Office
- Licenciatura
Postulación rápida
8d
GERENTE DE ASUNTOS REGULATORIOS
Amedirh TALENTO —Cuauhtémoc, CDMX
- Tiempo completo
- Trabajo híbrido
- Inglés
- Maestría
- Licenciatura
Postulación rápida
Flavorist |F&B | MX
Symrise —Cuautitlán, Méx.
- Tiempo completo
- Inglés
- Licenciatura
Postulación rápida
11d
Quality Management Systems (QMS) Coordinator
Foxconn Baja California, S.A. de C.V. —Tijuana, B.C.
- Tiempo completo
- Inglés
- Licenciatura
- Presencial
8d
Associate Director, Pharmacovigilance Country Head – Mexico
Moderna, Inc. —Ciudad de México, CDMX
- Tiempo completo
- Español
- Administración de personal
- Inglés
- Vacaciones adicionales o permisos con goce de sueldo
Local Study Associate Director - FSP
Parexel —Desde casa
- Home Office (Desde casa)
- Administración de personal
- Inglés
- Licenciatura
Regulatory Associate - AdPromo
サイネオス・ヘルス —Tlalnepantla, Méx.
- Contratos
11d
Compliance Engineer
Sensata Technologies, Inc. —Aguascalientes, Ags.
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
7d
Congress and Digital Channel Partner
Novartis —Insurgentes, QRoo.
- Tiempo completo
- Administración de personal
- Inglés
- Licenciatura

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Regulatory Affairs Officer, IQVIA Biotech

IQVIA -
Ciudad de México, CDMX

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Información del empleo

Cualificaciones

Administración de personal
Microsoft Office
Maestría
Licenciatura

Descripción completa del empleo

Key Responsibilities

Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing.

Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level .

Engage directly with clients to clarify clinical trial regulatory pathways, share lessons learned, and address feedback.

Engage with Competent Authorities in countries across multiple regions, as part of the clinical trial regulatory strategy for complex global studies

Monitor scope, deliverables, timelines, and budget; proactively mitigate risks and escalate issues as needed.

Provide guidance and feedback to junior colleagues; support training and continuous improvement initiatives.

Contribute to internal SOP reviews and present regulatory processes at full-service bid defenses.

Perform additional tasks assigned by Regulatory management to meet program goals.

Qualifications

Bachelor’s or Master’s degree in Life Sciences or related discipline.

3–4 years of relevant clinical trial regulatory experience within CRO or biotech/pharma.

Strong understanding of the R&D continuum (CMC, preclinical, clinical) and applicable laws, guidelines, and agency expectations for clinical trials.

Demonstrated expertise in at least one clinical trial regulatory domain (e.g., CMC, labeling).

Experience with clinical trial regulatory submission platforms and pathways, including but not limited to, EU CTR, Health Canada, US FDA IND submissions and/or systems in other regions such as LATAM or APAC. Biotech therapy area exposure welcomed.

Proficiency with Microsoft Office and regulatory publishing tools (e.g., eCTD systems); meticulous document management skills.

Excellent written and verbal communication, organization, and stakeholder-management abilities.

Proven ability to manage multiple projects; work in a fast-paced environment with competing priorities; and view obstacles as challenges to be handled with ease and grace; follow SOPs consistently, and exercise sound judgment on discrete tasks.

Problem-solving mindset with adaptability in fast-changing environments; self-motivated and collaborative.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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regulatory affairs empleos

Regulatory Affairs Officer, IQVIA Biotech

Professional Veterinary Affairs Digital Specialist

Regulatory Affairs Coordinator

Regulatory Affairs Specialist I

EV Charging & Energy Public Policy Manager, LATAM

Marketing & Regulatory Coordinator

LATAM Government Affairs Director

Life Sciences R&D Consultant/Manager

Regulatory Postmarket Specialist

Customer Success Representative

Especialista de Asuntos Regulatorios Mexico & CAM

AML Advisor, U.S. National

GERENTE DE ASUNTOS REGULATORIOS

Flavorist |F&B | MX

Quality Management Systems (QMS) Coordinator

Associate Director, Pharmacovigilance Country Head – Mexico

Local Study Associate Director - FSP

Regulatory Associate - AdPromo

Compliance Engineer

Congress and Digital Channel Partner

Quiero recibir la alerta de empleo más reciente para regulatory affairs

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