9 publicaciones de empleo destacadas de director of regulatory affairs en madrid, md (¡Están contratando!)

Senior Specialist Quality & Regulatory Affairs EMEA
Henry Schein Services GmbH —Madrid, Madrid provincia
- Jornada completa
- Inglés
- Project management
- Grado
Director International Commercialization Immunology
Regeneron —Madrid, Madrid provincia
- De 96.000 € a 160.000 € al año
- Máster
- Project management
- Grado
- Seguro dental
- Vacaciones pagadas
12d
Sr Director, Drug Development Lead
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Microsoft Powerpoint
- Microsoft Excel
- Doctorado
- Teletrabajo opcional
6d
Principal, Regulatory Science and Strategy - Real World Solutions
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Doctorado
- Inglés
- Máster
- Teletrabajo opcional
3d
Client Partner, Strategy Consulting Large Pharma Advisory, 1 year contract
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Trabajo híbrido
- Ventas
5d
Pricing & Market Access Lead, Iberia
Mundipharma —Madrid, Madrid provincia
- De 120.000 € a 125.000 € al año
- Jornada completa
- Español
- Marketing
- Hospital
Risk Manager
Sinclair —San Fernando de Henares, Madrid provincia
- Trabajo híbrido
- Inglés
- Máster
Sr Medical Project Manager
Gilead Sciences —Madrid, Madrid provincia
- Jornada completa
- Español
- Doctorado
- Inglés
EMEA Marketing Director
Insightec —Madrid, Madrid provincia
- Jornada completa
- Ventas
- Sistemas ERP
- Inglés
Solicitud rápida

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Senior Specialist Quality & Regulatory Affairs EMEA

Henry Schein Services GmbH -
Madrid, Madrid provincia

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Detalles del empleo

Jornada completa

Cualificaciones

Inglés
Project management
Grado

Descripción completa del empleo

Supports EMEA-wide QA/RA operations, participating to EMEA QA/RA Management meetings, documenting EMEA policies, accompanying the Snr. Director QA/RA EMEA to perform quality visits to countries and issue gap analysis, ensures CAPA follow-up on identified issues and support countries in implementing solutions within the Global Distribution Group Henry Schein Sites in EMEA.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Supports EMEA-wide QA/RA operations, documenting EMEA policies and provides support to implement the EMEA Quality Management System.
Supports to perform quality & regulatory visits and /or audits to countries and issues gap analysis, ensures CAPA follow-up and related documentation on identified issues and support countries in implementing solutions.
Organizing virtual, onsite, and offsite regional meetings, including logistics, agendas and close follow-up on decided actions with related functional / country QA/RA Lead.
Support and assistance to Exec. Director QA & RA EMEA and the EMEA QA/RA Team
Support to multiple projects, tracking timelines, and ensuring successful outcomes for EMEA-wide QA/RA initiatives.
Maintenance of eQMS and Quality Document Management Tool
Oversight of change control activities and CAPA follow-up, timely closure
Provides support to the country QA/RA Teams in Quality related topics to ensure compliance according GDP and MDR.
- Implementation of regulatory requirements and continuous improvement, support to ongoing transformation projects and product launch activities
- Support roll-out eQMS implementation in identified countries. o Inspection readiness initiatives and to roll- of required tools o Conduct and oversee quality training and compliance communications.
- Assits PRRC and EC Rep responsibilities such as adverse event reporting, post-market surveillance and FSN management
- Other tasks and projects as needed

Physical Activities:

Job holder based in any country in EMEA
Home based – ready to travel regularly (up to 30%)

QUALIFICATIONS:

Experience:

Quality Management, Project Management experiences, Medical Device
Experiences, Pharmaceutical (GDP) experience is a plus
MDR /IVDR Regulations/ ISO 13485
Validation of (computerized systems) and Risk management (FMEA) knowledge is a plus

Education:

Bachelor’s degree in Life Sciences, Pharmacist, Biomedical Engineering, Business management or a related field.

Specialise d Knowledge and Skills:

Knowledge and understanding of Quality Management Systems and Project Management
Quality System process implementation and maintenance to meet ISO 13485:2016; GDP and MDR.
Solution oriented, problem-solving attitude, pragmatic, high adaptability and flexibility
Ability to work in a matrix, regional environment with different departments and countries
English speaker
Good communication skills and stakeholder management

Other:

Balances a sense of urgency of time pressures with adherence to all regulatory requirements.
Sensitive in dealing with confidential Information
Demonstrates advanced oral and written communication skills
Must be fluent in written and spoken English

Information on pay transparency pursuant to Directive (EU) 2023/970

Please note that we comply with the relevant legal obligations regarding pay transparency, in particular those set forth in the EU Pay Transparency Directive (Directive (EU) 2023/970) and its respective national implementation.

In this context, we will inform you of the starting salary or the corresponding salary range for the advertised position no later than before the first job interview or before a personal discussion of your application. This information is based on objective, gender-neutral criteria established for the position in question.

Please note that we will not ask about your current or previous salary during the rest of the process in order to ensure equal pay.
This notice does not constitute a claim to the conclusion of an employment contract or to a specific salary.

Information on pay transparency in accordance with Directive (EU) 2023/970

Please note that we comply with the relevant legal obligations regarding pay transparency, in particular those set forth in the EU Pay Transparency Directive (Directive (EU) 2023/970) and its respective national implementation.
In this context, we will inform you of the starting salary or the corresponding salary range for the advertised position no later than before the first interview or before a personal discussion of your application. This information is based on objective, gender-neutral criteria established for the position in question.
Please note that, to ensure equal pay, we will not ask about your current or previous salary at any later stage of the process.
This notice does not constitute a guarantee of an employment contract or of a specific salary.

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director of regulatory affairs empleos en madrid, md

Senior Specialist Quality & Regulatory Affairs EMEA

Director International Commercialization Immunology

Sr Director, Drug Development Lead

Principal, Regulatory Science and Strategy - Real World Solutions

Client Partner, Strategy Consulting Large Pharma Advisory, 1 year contract

Pricing & Market Access Lead, Iberia

Risk Manager

Sr Medical Project Manager

EMEA Marketing Director

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