20 meilleures offres (european affairs) (à pourvoir)

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Junior Consultant - Pharma
IQVIA —Kampenhout
- Temps plein
- Master
- Compétences en communication
RRA - Regulatory Affairs Project Manager with Toxicology experience - Plant Protection Products
Redebel —Saint-Amand
- Gestion de projet
IT Internship
EMVO (European Medicines Verification Organisation) —Bruxelles
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- Microsoft Office
- Java
Research Executive
Rud Pedersen Public Affairs Company AB —Bruxelles
- Stage
RRA - Regulatory Affairs Project Manager - Plant Protection Products
Redebel —Saint-Amand
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Food Regulatory & Specification Manager
What's Cooking? —Sint-Denijs-Westrem
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- Master
- Production
Managing Director and Head of Brussels Office
Investment Company Institute —Bruxelles
- De 200 000 € à 250 000 € par an
- Anglais
- Leadership
Postuler rapidement
Country Regulatory Assistant- PPP Department
Redebel —Saint-Amand
- Anglais
- Recherche
- Microsoft Office
Director, Corporate Reputation
FTI Consulting —Bruxelles-Capitale
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- Microsoft Excel
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- Bachelier
Customs Analyst
Nike —Laakdal
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- Agile
il y a 5 jours
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Mercury Engineering —Mons
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Regulatory Affairs Manager
Nipro —Malines
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Regulatory Counsel, Privacy Advisory and Engagement
Google —Bruxelles
- De 200 000 € à 205 000 € par an
il y a 5 jours
Research Executive - Energy & Industrials
Rud Pedersen Public Affairs Company AB —Bruxelles
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Quality Specialist (Distribution Center)
Abbott Laboratories —Machelen
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Associate Partner - Governance
AION Consulting —Bruxelles
- Master
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Drug Safety Advisor
Qplus consult —Melsbroek
- Doctorat
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CRM Functional Analyst Dynamics 365 & Power Platform
Orange Business —Evere
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Communication Officers - German
Esn —Bruxelles
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CRM Functional Analyst Dynamics 365 & Power Platform
MasORange —Evere
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Junior Consultant - Pharma

IQVIA -
Kampenhout

Soumettre votre candidature

Détails de l'emploi

Temps plein

Qualifications

Français
Master
Compétences en communication

Description complète du poste

Kampenhout, Belgium | Full time | Hybrid | R1549980

We are looking for a Junior Consultant to join our team.

Main Areas of Responsibility
As a junior consultant at IN2Pharma, you will be trained to support more senior colleagues in ensuring the client’s products meet the required standards of quality and safety and in ensuring regulatory compliance for a defined range of products of the client’s portfolio. This gives you the opportunity to acquire experience within one or several of the following domains:
Medical & Regulatory Affairs

Medical writing: expert reports, clinical evaluations, literature study
Medical education of sales representatives: product training on medicinal or healthcare products
Review and approve promotional material for medicinal and healthcare products
Adapt SPC, PIL and packaging materials in line with the registration file and legislation

Pharmacovigilance (PV)

Local Literature Review for adverse events on the MAH’s medicinal products
Assist in the PV quality system set-up or maintenance: PV SOPs, gap analysis, compliance check with applicable regulations
Training of MAH’s employees in PV awareness

Quality Assurance (QA)

Support the QP/RP in all aspects related to quality and compliance ensuring local requirements are met
Support the QP/RP in the administrative release to the market in compliance with procedures. This includes: QA check, CoA request, Artwork request, Contact with warehouse/supply,…
Investigate customer complaints and non-conformance issues

Technical Skill Requirements

Master degree in life sciences
Good knowledge of national and European regulations and legislations for medicinal products
Good communication skills in Dutch, French and English (both verbal and written)
Strong initiative, problem solver and good organizational skills
Accurate & efficient: concern for quality, compliance and consistency
Good communicator & team player

Our offer

A permanent full-time position with a competitive package and supplementary benefits
Challenging and alternating job as consultant within a dynamic team
Development opportunities by working on various projects for different pharmaceutical companies

IN2Pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects for pharmaceutical and healthcare industry in Benelux. Our offices are located in Kampenhout at the business center “Hof ter Loonst” and in Gentbrugge.

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.

Where you'll work

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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european affairs emplois

Junior Consultant - Pharma

RRA - Regulatory Affairs Project Manager with Toxicology experience - Plant Protection Products

IT Internship

Research Executive

RRA - Regulatory Affairs Project Manager - Plant Protection Products

Food Regulatory & Specification Manager

Managing Director and Head of Brussels Office

Country Regulatory Assistant- PPP Department

Director, Corporate Reputation

Customs Analyst

Logistics Manager

Regulatory Affairs Manager

Regulatory Counsel, Privacy Advisory and Engagement

Research Executive - Energy & Industrials

Quality Specialist (Distribution Center)

Associate Partner - Governance

Drug Safety Advisor

CRM Functional Analyst Dynamics 365 & Power Platform

Communication Officers - German

CRM Functional Analyst Dynamics 365 & Power Platform

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : european affairs

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Where you'll work

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