Pharmacovigilance Specialist
Aussicht: 160
Update Tag: 26-11-2025
Ort: Zaventem Flemish Brabant
Kategorie: Andere
Industrie:
Jobtyp: Full-time
Jobinhalt
Qplus consult offers high level- quality services for pharmaceutical companies. Within the pharmaceutical sector Qplus consult built a solid and strong reputation, therefore we are looking for a motivated, dynamic and flexible Pharmacovigilance Specialist.
What is the job about?
As part of the Case Management team, you will be working within our pharmacovigilance division located in Zaventem. You will be responsible for the case processing and an accurate documentation according to relevant procedures.
- You perform case receipt and processing
- You monitor all different sources for cases and perform worldwide literature screening
- You oversee case quality including analysis and reporting of trends in quality measures
- Responsible for the escalation of case-level quality issues
- Responsible for the quality control of you own work to guarantee the integrity and quality of records
- You are be the point of contact for case related activities with assigned pharmacovigilance partners
- You are the point of contact for audit-related activities related to cases
- You provide quality control of other case processors, you stand in for the second check
- You are responsible for the quality assurance of case management activities
- You perform case reviews
- You ensure compliance of reporting activities with timelines and criteria
What do we expect from you?
- You have a Bachelor or Master degree in Pharmacy or other university degree in Health Care
- You have at least 2 years of experience in Case Processing
- You have an excellent level of English and Dutch
- You have a strong knowledge and understanding of medical terminology and clinical development processes
- You have competences in safety systems and medical coding
- You are detail-oriented
- You can work in stressful situations where deadlines need to be respected
- You have the ability to take responsibility and accountability
- You can maintain a competence in drug safety systems and coding
What do we offer?
- Working at Qplus consult offers a lot of opportunities where every day will be different and challenging
- You will work in a dynamic and fast-growing company with customers worldwide
- We offer an healthy working environment: sit-stands desks, desk bikes..
- Attractive and competitive basic salary
- Secondary Advantages: insurances, meal vouchers, eco vouchers, company car + fuel card
- Possibilities of trainings in our training center and possibilities of evolution within the organisation
Who are we?
With our 6 service lines (Medical Affairs, Pharmacovigilance, Quality Management, Regulatory Affairs, Auditing and Training), we became an expert in our job within the pharmaceutical industry.
We attach a great importance to our values: client first, dedication, loyalty, passion, professionalism and performance.
Our main focus is to build a long-term relationship with each of our clients to provide a service of excellence in a timely and cost-efficient manner. To meet these expectations, we have a team of professional experts who are exceptionally highly trained and ready to provide excellent service every day.
You want to know more, take a look at our video: https://cutt.ly/6hU1k9B
Frist: 10-01-2026
Klicken Sie hier, um sich für einen kostenlosen Kandidaten zu bewerben
Job melden
ÄHNLICHE ARBEITEN
-
⏰ 02-01-2026🌏 Asse, Flemish Brabant
-
⏰ 27-12-2025🌏 Asse, Flemish Brabant
-
⏰ 02-01-2026🌏 Heverlee, Flemish Brabant
-
⏰ 25-12-2025🌏 Grimbergen, Flemish Brabant
-
⏰ 25-12-2025🌏 Asse, Flemish Brabant
-
⏰ 25-12-2025🌏 Zaventem, Flemish Brabant
-
⏰ 29-12-2025🌏 Leuven, Flemish Brabant
-
⏰ 22-12-2025🌏 Halle, Flemish Brabant
-
⏰ 06-01-2026🌏 Beersel, Flemish Brabant
-
⏰ 25-12-2025🌏 Zaventem, Flemish Brabant