Qplus consult is op zoek naar een Administratief Bediende
Qplus consult biedt hoogwaardige diensten voor farmaceutische bedrijven. Binnen de farmaceutische sector heeft Qplus consult de voorbije jaren een solide en sterke reputatie opgebouwd. Met een gloednieuw kantoor gelegen in Zaventem, zijn ze op zoek naar een gemotiveerde, dynamische en flexibele Administratief Bediende.
De Job:
• Je biedt ondersteuning aan onze Case Management Associates
• Je bent verantwoordelijk voor het verzekeren van de kwaliteit en conformiteit van wetenschappelijke documenten en documenten omtrent geneesmiddelenbewaking
• Je biedt ondersteuning bij het opmaken en nakijken van medische documenten en documentatie omtrent geneesmiddelenbewaking
• Je zorgt dat de documentatie voldoet aan de vereiste wetgevingen en het bedrijfsbeleid van de klant
• Je volgt dossiers telefonisch en per mail op
Wat verwachten we van jou?
• Je hebt reeds 1 tot 3 jaar ervaring binnen een medisch secretariaat of bent bereid bij te leren in dit vakgebied
• Je spreekt en schrijft perfect Nederlands en Engels
• Je kan heel nauwkeurig te werk gaan
• Wetenschap boeit je mateloos
• Je bent flexibel ingesteld en bent stressbestendig
• Je bent leergierig en staat open om nieuwe kennis op te doen in een snel evoluerende werkomgeving
• Je wilt kwaliteit leveren en bent resultaatgericht
Wat bieden wij aan?
• Werken bij Qplus consult biedt veel kansen waarbij elke dag anders en uitdagend zal zijn
• Je komt terecht in een dynamisch en snelgroeiend bedrijf met klanten wereldwijd
• We bieden een gezonde werkomgeving aan: bureaufietsen, ergonomische stoelen, zit-sta bureaus, …
• Veel mogelijkheden tot extra opleidingen in ons eigen learning center
• Je start met een IBO contract en zal nadien een vast contract aangeboden krijgen
Wie zijn wij?
Met onze 6 servicelines (Medische zaken, geneesmiddelenbewaking, kwaliteitsmanagement, regelgevende zaken, audit en opleiding) werden we expert in onze job binnen de farmaceutische industrie.
Onze waarden staan voorop en we hechten hier dan ook veel belang aan: klant komt eerst, toewijding, loyaliteit, passie, professionaliteit en prestatie.
Onze belangrijkste focus is het opbouwen van langdurige relaties met elk van onze klanten om op een tijds- en kosten efficiënte manier een uitstekende service aan te bieden. Om aan deze verwachtingen te voldoen, hebben we een team van professionele experts die uitzonderlijk hoog opgeleid zijn en klaarstaan om elke dag een uitstekende service te verlenen.
Wil je meer weten over Qplus consult, bekijk dan zeker onze video.
Qplus consult is looking for a Case Management Associate
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 your own work to guarantee the integrity and quality of the records
• You are 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 Masters 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 + knowledge of Dutch is a surplus
• 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 a healthy working environment: sit-stand 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
Qplus consult is looking for a Drug Safety Advisor
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 Drug Safety Advisor.
What is the job about?
As a Drug Safety Advisor you will focus on providing high quality, comprehensive, technical and scientific information services for our customers on their product range, supporting and enhancing the safe and effective use of products, enabling our customers to make informed decisions about the product range.
• You provide a first line technical and scientific information service to internal PV-team and customers
• You handle all medical enquiries, in particular, adverse event reports and pregnancy reports, in line with procedures
• You take care of a medical evaluation of spontaneous adverse events
• You contribute to and perform medical assessments of the specific documents (e.g. safety profile of medicines, detected scientific literature, signals, cases etc.; Periodic and Development Safety reports, Risk Management Plans, DHPC etc.)
• You report cases to EMA within defined time frames and ensure appropriate levels of follow-up with reporters to fulfill all legal and regulatory requirements
• You ensure all appropriate reports are distributed to regulatory authorities, Ethics Committees and investigators within regulated timeframes
• You provide pharmacovigilance expertise to Risk Management planning cross-functional teams with input to formulation, implementation, maintenance and tracking of local RMPs
• You provide a comprehensive information service to external health care professionals and patients on the safety of company products in the scope of Risk Minimization Measures
• You undertake appropriate activities to train colleagues on obligations with regards to AE reporting
• You contribute to the PV audits and inspections as required
• As a part of the PV-team, you ensure any drug safety activities are in line and comply with EU-PV-legislation and procedures
What do we expect from you?
• You have a Master’s degree in science
• You have minimum 3 years of experience as Medical Advisor/ Drug Safety Advisor
• You have a fluent spoken + written level in English and Dutch, a fluent level of French is a surplus
• You have a strong knowledge of PV processes and European PV-legislation.
• You are able to work in a fast moving working environment
• Stress-resistant, working autonomously and flexible describe you
• Quality-oriented, therefore meticulous in figuring out and formatting your work
• Result-oriented
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 a healthy working environment: sit-stands desks, desk bikes, …
• Attractive and competitive basic salary
• Advantages: insurances, meal vouchers, eco vouchers, company car + fuel card
• Possibilities of trainings and evolution
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 our video.
Qplus consult is looking for a Junior Case Management Associate
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 Junior Case Management Associate.
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 the records
• You are 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 an excellent level of English + knowledge of Dutch is a surplus
• 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 a 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
