20 beste vacatures voor de functie van regulatory affairs in brussels, bru (nieuwe medewerkers gezocht)

Medical Advisor
Qplus consult —Melsbroek
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Medical Advisor

Qplus consult
Melsbroek

Nu solliciteren

Vacaturegegevens

Extralegale voordelen

Ecocheques
Elektronische maaltijdcheques

Kwalificaties

Geneeskunde
Doctoraat
Master

Volledige vacaturetekst

This job is located in Melsbroek (Kalkoven 5, 1820 Steenokkerzeel, Belgium) – please apply only if you live in Belgium and have a valid working permit for Belgium

What is the job about?

As a Medical Advisor with a Medical Doctor education degree, you focus on providing high-quality, comprehensive, and scientific information services to our customers regarding their product range. This involves supporting and enhancing the safe and effective use of products, enabling our customers to make informed decisions about their product range.

You provide a first-line scientific and medical information service to the internal pharmacovigilance (PV) team and customers.
You handle Medical Review/Assessment of all medical inquiries, Adverse Event Reports, and pregnancy reports, in line with procedures.
You take care of a medical evaluation of adverse reactions.
You contribute to and perform medical assessments of specific documents (e.g., safety profiles of medicines, detected scientific literature, signals, cases, etc.; Periodic and Development Safety reports, Risk Management Plans, DHPC, etc.).
You provide pharmacovigilance expertise to Risk Management planning cross-functional teams with input to the formulation, implementation, maintenance, and tracking of local RMPs.
You provide a comprehensive information service to external healthcare professionals and patients on the safety of company products within the scope of Risk Minimization Measures.
You contribute to PV audits and inspections as required.
As part of the PV team, you ensure any drug safety activities are in line with and comply with EU-PV-legislation and procedures.

What do we expect from you?

You have a Master’s degree in Medical Science as a Medical Physician.
You have 1-3 years of experience as a Medical Advisor/Drug Safety Advisor.
You work 5 days per week at our offices (on-site).
You have a strong knowledge of PV processes and European PV-legislation.
You have a minimum level of C1 or C2 in English; knowledge of another EU language is a plus.
You can work in a fast-paced working environment.
You are stress-resistant and work autonomously.
You are quality-oriented and meticulous in figuring out and formatting your work.
You are result-oriented.

What do we offer?

Working at Qplus Consult brings new challenges and opportunities every day.
You will be part of a dynamic, fast-growing company with a global customer base.
Our workplace fosters a healthy environment with fresh fruit, sit-stand desks, or desk bikes/treadmills.
Attractive and competitive basic salary.
Additional benefits like health insurance, meal vouchers, eco vouchers, and a mobility package.
Extensive training and great career growth opportunities.

Who are we?

With our 6 service lines (Medical Affairs, Pharmacovigilance, Quality Management, Regulatory Affairs, Auditing, and Training), we are experts in our field within the pharmaceutical industry. We emphasize our values: client first, dedication, loyalty, passion, professionalism, and performance.

Our main focus is to build long-term relationships with each of our clients to provide excellent service 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.

Ready to make an impact in the pharmaceutical sector?

Apply now by sending your resume and motivation letter to [email protected]!

Interesse?
Stuur uw CV en motivatie naar [email protected] met de vermelding ‘Medical Advisor’.

Bijkomende informatie kan eveneens op dit e-mailadres verkregen worden.

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Verfijn je zoekopdracht

regulatory affairs vacatures in brussels, bru

Medical Advisor

External Manufacturing Process Operations Excellence Lead

Stage affaires réglementaires

Senior Consultant/Account Director Technology (EU Policy)

Device Quality Engineer

Regulations Manager

R&D and PV Q Cross-Reg Integration Lead

Business Development Manager Africa

Data Science - Stage / Mémoire de master (F/H/X) - Durée minimum de 3 mois

Principal Statistical Methodologist (Belgium)

Impact Quality Lead GVP

Senior Account Manager Cell Therapy Technologies (UK&I, Benelux, France & Sweden)

Legal Counsel

Devices Industrialization Lead

Senior QA MES Consultant

Data Manager

External Manufacturing - Alliance Manager

Principal Statistical Methodologist

Project Engineer

Digital Laboratory Solutions Manager

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs in brussels, bru

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