Regulatory Affairs and Pharmacovigilance Manager
il y a 2 semaines
Our client, an established but also growing company in the pharmaceutical sector, is looking for a Regulatory Affairs and Pharmacovigilance Manager. This organization provides a unique opportunity to work with diverse products spanning medicines, medical devices, food supplements, and cosmetics, with focus on the pharmaceutical products, but this will give you more variety in the role. You can combine Regulatory and PV responsibilities, giving you a broader skill-set for your career.Benefits:Engage with a varied portfolio of products, offering dynamic work experiences and closer collaboration with the sales and marketing team. This gives you a better business perspective.Be part of a very friendly team with open communication, where you will feel more comfortable.Role Responsibilities:Ensure compliance with national and international regulations, contributing significantly to the organization's mission of prioritizing safety and quality.Coordinate with internal departments to support regulatory processes, enhancing cross-functional partnerships and professional growth.Approve regulatory validation of local artwork, product characteristics, patient information leaflets, and labelling.Actively participate in international regulatory discussions and forums, expanding your knowledge and exposure industry-wide.Act as Local Contact Person (LCP) for Pharmacovigilance BeLux.Requirements:Hold a Master's degree in Life Sciences.Possess several years of experience in regulatory affairs for the pharmaceutical industry.Experience with OTC or Consumer Health products is a big plus.Experience in Pharmacovigilance or as Local PV contact person is a big plus.Experience with registrations, variations and renewals in Belgium, BeLux or Benelux region.Fluent level in Dutch and English, French at least intermediate but ideally fluent.If this opportunity sounds like a fit, please apply here or send your CV to me, Annelies De Baere, on the NonStop Consulting website or on my Linkedin. On the other hand, if this job is not entirely for you feel free to share with any people from your network who would be interested.Do you have any disability or condition that could affect you in the application and interview process? Please share this information as part of your application, including any necessary adjustments you might need, so we can help make the process easier for you. We guarantee you this information will not have any negative effect on the interview process outcome.About NonStop: We are NonStop, a leading provider of staffing solutions throughout Europe and now also in the US. We're passionate about connecting talent with opportunity and work non-stop to support our clients in hiring the best talent for their teams. Feel free to pop over to our website, NonStop Consulting (https://www.nonstopconsulting.com), for more information, to browse all our roles, or to let us know how we can help you.
-
Regulatory Affairs and Pharmacovigilance Manager
il y a 2 semaines
East Flanders, Belgique NonStop Consulting Temps pleinOur client, an established but also growing company in the pharmaceutical sector, is looking for a Regulatory Affairs and Pharmacovigilance Manager. This organization provides a unique opportunity to work with diverse products spanning medicines, medical devices, food supplements, and cosmetics, with focus on the pharmaceutical products, but this will give...
-
Regulatory Affairs Manager
il y a 1 semaine
Flanders, Belgique CareForce One Temps pleinGreat new opportunity for a Regulatory Affairs Manager to join the Belgian affiliate of a mid-size pharmaceutical company that recently acquired new molecules, mainly Orphan Drugs / Oncology.JOB SCOPE:You will be the key partner to the local organization for all Regulatory (RA) and some Pharmacovigilance (PV) / Patient Safety matters. This is a great...
-
Senior Director, Regulatory Affairs
il y a 7 jours
East Flanders, Belgique WhatJobs Temps pleinSenior Director, Regulatory Affairs - CMC, Regulatory Operations & Lifecycle Management Join to apply for the Senior Director, Regulatory Affairs - CMC, Regulatory Operations & Lifecycle Management role at Perrigo Company plc Get AI-powered advice on this job and more exclusive features. At Perrigo, we are driven by our mission to Makes Lives Better Through...
-
Associate Director
il y a 2 semaines
East Flanders, Belgique WhatJobs Temps pleinAssociate Director - CMC Regulatory Affairs Join to apply for the Associate Director - CMC Regulatory Affairs role at Perrigo Company plc Description Overview As Associate Director, you will lead the development and execution of cutting-edge Chemistry, Manufacturing & Control (CMC) strategies, ensuring the highest standards of regulatory excellence across...
-
Medical Writer
il y a 15 heures
Flanders, Belgique Actalent Temps pleinIn this hands‐on role, you'll be at the heart of Post‐Market Clinical Follow‐Up (PMCF) and Post‐Market Surveillance (PMS) activities—driving best practices, ensuring compliance, and shaping smarter, safer medical technologies. You'll draft and maintain PMCF plans and evaluation reports, align findings across clinical evaluations, and contribute to...
-
Chief Technology Officer
il y a 3 semaines
East Flanders, Belgique WhatJobs Temps pleinThe Chief Technology Officer (CTO) leads the Development team and oversees all IT initiatives, ensuring the successful delivery of high-quality software solutions, IT systems, and processes. This role ensures technological excellence, operational stability, and the achievement of strategic development goals. KEY RESPONSIBILITIES Define and execute a clear...
-
Therapeutic Area Lead
il y a 1 semaine
Flanders, Belgique CareForce One Temps pleinWe have a very interesting opportunity for a Therapeutic Area Lead (MD) to join a biotech company with an impressive pipeline and eminent launches. You will play a key role in shaping the medical and scientific direction of the local organization and lead the team of Medical Affairs Professionals. An MD degree and experience in a Medical Affairs Department...
-
Early Development Global Study Data Leader
il y a 5 jours
East Flanders, Belgique WhatJobs Temps pleinEarly Development Global Study Data Leader Join to apply for the Early Development Global Study Data Leader role at Sanofi Location & Work Arrangement Location: Gent, Belgium Work arrangement: hybrid, minimum 3 days/week in the office About the Job Global Study Data Leader is responsible for leading the end-to-end data management activities and associated...
-
Portfolio Senior Manager
il y a 5 jours
Flanders, Belgique PeakSeek Temps pleinOur client, a leading infrastructure and renewables fund is looking for strong additions to their Asset Management / Portfolio teamResponsibilities Manage the full lifecycle performance of infrastructure and renewable energy assets, including monitoring KPIs, budgets, contracts, and risk exposure.Lead financial and operational reporting for investors,...
-
Production Supervisor
il y a 1 semaine
East Flanders, Belgique Hays Temps pleinAre you eager to contribute to the manufacturing of innovative treatments? Join a cutting-edge biotechnology company specializing in cell therapies. In a highly regulated GMP environment, you will supervise the production of advanced therapies. This role places you at the heart of manufacturing life-changing solutions for patients. MissionYou will be...