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                      marketing, communications, events, PR, marketing manager jobs in the R&D & Science category

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                      Arcq - Herent(3 days ago)
                      Job content The Quality Analyst will be responsible for facilitating management of Quality Events and Quality Risks through application of the company's Quality Event Management program, and the analysis of quality data including but not limited to internal/external audit, regulatory inspections, and QEM program. Translating data into knowledge and making best use of knowledge are essential to ach...
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                      VALESTA - Multiple locations(4 days ago)
                      Since we are frequently looking for experienced Medical science liaisons (MSL) to reinforce our team, don't hesitate to apply if you recognize yourself in following criteria: Do you have previous experience as MSL, or another experience within the pharmaceutical industry, f.e. as a medical writer, within medical information, as CRA, as medical representative.? Do you have a strong scientific backg...
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                      Arcq - Herent(9 days ago)
                      Job content The Quality Analyst will be responsible for facilitating management of Quality Events and Quality Risks through application of the company's Quality Event Management program, and the analysis of quality data including but not limited to internal/external audit, regulatory inspections, and QEM program. Translating data into knowledge and making best use of knowledge are essential to ach...
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                      Fast Track Diagnostics Luxembourg S.à r. l. - L-4354, Esch-sur-Alzette(11 days ago)
                      Fast Track Diagnostics, a Siemens Healthineers company, develops and commercializes worldwide multiplex real-time PCR (RT-PCR) assays to detect a wide range of viruses, bacteria, fungi and parasites. We are ISO 13485 certified since 2011. Our kits are used in all size labs, in the public and private sector. In the last years, FTD created a global distributor network that serves many countries worl...
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                      Progressive Recruitment - Mechelen(12 days ago)
                      ik ben momenteel naar iemand op zoek die tijdelijk op project basis, enkele verpakkingsontwikkelings project opzich neemt. PET flessen in verschillende formaten. De projecten zijn zowel voor ontwikkeling in fles als dop , dit is vooral optimalisatie projecten op basis van bestaande flessen en doppen. Profiel basis : ervaring met verpakkingen en project management/ coördinatie skills Doel is om pro...
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                      Pauwels Consulting NV - Job location not provided(1 day ago)
                      Job description Updates knowledge on related regulatory requirements, ensures adherence and compliance with local regulations and internal procedures Executes all start-up activities prior to site activation on assigned studies Prepares country level Informed Consent Form (ICF) and obtains ethics committees' and local regulatory authorities' approval Maintains and analyzes study start-up data (met...
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                      GlaxoSmithKline - 1330, Rixensart(1 day ago)
                      GSK is looking for a Scientist (M/F) Requisition ID: WD201814 Your Responsibilities: The incumbent will be responsible of the design of filling and devices process evaluation/ experimental protocols in collaboration with Drug Product (DP) Belgium (BE) project referent, for the experimental realizations and the redaction of the related reports. The person will collaborate with Early & Late projects...
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                      Pauwels Consulting NV - 1435, Mont-Saint-Guibert(1 day ago)
                      Job description Oversee the design and management of pre-clinical studies (GLP and non-GLP) for inclusion in regulatory documents, including PoC, pharmacology, toxicology, and biodistribution studies Manage contract research organizations (CROs) and external collaborations to support pre-clinical development programs Work closely with other functional areas and colleagues to ensure that all pre-cl...
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                      Pauwels Consulting NV - 1070, Anderlecht(1 day ago)
                      Company description Pauwels Consulting is a Belgian consulting firm with more than 520 experts in engineering, life sciences and IT. We offer consulting, project management and recruitment services to leading companies in Belgium and beyond. We have offices in Belgium, France, Germany and Switzerland (https://www.pauwelsconsulting.com/about/contact/) . Job description Analyzes and interprets data ...
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                      Pauwels Consulting NV - 4000, Liège(2 days ago)
                      Company description Pauwels Consulting is a Belgian consulting firm with more than 520 experts in engineering, life sciences and IT. We offer consulting, project management and recruitment services to leading companies in Belgium and beyond. We have offices in Belgium, France, Germany and Switzerland (https://www.pauwelsconsulting.com/about/contact/) . Job description Administers, maintains and co...
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                      Arcq - Herent(3 days ago)
                      You manage clinical trials from start to finish: you carry out pre-study visits, you initiate the trial, you are responsible for routine monitoring and closing visits about the quality standards and timelines You obtain and update essential documentation in compliance with ICH-GCP, Procedural Documents and local regulations both in a Trial Master File (eTMF) and Investigator Study File (ISF) You a...
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                      Hays Wavre - Flemish Brabant(3 days ago)
                      * Quality Event and Risk Management * GCP/GLP/GMP * Belgium, Flemish Brabant area Hays Life Sciences is looking for a Clinical Quality Systems Analyst - GCP (Good Clinical Practice) & GLP (Good Laboratory Practice) to join the Quality Assurance team in a global clinical contract research organization. As a Quality Systems Analyst, you will be responsible for facilitating management of Quality Even...
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                      Michael Page Belgium - 1000, Brussels(5 days ago)
                      Regulatory Affairs Specialist - OTC Products Global FMCG & OTC company Client Details Our client is one of the main actor within the FMCG & OTC world. In order to sustain their growth, they are today looking for a new regulatory affairs specialist in order to take care of the Regulatory Authorities on the Belgian Markets for their range of products. Description The successful candidate will have t...
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                      Keysight Technologies - 9051, Afsné(5 days ago)
                      Keysight Technologies is #1 in Electronic Design & Measurement products with over 12,500 employees across the globe, transforming today's measurement experience through innovations in wireless, modular, and software solutions. Through our 75-year history we have innovated through new business expansion. A strong product development business process created leadership in most product categories. Wh...
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                      Hays Wavre - Bruxelles(8 days ago)
                      Hays Life Sciences is recruiting a Real World Evidence (RWE) Data Scientist to join a Global Biopharmaceutical Company. The position is based preferably in Belgium, in the Brussels area, but other locations may be considered. * Epidemiology * Pharmacovigilance * Outcome research * Skilled in written and oral scientific presentations The RWE Data Scientist is a Lead Scientist position that will sup...
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                      Hays Wavre - Brabant Flamand(8 days ago)
                      * Quality Event and Risk Management * GCP/GLP/GMP * Belgium, Flemish Brabant area Hays Life Sciences is looking for a Clinical Quality Systems Analyst - GCP (Good Clinical Practice) & GLP (Good Laboratory Practice) to join the Quality Assurance team in a global clinical contract research organization. As a Quality Systems Analyst, you will be responsible for facilitating management of Quality Even...
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                      Arcq - 3020, Herent(8 days ago)
                      Job content You manage clinical trials from start to finish: you carry out pre-study visits, you initiate the trial, you are responsible for routine monitoring and closing visits about the quality standards and timelines You obtain and update essential documentation in compliance with ICH-GCP, Procedural Documents and local regulations both in a Trial Master File (eTMF) and Investigator Study File...
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                      proselect - 4000, Liege(4 days ago)
                      Notre client est un acteur international incontournable dans la production et la distribution de produits industriels divers. Afin de renforcer ses équipes, notre mandant allie sa renommée aux services de proselect pour trouver son futur : Sustainable Product Support (H/F/X) Votre mission : Véritable expert en analyse du cycle de vie ! En tant que Sustainable Product Support votre rôle premier est...
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                      Arcq - 1800, Vilvoorde(9 days ago)
                      Job content Verification of the compliance of the Summary of Product Characteristics, the leaflets and their translations: Signs the “Declaration of Conformity” for registration of variations on a marketing authorization Gives final approval on advertising projects Oversees the training of medicinal representatives to doctor or pharmacist, healthcare professionals. Ensures compliances of regulatio...
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                      Data Scientist About Touring Assurances Member of the Axa Group within AXA Global Direct, Touring Assurances is market leader in direct insurance in Belgium. Every day, our 160 staff are on hand to guarantee a quality and personalised service for our 150,000 customers and our partners. Touring Assurances today remains a company that operates on a human scale. At its offices in the Tour & Taxis bui...
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