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27 ofert pracy dla: Senior Project Manager lokalizacja: Belgia

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  • DescriptionInternational commercial project that focuses on the implementation of a new medical product within the EU. As a project manager you are coordinating this entire process; from design phase to full country roll-out and implementationResponsibilities-The candidate should be extremely comfortable in coordinating

  • Coordinate large and complex commercial projects from design phase to full country roll-out and implementation- Work cross functionally with IT, Finance, HR, R&D- Influence and discuss with senior commercial leaders - Lead a cross functional projectRequirements- Experience as a Project Manager- Excellent

  • regulatory submissions, coordinating all aspects of paper and electronic regulatory submissions- Stay up to date with regulatory requirements relevant for company products- Participate as an active team member and provide strategic regulatory advice to cross-functional program and project teams as required

  • senior manager that coordinates the regulatory affairs in medicinal products, medical devices and dietary supplements.You will be part of a team of several R&D project leaders that work on projects in dermatology, cough & cold, insect & parasite control and other OTC indications.ResponsibilitiesThe ideal

  • and Information Technology organisation, based in Antwerpen Belgium.The CompanyProduces large volumes of data on a daily basis and collaborates with most of the top 20 pharmaceutical companies.Role DescriptionAs project manager it is your job to successfully set-up and initiate projects together

  • seniority you will advise the company how to improve on Quality matters. It is your mission to train the current QA Specialist to manager level.In case you obtain a Belgium QP number, you will help the current QP with batch release.Responsibilities- Mentorship for current QA team. Train current QA

  • a project of 6 months, you as a senior regulatory affairs officer will be involved in the preparation of regulatory submission and ensure that these are followed up and are updated in the system.Responsibilities- Responsible for creating regulatory submissions - Provide detailed product information - Ensure

  • and reinforcing their local marketing organizations.Role DescriptionThe RA Team has responsibility for approving and renewing active substances at EU level and for the processing of applications in the EMEA region.ResponsibilitiesSubstance: provide assistance to the (Senior) Registration

  • results and/or activities and you will write analytical SOP’s and other documentation (protocols, reports, logbooks);- You will prepare technical reports and you are able to independently communicate results, presents and defends own work at meetings. You will also deliver updates to senior level

  • The company is an economic and socially important actor that is aware of its responsibilities and in Belgium puts more than 1. 300 people to work and generates around 4. 000 indirect jobs.Role DescriptionAs an interim Reg. Affairs Manager you will find the perfect mix between quality and result-focus

  • and FMCG organisation, based in Antwerpen Belgium.The CompanyVoor een farmaceutische klant in Geel zijn wij op zoek naar een Quality Manager Manufacturing. Het bedrijf is produceert OTC producten waaronder zalven crèmes.Role DescriptionAls Quality Manager Manufacturing ben je verantwoordelijk voor

  • een aansturing geven aan 12 indirecte reports van u.Responsibilities- U zal optreden als project manager voor nieuwe internationale projecten- U bent het contactpersoon voor externe en internationale klanten- U zal kwaliteitsbesef creëren in de organisatie- U zal een internationaal team van experts

  • organisation, based in Brussels Hoofdstedelijk Gewest Belgium.The CompanyOur client is a professional Pharmaceutical organization, based in Brussel Belgium. As a worldwide leader supplying the pharmaceutical and biotechnology industries with biopharmaceuticals.Role DescriptionAs a regulatory affairs manager you

  • Affairs / team Registratie wordt er een senior RA Manager gezocht. De ideale kandidaat is een ervaren Regulatory Affairs professional, is drie talig en heeft commercieel inzicht. Je werkt grotendeels vanuit huis / België maar bezoekt regelmatig Nederland voor afstemming en aansluiting met het NL

  • developing product trials;Interpreting trial data;Advising scientists and manufacturers on regulatory requirements;Preparing and co-ordinating documentation;Project managing teams of colleagues involved with the development of new products;RequirementsBusiness development skill sets, with exposure to, or

  • Devices organisation, based in Antwerpen Belgium.The CompanyOur client is engaged in the development and production of imaging devices.Role DescriptionThe R&D Manager holds responsibility for the global activities of the R&D organization, participates to the R&D strategy, as well as the budget for R&D

  • Devices organisation, based in Antwerpen Belgium.The CompanyOur client is engaged in the development and production of imaging devices.Role DescriptionThe R&D Manager holds responsibility for the global activities of the R&D organization, participates to the R&D strategy, as well as the budget for R&D

  • Devices organisation, based in Antwerpen Belgium.The CompanyThey are a global organization that focuses on discovering and developing new applications.Role DescriptionThe R&D Manager ensures that the work within R&D is performed efficiently and effectively. This requires clearly defined roles ...

Czy chcesz otrzymywać podobne oferty pracy - "Senior Project Manager", w miejscowości "Belgia" na email?

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