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8 jobs voor Sales Support gevonden in Leuven (3000)

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CRM Application Specialist

SYNERGIE LEUVEN in LEUVEN
time Online sinds 19 juli 2024 - Vaste jobs

As a CRM Application Specialist, your tasks will include:

  • Administering and configuring CRM systems, including Salesforce and legacy Dot.Net applications, to support business processes and workflows;
  • Managing user access, security settings, and data integrity within the CRM platforms;
  • Implementing customizations and enhancements to meet evolving business requirements, leveraging your expertise in CRM technologies;
  • Providing ongoing support and troubleshooting assistance to users, addressing inquiries, resolving issues, and ensuring optimal system utilization;
  • Developing and delivering training programs and materials to educate users on CRM functionalities, best practices and updates;
  • Acting as a liaison between end-users and technical teams, facilitating communication and driving resolution of user issues;
  • Collaborating with stakeholders to gather requirements, assessing system performance, and identifying opportunities for optimization;
  • Recommending and implementing enhancements to CRM systems, such as workflow automations, custom reports, and dashboards, to improve efficiency and productivity;
  • staying informed about industry trends and best practices in CRM technology, proactively suggesting improvements and innovations;
  • Participating in CRM-related projects, including system upgrades, migrations, integrations, and new implementations;
  • Working closely with cross-functional teams, including sales, marketing, and IT, to define project scope, requirements and timelines;
  • Coordinating with internal resources and external vendors/consultants to ensure successful project delivery, support, and adherence to quality standards;
  • Overseeing the performance of vendors, ensuring alignment with project objectives, timelines and budgetary constraints.

Bedrijfsprofiel:

As a CRM Application Specialist, you will play a crucial role in managing, optimizing, developing, and supporting our organization's CRM.Do you have a blend of technical experience, project management skills and a deep understanding of business needs, and are you ready to be a part of a pioneering company at the forefront of dental technology?Then you might be the person we're looking for!

Technical Service Administrator (M/V/D)

AVANTOR SCIENCES in LEUVEN
time Online sinds 20 juli 2024 - Vaste jobs
Als Technical Service Coordinator plan je de agenda's van de techniekers in zodat zij zo efficiënt mogelijk te werk kunnen gaan en coördineer je de aanvragen van onze klanten van A tot Z.
Je werkt binnen deze functie van maandag tot en met vrijdag, 38u/week.
We bieden een tijdelijk contract van 1 jaar.Naast een competitief salaris bieden we extralegale voordelen waaronder hospitalisatieverzekering, groepsverzekering en maaltijdcheques.

In deze functie werk je binnen onze Equipment Services afdeling van Avantor die bestaat uit enerzijds een groep van Field Service Engineers die verantwoordelijk zijn voor de installatie, het preventief onderhoud en de herstelling van een uitgebreid gamma van laboratoriumapparatuur, en anderzijds een team van Technical Service Coordinators die instaan voor de administratieve opvolging van deze dienstverlening.

Hoe je zal groeien en een impact zal maken
  • Je staat in voor het inplannen, coördineren en opvolgen van interventies van de Field Service Engineers.
  • Je bent de sleutelpersoon tussen klant, techniekers, sales team en leveranciers.Je zorgt voor een vlotte communicatie en samenwerking met de verschillende betrokken partijen.
  • Je communiceert proactief met klanten om interventies in te plannen en volgt deze op van het maken van de offerte tot de aanzet voor de factuur na de uitvoering.
  • Je speelt een actieve rol in het analyseren en verbeteren van bestaande processen.

Clinical regulatory affairs specialist

SYNERGIE LEUVEN in LEUVEN
time Online sinds 19 juli 2024 - Vaste jobs

What will your main tasks be?

  • Prepare and update clinical evaluation plans and reports (CERs) for Class III medical devices;
  • Liaise with internal and external stakeholders to ensure timely completion of CERs;
  • Prepare and update PMS plans, periodic safety update reports (PSURs), post-market clinical follow-up (PMCF) plans and reports, and summaries of safety and clinical performance (SSCPs) for Class III medical devices;
  • Conduct clinical literature and vigilance database searches;
  • Conduct PMCF studies (e.g.surveys) and collaborate with the Product Management Department or support consultants conducting such studies;
  • Implement scientifically and statistically sound methods into study plans and data analyses;
  • Participate in the design, management and reporting of clinical investigations as required;
  • Liaise with Sales, Marketing and QA Departments to ensure PMS activities are conducted under regulatory supervision;
  • Ensure relevant CE marking documents, including product technical files, are complete and up to date;
  • Perform vigilance activities as required.

You will also have to ensure that the organisation consistently meets legal obligations, focusing on:

  • Compliance with the Medical Device Regulation (MDR) for Class III medical devices;
  • Clinical evaluation requirements under the MDR;
  • Post-market surveillance (PMS) requirements under the MDR.

Bedrijfsprofiel:

Join a leading innovator in the dental industry as a Clinical Regulatory Affairs Specialist.Do you want to advance your career with a globally recognized company known for its high-quality products, and already have some experience in clinical research and medical writing?Then this role is perfect for you!