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41 resultaten voor Business development manager in Waals Brabant binnen een straal van 30 km
We hebben je zoekopdracht uitgebreid met 41 gelijkaardige vacatures.
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Nous sommes à la recherche d'un(e) HR Business Partner prêt(e) pour la prochaine étape de sa carrière. Vous travaillez au cœur du département des ressources humaines et jouez un rôle clé dans l'accompagnement des collaborateurs et des managers. * Accompagnement des managers dans le développement de leurs équipes (formations, gestion des compétences, entretiens de fonctionnement,...)
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Participer régulièrement à des réunions de briefing internes avec votre équipe de Business Development et les équipes de support - Au sein de la BU WIND and SOLAR Europe d'un Groupe producteur d'énergies renouvelables, sous la responsabilité de « Belgique » vous occuperez le poste de Business Developer Wind Belgique (H/F). * Développer les projets éoliens depuis la validation du business plan jusqu'au stade « Ready To Build », en vous appuyant sur l'équipe des ingénieurs d'étude et sur l'équipe de Project Management * Assurer le reporting de vos activités au Head of Development
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Design and execution of lab studies in relation to drug product development activities, capture and analyze data and author related documentation (write-ups, protocols, reports (eg filter selection and sizing, target fill volume assessment, compatibility assessments, clinical blinding, etc). * Support knowledge transfer from late phase development to commercial for validated DP processes. * Minimum 3-5 years experience in sterile liquid drug product development and/or manufacturing within the pharmaceutical industry * Knowledge and technical experience in liquid drug product development and cGMP manufacturing under aseptic conditions (such as vial, cartridge and pre-filled syringe filling) * Technical knowledge of sterile DP development covering DP components, process transfer, scale-
As an Analytical Development – Document Specialist, your mission is to write and review scientific documents related to the stability and comparability of products in clinical development, primarily in phase 3.
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Vous êtes sincère, solide commercialement et avez une expérience concrète en business development auprès de clients professionnels (B2B). En collaboration étroite avec le Sales Wallonie et l'équipe Back Office basée à Herentals, votre mission consiste à poursuivre le développement de votre zone sur base d'un business plan bien réfléchi.
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Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Contracting – Brabant-Walloon - Your responsibilities * Monitor the progress of plans and projects, GQA performance, and compliance through * meaningful KPIs. This will boost operational efficiency and agility. Ensure and track appropriate * data entry performance of audit reports and CAPAs in the Veeva audit system. * Enable insights for the company through data collection, entry, and analysis in the audit * management tool (e.g., trending, KPIs, etc.). * Curate data, including quality checks of audit management tool as needed, for * KPIs/metrics on performance and information on trending. * Ensure maintenance and improvement of quality of critical data within the Quality * Management System (includes data entry of audit related information and data * monitoring).
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Ideally 1 proven track record in business development of digital/high-tech products - In Europe, our Connected and Sharing Solutions Division is currently looking for a Business Developer Automotive to strengthen this team. * Generate lead and create new business model for SW and content * Master's degree in Business, Marketing, Innovation or Engineering
To lead this initiative, we are looking for a dynamic Senior Business Developer to lead business development activities, strengthen market leadership and establish strategic partnerships. Business development * Define and execute the business development strategy for the Belgian C&I market. * B2B experience: Proven track record in B2B business development and sales leadership. As part of our renewables business, C&I Solutions specializes in helping commercial and industrial clients transition to sustainable energy through customized, scalable solutions. Our team works with businesses to implement comprehensive renewable energy systems - from solar installations and wind turbines to EV
Managing distribution processes, designing solutions that meet business and IT needs. * Ensuring smooth communication between business teams and IT departments, especially for market-specific solutions.
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Consultant en Recrutement bilingue - Hays Louvain-la-Neuve
Consultant en Recrutement bilingue - Hays Louvain-la-Neuve
HAYS
Mont-Saint-Guibert
Thuiswerken mogelijk
Louvain-la-Neuve | Consultant en recrutement | Sélection | Life Science | Business Development * Un fort esprit d'entreprise pour gérer votre propre business ? Learning & development
Development of an in-depth understanding of the process chemistry and process engineering relating to the postholder's projects and an awareness of chemical aspects of other projects within the group. * Identification and definition of specific analytical tests in order to facilitate effective process development and ensure optimum product quality. Additional requirement of full compliance with all companies business policies and guidelines. * Knowledge in crystallization process development and characterization * Ability to participate to process development as scientist in specific area of expertise as process characterization, optimization, understanding, industrialization and investigation QbD development of the different compounds in development.
Work in accordance with the company HSE and Corporate policy requirements and drive personal training and development activities to meet the needs of the business and professional career development * Work closely with Global , Technical Operation Teams and Business stakeholders in an effective and efficient way * Promote quality best practices throughout the External & Clinical Supply Quality team and where possible business stakeholders. * Provide support to other and assist in the further development of the wider team * Excellent knowledge of the Bioceutical industry from a business and technical perspective. * Be able to coach/train/mentor colleagues and deliver training within area of expertise and assist with the development of
Support the management of outsourced activities and collaborations within the internal departments (including elements of early development), including interactions and negotiations with external partners such as Contract Research Organisations, consultants, and non-commercial partners. * Implement high-quality contracts ensuring compliance with Legal, Intellectual Property, Procurement, Quality Assurance, Finance, and Ethics and Business Integrity policies, using approved templates. * Excellent time management and organizational skills, with the ability to set priorities according to business needs.
Identify, address, and escalate issues that may impact business operations. * Master the use of SAP within the EMDP business process (R/3, APO). * Bachelor's degree in supply chain management, Logistics, Business Administration, or a related field. * Strong proficiency in SAP (R/3, APO) and related business processes.
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We are looking for a Project Manager to support the development of our hydrogen production projects in Flanders and Wallonia. We combine production development with innovative infrastructure solutions through DATS 24's refuelling network, while actively shaping the hydrogen market by establishing strategic partnerships with off takers. As part of Virya Energy's broader renewable energy portfolio, we leverage the group's extensive experience across the energy sector while maintaining our focused expertise in hydrogen development. * Variety & challenge – Work on diverse projects at different development stages.
PCR method development, qualification, non-GLP sample testing and reporting, to deliver high quality data to advance UCB's gene therapy portfolio * There may be opportunities to support the method development and sample testing for other bioanalytical methods including cell-based immunogenicity assays * Demonstrated advanced technical understanding of PCR assay development and optimization, experience with qPCR and digital PCR technology platforms is a plus
Coordinate inspections or audits by regulatory authorities, companies Global Quality Auditing team, and others as needed (including development of responses). * Additional Skills: Demonstrated experience in biological drug substance (business and/or quality) to facilitate interactions with other teams.
The GSP oversight (non- GMP activities) of different development entities, located on the Braine site (BE), the Slough site (UK) and the Monheim site (DE). * Drive continuous quality improvement process, ensuring that the Quality Management System in support of product development and clinical supplies, work in a way that ensure product quality, safety and efficacy, meet regulatory requirements and expectations and operate in a fit for purpose and in a smarter way. * Identify, mitigate and subsequently resolve compliance and quality issues that may affect company development activities and products. * Ensure adequate for the qualification, validation and maintenance of the equipment, classified rooms, HVAC used in development manufacturing areas or laboratories, as well as related cleaning validations
Senior expert in clinical DP development accountable for leading and running assigned project work packages, ranging from clinical formulation orientation work for FIH study up to commercial registration and launch for the development pipeline and as part of the life cycle management of commercial brands. * To drive development (internal or external) of innovative formulations and manufacturing processes for the supply of bulk clinical trial material for development pipeline projects. DS/DP clinical campaigns, DS & DP process optimization, analytical method development & validation, stability program, route evaluation, form selection, material characterization, … * Design experiments/trials and studies in accordance with Operating Model to support projects DS, DP or analytical
Work in accordance with the company HSE and Corporate policy requirements and drive personal training and development activities to meet the needs of the business and professional career development. Perform the QA review of deviation notifications, retrieve and collect supportive information from involved stakeholders (the company Vendor Team, GQL, ILA, ALO, Business) to allow assessment. Has good background knowledge of the pharmaceutical industry from a business and technical perspective.
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The power of people and positivity is at the heart of our business. We reinvest our profits into research and development, helping to lower the cost of participating in sport.
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Interogo Foundation aspires to use our influence to empower people, organisations and businesses to do good for the people and the planet, while growing our assets responsibly. As Technical IT Security Manager you maintain and evolve the (technical) security infrastructure and controls, you oversee operational topics and incident management, and you manage relevant security governance tasks. You hold a critical role in translating group-wide IT security projects into practice and align security measures with business risks and compliance standards. The Technical IT Security Manager is part of the IT team, works closely with the external and Information Security Officer (CISO), and reports to the . You participate in continuous learning and professional development to maintain expertis
Execution of routine analytical experiments and method development activities under supervision. * All these activities will be performed in respect of the material and premises, in compliance with the HSE/Biosafety/GSP or GMP rules and with the regulatory requirements for each development phase of the product. * Previous development or validation of methods for viral vector products is a plus. * Knowledge of statistical tools supporting the development/characterization of reliable analytical methods.
Collaborate with IT and business teams to guarantee data accuracy and consistency. * Communicate with various (IT, Business, QA, QC).
Participate to the development of new products and processes * Give directions from early development up to lifecycle management, from particle design up to final product * Being a leader in powder characterization by leveraging Materials Science to drive overall Product Development in order to obtain the right drug for every patient * Guide the Product Development by connecting powder /particle insights with manufacturing technologies and overall product performance * Applying QbD principles, multivariate analyses, and being in support of PAT development