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10 resultaten voor Wetenschap in Fleurus binnen een straal van 30 km
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BASF Belgium Coordination Center N.V * Waterloo * Vast contract, onbepaalde tijd * Voltijds - As an EHS Specialist, you are part of the EHS Service organization of the Benelux, consisting of 3 people. In this position, you are one of the experts for the themes of safety, health and the environment. It concerns a role for 32 hours per week. Jouw verantwoordelijkheden * Acting as prevention adviser for our various sites (Waterloo, Brussels, Gembloux). * Developing, implementing and evaluating the well-being policy, in accordance with the Dynamic Risk Management System referred to in the KB Well-being Policy. * Coordinating the activities and obligations as a local point of contact for Belgian public authorities (Valipac, FAMHP, FASFC). * Performing and supervising EHS inspections and audits (at the BASF Benelux locations).
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Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Contracting – Braine-l'Alleud - Our partner is looking for an In vivo Principal Scientist to join its teams. This international company is well known for its pharmaceutical products. Your responsibilities * Collaborate across project teams to establish scientific in vivo strategy and study plans for drug discovery projects. * Serve as the in vivo pharmacology lead for several drug discovery projects. Ensure that projects have all critical in vivo data to enable project stage dependent decisions. * Work within multi-functional teams to support target identification, validation within the drug discovery process. * Work across the in vivo team in a highly collaborative manner, sharing expertise and resources to meet study needs across In Vivo Pharmacology.
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Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * New primary packaging systems development management in line with the strategy, “Pipeline Devices & Delivery Systems” and technologic/scientific platforms objectives and according to established working processes. * Clinical medical devices design and assessment * Primary packaging systems sustaining and life cycle management coordination and support to all operation sites and CMO's. * Competitors primary packaging systems portfolio analyze & characterization. * Primary packaging materials, components and technology scouting and assessment according to defined priorities * Planning, implementation and documentation to maintain and set up the systems (processes, resources, equipment) of the organizational unit
Jefferson Wells * Wavre * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Ensuring that Quality systems are in place/in use, routinely monitored and assessed * Mastering quality agreement content * Releasing validation and/or commercial batches, including production and Quality control documentation, within the time frame defined by submission or Market needs and in compliance with regulatory files, good manufacturing practices and regulatory requirements, certify release process and evaluate regularly the certification status * Ensuring all quality activities linked to the contractor / supplier management (deviations, CAPA closure, change control, risks management, complaints, product quality review, …) * Ensuring and maintain good relationships with the in order to guarantee win-win collaboration, through inform
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Audit Management * Conduct audits of Study Reports, Study Phase Reports, Study Plans and Study Plan Amendments to assure the applicable OECD guidelines, SOPs and the Analytical Methods have been adhered to and that reported results accurately reflect the raw data according to SOPs and associated controlled documents * Archive audit documentation per SOPs; e.g., issued audit reports, supporting documentation, QAS, additional documents as expected according to SOPs and associated controlled documents * Follow up with CAPA to manage actions to an on-time completion according to SOPs and associated controlled documents Issue Management * Contribute to investigations of non-compliance to areas of research and development operations whic
Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Brabant Walloon – Contracting - Our partner is currently looking for a CMC Quality Solutions Specialist. Our partner is an international pharmaceutical company. Your responsibilities * Product Change Control Committee preparation and change controls follow-up * Maintenance and lifecycle management of QA product flows * Audits and Inspection anticipation and readiness * Product metrics * Review of Annual Stability Plan * SOPs and other control documents writing, review and approval as needed * Building and maintenance of Product QA knowledge (i.e., Product(s) SharePoint(s)) * Risk management and mitigation if applicable (e.g., follow-up on risk actions with QA stakeholders) * Review and approval of CMC sections linked to regulatory original submissions, renewals or variations during any mom
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Be the central QA point of contact for the organization for investigations/deviations/ out-of-specifications/ audit observations associated with the assigned vendors. Perform the QA review of deviation notifications, retrieve and collect supportive information from involved stakeholders (Vendor Team, GQL, CAS, Business) to allow assessment. * Manage the key performance indicators (metrics) for key operational QA activities and services associated with the vendors in the defined described tracking tools ( QA KPI tracker, QuickScore) and track the 's performance * Ensure all Quality agreements are in place and take ownership of agreements for the vendors. Maintain Quality Agreement with the vendors up to date and perform periodic rev
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SGS Group Belgium * Wavre * Contract duration unspecified * Full Time - Company Description - SGS is the world's leading inspection, verification, testing and certification company. We're also the benchmark worldwide for quality and integrity. And that makes us very proud. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise. Job Description - As Business Development Manager you will be responsible for identifying and exploring strategic business development opportunities within the Bioanalysis division to maximize organization growth. * Actively prospecting new customers and new business opportunities worldwide and develop new opportunities with existing clients on Preclinical (GLP) and Clinical (GCLP) Bioanalytical projects. with your
Optibi BV * HOEILAART * Freelance * Deeltijds Jouw verantwoordelijkheden * Je begeleidt in het middelbaar bij de wetenschapsvakken (wiskunde, biologie, fysica, chemie en/of natuurwetenschappen). * Lesgeven doe je op locatie (bij jou thuis of bij de student thuis) of via onze gratis online leeromgeving. * Je geeft les op momenten die voor jou goed passen in overleg met de . Jouw profiel * Je bent een bachelor- of masterstudent, of hebt reeds een diploma hoger onderwijs op zak. * Je hebt een diepgaande kennis van minstens één van deze vakken en je kan deze kennis overzichtelijk overbrengen bij anderen. * Je bent een krak in je vak, geduldig en verantwoordelijk. * Leservaring is een pluspunt, maar niet vereist. Location Optibi BV1560 HOEILAART, België
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SGS Group Belgium * Wavre * Contrat fixe à durée indéterminée * Plein temps - Description de l'entreprise - SGS is the world's leading inspection, verification, testing and certification company. SGS Life Sciences is a leading contract research organization offering Clinical Research Drug Development and Quality Control/Laboratory Testing Services to the pharmaceutical and biopharmaceutical industry. It provides outsourcing services on both the quality and safety of drug ingredients and the drug development process – from the early development stages until the commercialization of the finished product. To strengthen our Business IT team, we are currently looking for a Business IT manager – CSV - Description du poste * Create detailed project planning and . * Establish and follow the budget. * Coordinate and follow all project tasks and make sure progresses are made.
We hebben je zoekopdracht uitgebreid met 2 vacatures buiten de geselecteerde regio
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Diploma: Je beschikt over een Master in de Industriële Wetenschappen - Elektromechanica.
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Delta Light * Belgium * Contract duration unspecified * Full Time - Delta Light HQ - Wevelgem - Möchten Sie Teil eines international tätigen Unternehmens mit fantastischen KollegInnen werden, in dem Ihre Ideen gehört und Ihre Talente gefördert werden? Klicken Sie hier, um sich direkt zu bewerben. Gesellschaft >Incorporated in Belgium in 1989 by business manager and designer Paul Ameloot, today Deltalight has developed to become the market leader and trendsetter in architectural lighting. Presenting innovative lighting designs, the company is recognised throughout the world for its subtle blend of ambiance, elegance, functionality, and design, both in interior and exterior lighting. The future of Deltalight is guaranteed with Peter and Jan Ameloot joining their father at the helm of the company, bringing additional dynamism and ambition to the team.
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Knowledge of LIMS systems (ideally LabWare). * Previous experience with the LabWare LIMS system. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Act as a between the local team and the global team to integrate new developments and keep documentation and training up to date. * Update training matrices according to new methods and specifications. * Assist in training on new methods and gather their requests and points of attention. * Participate in project meetings and document reviews, and challenge deadlines and training. * Maintain smooth communication between different services and teams. * Manage and rethink the team's document structure to make it more accessible to end users. * Support the drafting of deviations and CAPA depending on worklo
Autonomously manage and execute daily laboratory activities related to method development, validation, and transfers. * Perform all activities in compliance with GMP/HSE rules and regulatory requirements for each development phase of the product. * Expertise in analytical method development and validation. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Design and conduct experiments. * Contribute to release and stability testing in relation to the project, as appropriate. * Prepare, review, and approve documentation (procedures, protocols, reports). * Analyze experimental results. * Verify data accuracy. * Present and discuss results in meetings. Votre profil * Master's or Bachelor's degree in biochemistry or analytical chemist
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Focus on large-scale equipment for the facility. * Package owner : Supplier management, equipment final design, execution and qualification, P&ID tracking, electrical schematics, project execution (planning, coordination,….). Votre profil * Master's degree * Minimum 5 years of experience within pharmaceutical companies and working with Engineering offices * Requires project management experience in pharma, knowledge of qualification, and equipment design. * Experience: Preferably in CAPEX projects within a commercial GMP facility. * Good Upstream
Basic understanding of CSV qualification and automation processes. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Coordinate qualification and validation activities for cleaning equipment (e.g., washers, COP stations). * Manage change controls and deviations using the Viva system (internal training provided). * Support the qualification of new equipment and validation activities by coordinating with production and support teams (e.g., ensuring availability of materials and personnel). * Collaborate with a on Washer and COP/SOP-related activities. * Participate in the review of validation protocols, test sheets, and reports. * Conduct regular on-site follow-ups and coordinate with production and automation teams. * Oversee technical layout aspects (e.g., moving
Pour l'un de nos partenaires, une entreprise pharmaceutique située dans le Brabant Wallon, nous recherchons un Data Reviewer Chimie. * Vous avez de l'expérience soit en tant que data reviewer soit en tant qu'analyste. Alors, si vous êtes orienté data et chimie, la suite va vous plaire ! Jefferson Wells * Wavre * Contrat fixe à durée indéterminée * Plein temps #Wavre #QC #data #revue #pharma - Vos responsabilités - Quelles sont vos responsabilités ? * Effectuer la revue minutieuse des données brutes du laboratoire QC, en veillant à leur précision et à leur conformité aux normes établies. * Éditer les rapports d'essais via le LIMS pour toutes les commandes validées, en garantissant l'intégralité et la qualité des documents générés. * Examiner les canevas de travail, les cahiers de laboratoire et les feuilles de calcul E
Hands-on experience with Electronic Document Management Systems (EDMS), preferably Veeva Vault. * Perform quality control on non-clinical documents (protocols, amendments, reports, etc.). * Ensure compliance and readiness of documents for regulatory submissions. * Upload, index, and track documents in the Veeva Vault EDMS. * Oversee the document lifecycle, ensuring adherence to quality standards and GLP requirements. * Strong background in regulated documentation management (GLP, GCP, etc.). * Familiarity with regulatory requirements for submission-ready documents. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités - Your Responsibilities * Liaise wi
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Senior Business Developer - Sustainable Energy Solutions
Senior Business Developer - Sustainable Energy Solutions
Eoly Energy
Braine l'Alleud
Thuiswerken mogelijk
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. 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 charging infrastructure - while ensuring minimal disruption to their operations and maximum return on investment. Your role will be crucial in understanding each client's unique needs and growth trajectory, creating flexible energy solutions that evolve with their business while maximizing ef
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