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4 resultaten voor Arboadviseur/euse in Steenokkerzeel binnen een straal van 30 km
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Voor de site in Langemark zoeken we een HSE Manager die strategisch denkt én zelf op de vloer staat.
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Brussels Airport Company * Brussels * Vast contract, onbepaalde tijd * Thuiswerken mogelijk - Introductie - Be part of our beating heart - Brussels Airport wil bekend staan als een van de beste luchthavens ter wereld, een volledig verbonden economische hub voor mensen en bedrijven, het kloppende hart van Europa, waar klanten, innovatie en duurzaamheid centraal staan. Wil jij de luchthaven van vandaag en morgen helpen vormgeven? Stop met dromen en kom ons team versterken! Om ons departement HR & Corporate Affairs te versterken, zijn we op zoek naar een H&S Coordination & Optimisation Officer. Ben jij een gedreven Health & Safety medewerker met een passie voor een veilige werkplek? Wil je impact maken op een dynamische luchthavenomgeving en bijdragen aan een cultuur van veiligheid en welzijn? Dan ben jij de H&S Coordination & Optimisation Officer die we zoeken!
Être un support HSE pour l'Engineering dans les gaps assessment Safety by design des activités à haut risques * Apporter un soutien à l'Engineering pour assurer un environnement optimal de santé et de sécurité et Bien-être pour les employés, la sécurité des équipements et des processus allant au-delà de la conformité (directives et exigences HSE et exigences légales). * Être un soutien solide au-delà d'un conseiller, dans la conduite d'une culture HSE positive et orientée vers l'action
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Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Contracting – Walloon – Brabant - Your responsibilities * Writing and monitoring risk assessments for impurities (eg, justification of specifications, elemental impurities risk assessments, extractables and leachables, degradation products, ICH M7-compliant evaluations, etc.) * Planning, coordinating and monitoring the conduct of toxicology studies at contract research organizations in line with project timelines and budget * Performing and monitoring toxicological risk assessments for various health-based exposure limits (PDEs, ADIs, etc.) * Performing and monitoring environmental risk assessments (ERAs) and oversee the conduction of environmental studies to support such assessments. * Authoring and/or reviewing reports, protocols, guidelines, guidances and SOPs and ensuring harmonized ap
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Active member of Lab Quality meetings: act as strong and project. * Be responsible for metrology aspect: Ensure mapping and reports delivered by the External vendors are compliant with the specificities defined by the Lab. * Assures accurate collection and processing of biological specimens to assure quality of analytical data. * Integrate and monitor quality indicators (key performance indicator = KPI), handle non-conformities and claims as well as corrective and preventive actions. Jefferson Wells * Brussels * Contract duration unspecified * Full Time - Brussels – contracting - Your responsibilities * Lead Equipment management process * Be the SME on that process for the entire unit * Train the from equipment purchase to equipment installed. * Ensure at least 1 internal Audit/year.
Support the increase in laboratory capacity with a team of nearly 50 people, including analysts and specialists. Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Cross-Functional Coordination: Work with (TL) to manage deviations, investigations, and priorities. Ensure smooth communication with different teams, especially during urgent situations. * Sample Management: Track samples using tools like LIMS, coordinate their reception, testing, and release, while ensuring compliance with client deadlines. * Deviations and Investigations: Manage deviations, root cause analyses, investigations, and changes related to processes. Precision in managing these tasks is crucial. * Documentation: Manage documentation related to validations, analyses, and regulatory authority r
Active member of Lab Quality meetings: act as strong and project. * Be responsible for metrology aspect: Ensure mapping and reports delivered by the External vendors are compliant with the specificities defined by the Lab. * Assures accurate collection and processing of biological specimens to assure quality of analytical data. * Integrate and monitor quality indicators (key performance indicator = KPI), handle non-conformities and claims as well as corrective and preventive actions. Jefferson Wells * Brussels * Contract duration unspecified * Full Time - Brussels – contracting - Your responsibilities * Lead Equipment management process * Be the SME on that process for the entire unit * Train the from equipment purchase to equipment installed. * Ensure at least 1 internal Audit/year.
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Research Scientist in Histology and Image Analysis for Neurodegenerative Diseases
Research Scientist in Histology and Image Analysis for Neurodegenerative Diseases
Jefferson Wells
Braine-l'Alleud
Jefferson Wells * Braine-l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting - Brabant-Walloon - Vos responsabilités * Performing immunohistochemistry on brain sections, high-throughput image acquisitions using different microscopy instruments, and image analyses using advanced technologies such as artificial intelligence. * Regular interaction with and from different departments within the company, as well as with external organizations, to organize studies and ensure their completion. * Interpreting data and reporting results in an organized and timely manner. * Performing other duties as required and assigned. * Knowledge in neuroscience and neuroanatomy is preferred (rodent, monkey, or human brain). * Expertise in immunohistochemistry (fluorescent, colorimetric) and general knowledge in the field of histology with at least 2 years of experienc
Partner with QA and CMC Development/DCS colleagues to identify and mitigate Compliance risks, resolve potential regulatory observations. * 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. * Coordinate the development local instructions, liaise with key stakeholders in order to maintain common practices with regards to “issued copy” within development enti
Expertise in lab relocation is a plus - Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Lead and coordinate the laboratory expansion and modernization project. * Manage commissioning and qualification activities for equipment and installations. * Collaborate closely with various internal departments and international . * Ensure compliance of facilities and processes with regulatory standards (GMP Pharma). * Identify technical needs and propose appropriate solutions. * Monitor project progress, manage risks, and maintain regular communication with . Votre profil * Bachelor degree with 5 years of relevant experience or Master's degree with 3 years of relevant experience; degree in science, engineering, or a related field. * Pharma skills (change request, deviation
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Omdat we nog veel meer willen verdiepen en verrijken, kijken we voor deze divisie op ons hoofdkantoor in Antwerpen uit naar een bevlogen Auditor QSE. - “Knowledge is Key”, na een aantal opleidingsdagen op het hoofdkantoor vergezel je de lead auditor om je vers opgedane kennis om te zetten in “the field”. SGS Group Belgium * Antwerpen * Vast contract, onbepaalde tijd * Voltijds - Bedrijfsomschrijving - Bij SGS kan je kiezen. Allereerst uit onze verschillende vacatures. Maar je hebt bij SGS nog een andere keuze. Kies je voor verdiepen of kies je voor verrijken? We zijn niet alleen op zoek naar collega's die de diepte van hun vakgebied ingaan. We zijn net zo hard op zoek naar verbinders, collega's die onze indrukwekkende diversiteit aan diensten kunnen koppelen. Aan elkaar. En daarmee onze dienstverlening verrijken. SGS is wereldleider a
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Execution of routine analytical experiments and method development activities under supervision. * Follow established procedures and protocols. * Collaborate with in routine tasks. * Seek guidance for troubleshooting and problem-solving. * Decision-making, primarily under supervision. * Follows standard protocols under supervision. Identifies issues with guidance. * Support and assist in project/operation planning, data analysis, and coordination. * Follows project/operational plans and guidelines. * Assists in project tasks under supervision. * Collaborates with and provides status updates. * Sample management (availability in lab, shipment and reception). * Day to day lab experiment/resources planning and equipment booking in GT
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. * 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. * Participation in the transfer of chemical processes from laboratory to kilo-lab, pilot plant and/or production, under the direction of Science lead. * Knowledge in
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. * Proficiency in analytical techniques (HPLC, UPLC, etc.). * Previous experience in stability or analytical validation (an asset). Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * Write stability and comparability protocols and reports. * Analyze and review scientific data to identify potential outliers. * Ensure data consistency and accuracy before submission to regulatory authorities. * Collaborate with and external . * Contribute to the continuous impro
Jefferson Wells * Braine-l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Walloon Brabant - Vos responsabilités * 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 * Work autonomous, well-organized and use your pro-active thinking skills * Be self-reflective on the gathered data * Use your creativity to develop new analytical methods or even develop new technology * Drive team spirit and encourage collaboration * 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
We will be your career partner for each step along the way. 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
Technical expert in the establishment of robust, fit for purpose injectable drug product manufacturing processes from toxicology studies or first in human until BLA approval. * Define and select drug product manufacturing processes and parameters for clinical manufacture. * Design DP processes for sterile injectable drug products in liquid or lyophilized powder form, in vials, pre-filled syringes or as combination products). * Define the investigational medicine product preparation process in clinical trials. * Provide support to process performance qualification/validation Ensure products are manufactured in accordance with the company quality system, cGMP and latest regulatory requi
Om ons departement Strategy & PMO te versterken, zijn we op zoek naar een Environmental Compliance Manager. De Environment Compliance Manager ontwikkelt de langetermijnstrategie binnen zijn of haar vakgebied. * Je neemt de eindverantwoordelijkheid op voor jouw bevoegdheidsdomeinen en de resultaten van het Environment Compliance Team. * Jij zorgt ervoor dat alle compliance-activiteiten correct worden uitgevoerd, volledig in lijn met het wettelijk kader en het ISO 14.001-zorgsysteem (met uitzondering van geluid). * Samen met je rechtstreekse binnen het Compliance team vorm je een sterk team en werk je nauw samen met het Team Sustainability. * De milieudomeinen waar jij de compliance voor beheert, omvatten onder andere: energiebeheer, luchtkwaliteit, mat
SME Support: Provide technical expertise as needed in engineering and processes, especially in IT, data security, and automation. Jefferson Wells * Braine-l'Alleud * Contract duration unspecified * Full Time - Contracting – Walloon Brabant - Your responsibilities * Project Management: Coordinate a portfolio of projects (mainly in secondary packaging and medical devices), ensuring proper management of schedules and critical milestones. * Inter-project Coordination: Link technical teams, production, and experts (IT, automation) across different departments. * IT/Automation Project Oversight: Manage projects related to Data Integrity, IT security, and the automation of manufacturing facilities. Your profile * Project Management Skills (tools like MS Project). * Technical Knowledge in engineering, particularly in pharmaceutical production (secondary packa
Jefferson Wells * Braine l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting – Brabant Wallon - Vos responsabilités * S'assurer du respect cGMP. * Participer activement à la préparation des lots de process performance qualification (PPQ). * Revoir et approuver les dossiers de lot de production en version papier et électronique. * Participer à la gestion/revue/approbation des déviations. * Participer à la gestion/revue/approbation des CAPA. * Participer à la gestion/revue/approbation des change controls. * Revoir et approuver les protocoles et rapports de validation (CIP/SIP/EM/Thermal mapping). * S'assurer que les risques/non conformités identifiées sont traités de manières adéquates et remontés dans les temps. Votre profil * Diplômé(e) de l'enseignement supérieur de type Bachelier ou Master (biotechnologie, pharmacie, etc.). * Bilingue Français e
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SGS Group Belgium * Antwerpen * Vast contract, onbepaalde tijd * Voltijds - Bedrijfsomschrijving - When you need to be sure, dat is waar SGS voor staat. Bij SGS bieden wij jou namelijk double layer sureness, dubbellaagse zekerheid. Als wereldleider op het gebied van inspectie, controle, analyse en certificering, staan wij garant voor kwaliteit en integriteit. Wereldwijd telt de SGS-familie bijna 100.000 enthousiaste medewerkers. In België geven ca 1900 collega's dagelijks het beste van zichzelf om onze klanten zo efficiënt en professioneel mogelijk verder te helpen. SGS heeft een indrukwekkende diversiteit aan diensten. Binnen onze divisie Industries & Environment hebben we o.a. een toonaangevend advies- en studiebureau dat gespecialiseerd is op het vlak van industrieel milieubeleid en veiligheidsstudies. We zoeken dus naar constructieve oplossingen en adviseren onze
Jefferson Wells * Braine-l'Alleud * Contrat fixe à durée indéterminée * Plein temps - Contracting - Brabant-Walloon - Vos responsabilités * Rédiger et mettre à jour les documents liés à la CCS * Organiser proactivement des réunions afin de collecter les informations auprès des * différents stakeholders (Production, Validation, Maintenance, Qualité, QC, MSAT…) * Développer un visuel afin de faire ressortir les éléments clés de la CCS (draft existant). * Ces documents doivent être finalisés pour l'inspection AFMPS de Juin. * Être en ordre de formation pour les activités dans le scope * Remonter tout problème significatif qui pourrait présenter un risque (qualité, coût, timing…). * Communiquer avec l'ensemble des pour assurer un mode de travail * coopératif. * Supporter les activités requises par le projet. Votre profil * Master * Bonnes connaissances des requis règlemen
Work collaboratively as part of a wider team and when required deputise for the of Bio MSAT Quality and other Bio MSAT Quality Leads * Process industrialization and Technical transfers within commercial manufacturing facilities * Build, establish and develop a governance model and process for Quality oversight of Internal and External MSAT for Bio Drug Substance and Drug Products which fosters continuous quality process improvement, optimized resource utilization and key indicator based performance monitoring * Promote quality best practices throughout the External & Clinical Supply Quality team and where possible business stakeholders. * Knowledge in multiple areas of Biopharma incl manufacturing and analytical testing, including the
Work closely with Clinical Manufacturing Teams to ensure 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. * More specifically, provide quality support for qualification and validation activities related to Clinical Manufacturing activities like facilities cleaning processes, viable and non-viable environmental monitoring, equipment and system qualification/validation - Ensure adequate documentation processes and systems are available and followed for development projects (SOPs / Protocols / Report review…) * Be partner with other departments to identify, mitigate and subsequently resolve complianc
As a Drug Product Expert, you will act as key enabler supporting the advancement of Pharma Science's Science & Technology and Innovation projects by leveraging own area of expertise to functional initiatives and contribute to PS transversal initiatives. * 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 ensure process robustness, validation and transfer of NCEs and Lifecycle management of mature product manufacturing process and technologies to commercial launch site. * To perform clinical formulation orientation work in collaboration with Non-Clinical Formula