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3 results for Hygiene Regulations jobs in Mol within a 30 km radius
No match yet? There are 3 more jobs that could match your search
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Willing to learn new techniques and to work adhering to strict regulations
Willing to learn new techniques and to work adhering to strict regulations
Lead the design of the abatement system, ensuring compliance with all technical specifications, regulatory and safety regulations, including radiation protection and nuclear safety.
Lead the design of the abatement system, ensuring compliance with all technical specifications, regulatory and safety regulations, including radiation protection and nuclear safety.
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You will be assigned to trial sites to ensure compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), as well as applicable regulations and guidelines. Strong proven understanding of GCP, local laws, and regulations
You will be assigned to trial sites to ensure compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), as well as applicable regulations and guidelines. Strong proven understanding of GCP, local laws, and regulations
3 exact matches jobs are outside your preferred location
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Manage export operations, including logistics, documentation, and compliance with regulations. * Proficiency in export regulations and documentation.
Manage export operations, including logistics, documentation, and compliance with regulations. * Proficiency in export regulations and documentation.
Senior Cloud Solution Architect for Sovereign Cloud - Europe North
Senior Cloud Solution Architect for Sovereign Cloud - Europe North
Microsoft
Multiple Locations, Belgium
Deep understanding of cloud architecture, compliance frameworks, and data sovereignty regulations in Europe.
Deep understanding of cloud architecture, compliance frameworks, and data sovereignty regulations in Europe.
Liège Airport Nv * Belgium - Solliciteer als één van de eersten - Job Description - GOOSE are working with an airline who are looking for a CAMO Engineer specialising in Avionics to join their team at Liege Airport Belgium. es. You will be responsible for assisting the continuing airworthiness team with avionics engineering activities and overseeing repairs, modifications and trouble shoot ting. You will follow aircraft configuration and specifications as well as reviewing OEM recommendations. You will provide technical recommendations to the MCC and Part-145 department and input into preventative maintenance proce edures. You will analyse airworthiness directives to develop a compliance plan and interact with OEM's and stake - About you: keholders. You will live within commutable distance of Liege Airport or be willing to relocate and you will hold the right to work
Liège Airport Nv * Belgium - Solliciteer als één van de eersten - Job Description - GOOSE are working with an airline who are looking for a CAMO Engineer specialising in Avionics to join their team at Liege Airport Belgium. es. You will be responsible for assisting the continuing airworthiness team with avionics engineering activities and overseeing repairs, modifications and trouble shoot ting. You will follow aircraft configuration and specifications as well as reviewing OEM recommendations. You will provide technical recommendations to the MCC and Part-145 department and input into preventative maintenance proce edures. You will analyse airworthiness directives to develop a compliance plan and interact with OEM's and stake - About you: keholders. You will live within commutable distance of Liege Airport or be willing to relocate and you will hold the right to work
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KEY 4 Nova Bv * Achel * Vast contract, onbepaalde tijd * Deeltijds - Our client is a leading provider of pharmaceutical packaging solutions, specializing in advanced and innovative services to meet the needs of the pharmaceutical industry. Committed to delivering the highest quality standards, they support clients globally with a range of services, from packaging design to serialisation and clinical trial solutions. With a focus on precision, safety, and compliance, they are trusted worldwide to ensure the utmost quality in each step of the packaging process. Requirements * Is subject matter expert in the field of sterilization; supporting running commercial sterilization processes, as well onboarding new sterilization programs and new sterilization technology. * Acquires and maintains scientific and technological knowledge and background of existing and new pharmaceu
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Hun expertise gaat veel verder en stelt hen in staat de industrie te ondersteunen in elke fase van ontwerp, ontwikkeling, productie en Global QA/RA Director Als Global QA/RA Director ben jij verantwoordelijk voor de aansturing en verdere ontwikkeling van de Quality Assurance afdelingen op de sites in Nederland, België, de UK en de US. Strategische en leidinggevende QA/RA-rol met internationale verantwoordelijkheid binnen een groeiende organisatie (Standplaats bespreekbaar – regelmatige aanwezigheid vereist op o.a. Hamont-Achel, Heerenveen, Rhymney en Bethlehem) * Minimaal 15 jaar relevante werkervaring binnen QA/RA in de farmaceutische industrie; * Aantoonbare ervaring in het aansturen van (internationale) QA/RA-teams
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Jefferson Wells * Braine-l'Alleud, Région wallonne, Belgique * Vast contract, onbepaalde tijd * Voltijds - Contracting – Brabant Wallon - Vos responsabilités - The recruitment is to support a complex issue related to PEG, in collaboration with a . The work involves technical investigations on polymers, with connections between current analyses, methods, and validations. * Follow-up on deviations and quality issues related to PEG. * Analyze and understand unusual results. * Collaborate with regulatory specs, analytical development, method redesigns, transfers, and production. * Participate in quality committees on Tuesdays and Thursdays. * Use analytical techniques (HPLC, GC, IR, NMR) and software tools (Empower, Cromeleon). Votre profil * Pharmaceutical experience (submission files, regulatory knowledge). * Proactivity, autonomy, ability to raise issues and suggest so
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Clinical Applications - Solution Area Specialist - Dutch Speaking
Clinical Applications - Solution Area Specialist - Dutch Speaking
Microsoft
Multiple Locations, Belgium
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We will be your career partner for each step along the way. * Jefferson Wells * Braine-l'Alleud, Région wallonne, Belgique * Vast contract, onbepaalde tijd * Voltijds - Contracting – Brabant Wallon - Vos responsabilités - The role is within the Clinical Supply Quality team, focusing on packaging and labeling for clinical studies. The position is critical for ensuring quality systems and compliance in the production, release, and distribution of Investigational Medicinal Products (IMPs) for clinical trials. - Review of batch records (both electronic and paper). - Review and release of labels. - Release of warehouses and production consumables specification. - Update of CEC (Controlled Environment Conditions). - System-related activities: deviation review, CAPA (Corrective and Preventive Actions), change control. - Temperature excursion management. - Va
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With more than 40,000 employees, working in more than 1000 laboratories and offices worldwide, we are focused on exceeding customer expectations with innovative quality solutions. The laboratory in Antwerp takes care of the production and delivery of laboratory services 24 hours a day, 7 days a week. * Intertek Belgium NV * Antwerpen * Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - Introduction - Intertek is a leading supplier in the field of total quality assurance. The service is characterized by quality and short response times and is ISO 17025 accredited and ISO 9001 certified. Activities include both high-frequency measurements, often with short response times, and measurements with lower frequencies and longer response times on petroleum products, gases and petrochemicals and re
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Doorgroeimogelijkheden richting productiemanager, procescoördinator of continuous improvement. * Enginity * Overpelt * Vast contract, onbepaalde tijd * Voltijds - Onze klant is een toonaangevend bedrijf in de huishoudelijke sector dat bekendstaat om kwaliteit, innovatie en duurzaamheid. Ze ontwerpen en produceren slimme, stijlvolle oplossingen voor dagelijks gebruik, met oog voor zowel functionaliteit als milieu. Hun focus ligt op efficiënte processen, samenwerking en voortdurende verbetering, zodat klanten wereldwijd kunnen vertrouwen op betrouwbare en doordachte producten. Jouw verantwoordelijkheden - Als Productie manager ben je verantwoordelijk voor de dagelijkse operationele werking van een afdeling binnen de productie. Je stuurt een team van 50p aan dat bestaat uit , en . Samen zorg je voor het behalen van de productie- en kwaliteitsdoelstelling
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Oversee and coordinate major projects across the Benelux region, ensuring consistency in delivery and adherence to client-specific standards. Operating internationally, the company is recognized for its commitment to speed, excellence in execution, and rigorous delivery standards across various sectors, including strategic client projects. To oversee the delivery of high-profile projects across the Benelux region, they open a new position of * Act as the primary point of contact for strategic clients on project-related matters. * Implement and enforce Portakabin's project delivery processes, tailored to meet the elevated requirements of international clients. * Identify weaknesses in local project execution and lead improvement initiatives. * Collabor
Oversee and coordinate major projects across the Benelux region, ensuring consistency in delivery and adherence to client-specific standards. Operating internationally, the company is recognized for its commitment to speed, excellence in execution, and rigorous delivery standards across various sectors, including strategic client projects. To oversee the delivery of high-profile projects across the Benelux region, they open a new position of * Act as the primary point of contact for strategic clients on project-related matters. * Implement and enforce Portakabin's project delivery processes, tailored to meet the elevated requirements of international clients. * Identify weaknesses in local project execution and lead improvement initiatives. * Collabor
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We are currently looking for the right person to join our Advanced Quality Engineering Department. * Minimum 2 years automotive experience in advanced quality activities * Acting as a key contact to IEE customers for quality-relevant topics during development and serial production - o Minimizing quality risks * Ensuring that customer quality requirements are known and fulfilled - o Follow up on quality-relevant activities - o Ensuring quality of products * Driving quality activities during the product industrialization phase * Detailed knowledge or relevant quality standards, tools and methods such as ISO 9001, ISO TS16949, VDA 6.3, APQP, FMEA, FTA, risk assessment etc. * IEE S.A. * B
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Nous sommes actuellement à la recherche d'un(e) Analyste en Chimie pour rejoindre nos laboratoires SGS Lab Simon et SGS LCA. * SGS Group Belgium * Wavre * Vast contract, onbepaalde tijd * Voltijds - Snel solliciteren - Description de l'entreprise - SGS est une société internationale d'inspection, de vérification, de testing et de certification. Description du poste * Effectue les essais de conformité sur les matières premières ou produits finis. * Enregistre promptement, précisément et intégralement les données nécessaires à la traçabilité des opérations effectuées conformément aux procédures en vigueur (échantillons, réactifs, appareillages, initiales, dates). * Signale immédiatement tout résultat hors spécification au superviseur de laboratoire conformément à la procédure en vigueur. * Signale au plus vite au Team Leader tout besoin en matériel et r
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If so, we invite you to join our team as a Cloud & AI Solution Engineer in Innovative Data Platform for ISV customers at Microsoft. As an Innovative Data Platform Solution Engineer (SE), you will play a pivotal role in helping enterprises unlock the full potential of Microsoft's cloud database and analytics stack across every stage of deployment. This opportunity will allow you to accelerate your career growth, develop deep business acumen, hone your technical skills, and become adept at solution design and deployment. You'll guide customers through secure, scalable solution design, influence technical decisions, and accelerate database and analytics migration into their deployment workflows. As a trusted technical advisor, you'll guide customers through secure, scalable solution desi
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Jefferson Wells * PUURS * Vast contract, onbepaalde tijd * Voltijds - QC Analyst – Analytical (m/v/x) Contracting – Puurs - Vos responsabilités * Coördineren en plannen van analytische methodeoverdrachten en validaties voor de introductie van nieuwe producten. * Beoordelen van de conformiteit van validatie- en compendiale dossiers. * Implementeren van nieuwe analytische methoden in de QC-operaties in nauwe samenwerking met Analytical R&D. * Opstellen en beoordelen van validatieprotocollen, testscripts, overdrachtsrapporten en afwijkingsrapporten. * Valideren van analytische rekentools (zoals Excel, SoftMaxPro, enz.). * Opleiden en ondersteunen van QC-analisten bij de uitvoering van analysemethoden. * Problemen analyseren en oplossen met behulp van gestructureerde methodieken (DMAIC, root cause analysis). * Mede-auteur zijn van documenten voor regelgevende indieningen
Jefferson Wells * PUURS * Vast contract, onbepaalde tijd * Voltijds - QC Analyst – Analytical (m/v/x) Contracting – Puurs - Vos responsabilités * Coördineren en plannen van analytische methodeoverdrachten en validaties voor de introductie van nieuwe producten. * Beoordelen van de conformiteit van validatie- en compendiale dossiers. * Implementeren van nieuwe analytische methoden in de QC-operaties in nauwe samenwerking met Analytical R&D. * Opstellen en beoordelen van validatieprotocollen, testscripts, overdrachtsrapporten en afwijkingsrapporten. * Valideren van analytische rekentools (zoals Excel, SoftMaxPro, enz.). * Opleiden en ondersteunen van QC-analisten bij de uitvoering van analysemethoden. * Problemen analyseren en oplossen met behulp van gestructureerde methodieken (DMAIC, root cause analysis). * Mede-auteur zijn van documenten voor regelgevende indieningen
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Abgeschlossene Ausbildung als Fachkraft Rohr-, Kanal- und Industrieservice / Umwelttechnologe (m/d/d) für Rohrleitungsnetze und Industrieanlagen * ITS Kanal Services AG * Lohmar * Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - Introduction - Unfortunately, we do not have any translation for this job offer. Please excuse the inconvenience - Die ITS Gruppe und ihre Tochtergesellschaften sind führende Dienstleister, wenn es um den Unterhalt, die Inspektion und die Sanierung von Entwässerungsinfrastruktur, die Reinigung von Strassen und Tunneln sowie die Sanierung von Innenleitungen geht. Wir verfügen nicht nur über ein fundiertes Fachwissen, sondern auch über modernste Ausrüstung für die Instandhaltung von Kanalnetzen, Rohrleitungen, Strassen und Tunneln. Unsere intelligenten und wirtschaftlichen Lösungen werden von priv
Abgeschlossene Ausbildung als Fachkraft Rohr-, Kanal- und Industrieservice / Umwelttechnologe (m/d/d) für Rohrleitungsnetze und Industrieanlagen * ITS Kanal Services AG * Lohmar * Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - Introduction - Unfortunately, we do not have any translation for this job offer. Please excuse the inconvenience - Die ITS Gruppe und ihre Tochtergesellschaften sind führende Dienstleister, wenn es um den Unterhalt, die Inspektion und die Sanierung von Entwässerungsinfrastruktur, die Reinigung von Strassen und Tunneln sowie die Sanierung von Innenleitungen geht. Wir verfügen nicht nur über ein fundiertes Fachwissen, sondern auch über modernste Ausrüstung für die Instandhaltung von Kanalnetzen, Rohrleitungen, Strassen und Tunneln. Unsere intelligenten und wirtschaftlichen Lösungen werden von priv
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Opstellen, uitvoeren en borgen van validatiestudies in samenwerking met Operations, Supply Chain, Technische Dienst en QA * KEY 4 Nova Bv * Achel * Vast contract, onbepaalde tijd * Deeltijds - Solliciteer als één van de eersten - U bent verantwoordelijk voor de validatie van systemen, processen, apparatuur en installaties binnen een hoogtechnologische farmaceutische productie-omgeving. U waarborgt dat alle activiteiten aan de strengste GMP-vereisten voldoen en draagt actief bij aan kwaliteitsverbetering en operationele excellentie. Verantwoordelijkheden * Plannen, uitvoeren en opvolgen van validatie-activiteiten voor systemen, processen en apparatuur * Uitvoeren van interne audits en begeleiden van externe audits (klanten, notified bodies) * Documenteren van validatie-acties en resultaten volgens GMP-procedures * Evalueren van impact bij wijzigingen a
Opstellen, uitvoeren en borgen van validatiestudies in samenwerking met Operations, Supply Chain, Technische Dienst en QA * KEY 4 Nova Bv * Achel * Vast contract, onbepaalde tijd * Deeltijds - Solliciteer als één van de eersten - U bent verantwoordelijk voor de validatie van systemen, processen, apparatuur en installaties binnen een hoogtechnologische farmaceutische productie-omgeving. U waarborgt dat alle activiteiten aan de strengste GMP-vereisten voldoen en draagt actief bij aan kwaliteitsverbetering en operationele excellentie. Verantwoordelijkheden * Plannen, uitvoeren en opvolgen van validatie-activiteiten voor systemen, processen en apparatuur * Uitvoeren van interne audits en begeleiden van externe audits (klanten, notified bodies) * Documenteren van validatie-acties en resultaten volgens GMP-procedures * Evalueren van impact bij wijzigingen a