29 Emplois pour Assurance - Belgique

Ben jij een gedreven ingenieur met een passie voor kwaliteit en verbetering? Wil je jouw expertise inzetten in een dynamische, innovatieve organisatie waar samenwerking en vooruitgang centraal staan? Dan hebben wij dé uitdaging voor jou!

Functieomschrijving
Regio Zwijndrecht zoeken we een Quality Engineer. Jij bent hét aanspreekpunt op kwaliteitsgebied voor een selecte groep van onze belangrijkste klanten. Je zorgt ervoor dat onze kwaliteitsmanagementsystemen altijd up-to-date en in topvorm zijn. Daarbij werk je nauw samen met onze Europese Quality Lead Process Chemicals en speel je een cruciale rol in het verbeteren van processen, producten en systemen.

Verantwoordelijkheden

• Uitvoeren en supporteren van interne en externe audits op producten, processen en systemen.
• Voorstellen en opvolgen van corrigerende / preventieve maatregelen komende uit resultaten van audits, klachten, etc.
• Opvolgen en coördineren van klantenklachten
• Training verzorgen aan medewerkers i.v.m. de zorgsystemen, kwaliteitstechnieken zoals 8D, FMEA, interne auditering.
• Faciliteren van multidisciplinaire processen zoals veranderings-management, business continuity planning, etc.
• Analyseren van bestaande werkmethodieken en faciliteren van verbeteringsplannen.

Profiel

• Master in Chemie, Ingenieurswetenschappen of een vergelijkbare richting.
• Ervaring met kwaliteitsmethodologieën zoals FMEA, 8D, root cause analyse en statistische technieken.
• Sterke communicatieve vaardigheden en een hands-on mentaliteit.
• Oog voor detail en een passie voor continue verbetering.
• If you don't have a valid workpermit, please don't apply!

Arbeidsvoorwaarden

• Contract onbepaalde duur
• Werken in een innovatieve en inspirerende omgeving waar jouw ideeën tellen.
• Samenwerken met een internationaal team en toonaangevende klanten.
• Veel ruimte voor eigen initiatief en professionele ontwikkeling.

Vacature nummer 26234

Let us briefly introduce ourselves!

At Cipal Schaubroeck, we think passion is very important. Passion for your job. Cipal Schaubroeck has therefore been a fixture and the partner of choice for government institutions for more than 30 years. During this period, Cipal Schaubroeck has grown into the largest and most complete provider of digital solutions for the different levels of government in Flanders. We contribute to the overall landscape of the public sector every day. Our strength? That is in our people, who every day with great enthusiasm ensure that our customers are expertly assisted further. Whether it concerns the calculation of their wages, support in their automation or IT processes.

Where will you be based?

As a Test Engineer, you will work closely with our development and analysis team to ensure the quality of our software solutions. You will be involved in every step of the process: from the initial analysis to the automation and execution of tests. Your critical eye and technical expertise help us deliver reliable and efficient solutions for local government departments and public institutions and all of this in an international working environment.

You play an important role in designing testing strategies, building automated tests and analysing complex systems. Thanks to your input, we make sure the applications do exactly what our customers need.

What are we looking for?

We are looking for a Test Engineer with a passion for software quality and a keen analytical mind. You love working together, like to think about how processes can be improved, and are not afraid to share your opinion.

You will need the following skills:

Technical basis: A bachelor's degree in IT or equivalent through experience (min. 3 years in a software or testing environment).

Test automation experience: Knowledge of Cypress or Play, with a foundation in programming (JavaScript/TypeScript).

Analytical & problem-solving: You can help develop and critically review analyses, and have experience writing and optimising test cases.

Communicative & team player: You take responsibility, communicate clearly and stand firmly on your feet. Experience in team leadership is an asset.

Languages: Good command of Dutch and English

What can Cipal Schaubroeck offer you?

Are you looking for an enjoyable working environment where team spirit and innovation are key? Then Cipal Schaubroeck is the ideal place for you!

Attractive remuneration package: Includes an electric car, comprehensive insurance package, meal vouchers, home working allowance and more.

Work-Life Balance: We offer flexible working hours and standard hybrid working, allowing you to maintain a healthy work-life balance.

Training Opportunities: Keep developing with our internal IT Academy and numerous other learning opportunities.

Personal Growth: We believe everyone is the architect of their own career and support your professional ambitions.

Do you want to be part of a leading player in local governmen and work in an international environmentt? Then apply now and discover the many opportunities at Cipal Schaubroeck!

Are you looking for a new opportunity to take your career to a higher orbit? To join an international group with a successful track record in Space Engineering? A job adapted to your career ambitions and in which you could have an impact for the years to come?

We’re seeking a Product Assurance (PA)/Quality Assurance (QA) Engineer with a strong background in software engineering and space product assurance to join our team in Diegem, near Brussels, Belgium.

You will contribute to internal space projects linked to the European Space Agency (ESA), playing a key role in ensuring software and system quality, with direct impact on the success of high-profile missions.

As a member of our team in Belgium, you could be part of a growing, dynamic company that is driving new technologies and services in the space and cybersecurity sectors. Our clients in Belgium include BELSPO, NATO and the European Commission.

Tasks and activities

The scope of work will include:

• Defining and maintaining PA/QA requirements and plans based on ECSS software engineering and product assurance standards.
• Monitoring and controlling the software development lifecycle, ensuring that all quality requirements are fulfilled.
• Guiding project teams in the implementation of QA best practices, ensuring traceability, compliance, and risk control.
• Participating in design, code, documentation, and test reviews, enforcing preventive and corrective actions where necessary.
• Conducting internal quality audits focused on software development, configuration, and release management.
• Participating in progress meetings, project reviews, colocation meetings (ESA) with the review of the QA/PA documentation and Review Item Discrepancy (RIDs) management.
• Supporting the project non-conformance process (NCRs) and attendance/organization of non-conformance/anomaly review boards (NRB) internally as well as with our subcontractors.
• At equipment level, participating in the different reviews, Mandatory Inspection Points with realization of Software PA activities.
• Helping in the process for evaluation and approval of contractors’ requests for waivers (RFW) and deviations (RFD) with respect to baseline.
• Supporting the test preparation and execution, including test data and environment setup, manual and automated testing, oversight of code quality gates and strategy to improve the products.

Skills and experience

The following skills and experience are mandatory:

• Bachelor’s or Master’s Degree in Software Engineering, Computer Science, or a closely Engineering field.
• Minimum of 3 years of experience in software engineering, quality assurance, or software process auditing.
• Excellent interpersonal skills, together with a high degree of organizational and communication abilities, alongside being comfortable working in a diverse and multinational team environment.
• Desire to work both autonomously and as part of a team, in an international multicultural environment.
• Solution oriented mindset, with a customer focused communication skill.
• Fluent in English, both written and spoken.

The following skills and experience would be highly desirable:

• Experience working on ESA projects or in a space/aerospace software environment.
• Background in managing subcontractors’ PA activities.
• Familiarity with Agile methodologies and Scrum frameworks.
• Experience with cloud-native development, containerization, and automated testing.
• Some background in RF systems, signal processing, or ground segment development is a plus.
• Knowledge of ECSS standards:
• ECSS-Q-ST-10 / ECSS-Q-ST-20
• ECSS-E-ST-40C and ECSS-Q-ST-80C
• Hands-on experience with:
• Configuration management in complex systems.
• QA processes in software development environments.
• Tools such as SonarQube, Jira, Bitbucket/GitLab, Docker, and CI/CD platforms (e.g., Jenkins).

Why should you apply?

• You will have the opportunity to work within leading space organisations across Europe.
• We encourage everyone to think outside the box and to push the boundaries of traditional knowledge. This role is an opportunity to join a forward-thinking company and allows for a deeper understanding of the industry.
• To be part of a company that values integrity, inspiration, care and collaboration.
• Benefits include: competitive remuneration packages; unique career opportunities, including working in other countries; access to training and development programmes; flexible relocation support.

We welcome applications from people with disabilities, members of ethnic minorities, all genders, LGBTQ+ individuals and ex-service personnel.

Business Analyst Assurance Vie (H/F)

Bruxelles | CDI / Mission longue durée

À propos d’eXalt

Chez eXalt, nous sommes bien plus qu’un cabinet de conseil : nous sommes une communauté passionnée, engagée dans la transformation digitale des métiers de la finance et de l’assurance. Ici, la collaboration, l’entraide et le partage de connaissances rythment notre quotidien. Nous plaçons l’humain et l’innovation au cœur de notre approche pour accompagner nos clients avec agilité et expertise.

Le défi

Rejoignez un client majeur du secteur assurance pour un projet stratégique. Vous serez le pont entre métiers et équipes digitales.

Votre mission

• Analyser et formaliser les exigences métier liées à la migration
• Collaborer avec équipes métiers, actuariat, opérations et transformation digitale
• Participer aux tests fonctionnels et assurer le reporting

Votre profil

• 5+ ans comme Business Analyst (BPMN, User Stories,.)
• Expérience probante dans le secteur des assurances.
• Expérience en migration de portefeuilles
• Bilingue FR/EN, NL un plus
• Autonome, rigoureux(se) et excellent relationnel

Pourquoi eXalt ?

Une communauté qui valorise l’humain et l’innovation

Des projets à fort impact dans un secteur en pleine évolution

Une structure à taille humaine où vous pouvez vraiment faire la différence

Quality Engineer (QA) - Gent/Remote

Als Quality Engineer binnen een multidisciplinair productteam draag je bij aan het leveren van een hoogwaardig cloudgebaseerd platform dat gericht is op het ondersteunen van kleine en middelgrote ondernemingen bij het beheren van personeelsadministratie en workflows, zoals onboarding, verlofplanning, prestaties en communicatie.

Jouw rol:

• Je ontwikkelt en voert testscenario’s uit om te garanderen dat de software voldoet aan de vereisten en klantverwachtingen.
• Je test webgebaseerde toepassingen, zowel aan de front- als backend, en voert zowel manuele als geautomatiseerde tests uit.
• Focus op Playwright en Javascript.
• Je bewaakt de kwaliteit van het product en let scherp op detail in alle test- en review-momenten.
• Je schrijft en optimaliseert SQL-queries om datakwaliteit en systeemgedrag te analyseren.
• Je voert analyses uit van problemen of nieuwe functionaliteiten en weet zowel technisch als functioneel het overzicht te bewaren.
• Je verdiept je in nieuwe tools, technologieën en domeinkennis, en deelt deze inzichten met het team.
• Je software development collega's ontwikkelen in PHP en Node.js. Leergierigheid om deze talen te leren kennen en verstaan zijn een grote plus!
• Je werkt niet enkel nauw samen met je software development collega’s maar spart ook actief met de support en productmanagement teams.
• Sameb werken jullie in een agile teamstructuur en stel jij verbeteringen voor aan processen en werkwijzen waar mogelijk.

Team & Werkomgeving

• Je komt terecht in een hecht en enthousiast team van getalenteerde collega’s die samenwerken in een open en ondersteunende sfeer.
• De uitvalsbasis is een toffe locatie in hartje Gent, makkelijk bereikbaar en voorzien van alles wat je nodig hebt om comfortabel te werken.
• We combineren kantoorwerk met flexibiliteit: gemiddeld twee dagen per week op kantoor.
• We hanteren typisch een systeem van 38 uur per week.

Iets voor jou?

Voel jij je aangesproken? Solliciteer vandaag nog!

Nexeo est à la recherche de consultants en assurance !

Notre offre

• Vous travaillerez en tant que consultant sur diverses missions et projets non-vie chez nos clients (contrat à durée indéterminée)
• Un salaire intéressant complété par des avantages extralégaux tels qu'une assurance groupe et hospitalisation, un plan de transport à 100 % et la possibilité de disposer d'une voiture de société.
• Vous pouvez également travailler en tant qu'indépendant / freelance
• Nous vous proposons des variations dans votre travail en combinaison avec des possibilités de formation, le moyen idéal de donner une orientation à votre carrière !

Votre profil

• Vous avez au moins un an d'expérience professionnelle pertinente dans la production et la gestion des sinistres BOAR (privé ou d'entreprise) auprès de compagnies d'assurance ou de courtiers d'assurance
• Vous êtes francophone et avez une bonne connaissance du néerlandais
• Vous aimez la variété dans votre travail et vous êtes flexible
• L'enthousiasme, la soif d'apprendre, la passion, l'orientation client, la qualité font partie de votre personnalité.

#Insurance #Verzekeringen #Assurance #BOAR #IARD #Non Life #Life #Consultant

Context

Nuclear medicine has evolved considerably over recent years with the emergence of radiotherapeutics used in the treatment of cancers. The principle is based on the fact that radiotherapeutics can bring radioisotopes to the cancer cells which when they disintegrate, emit radiation that destroys selectively the tumour. Among this therapeutic isotopes, one of the most promising is the alpha-emitting Actinium-225 which is used in the development of new radiotherapeutics by many pharmaceutical companies.

One of the main challenges is to make this radioisotope available in high quality in large quantities. By joining their unique expertise and resources SCK-CEN and IBA have launched the company PanTera which aims at enabling the production of Actinium-225 and make it available for the pharmaceutical industry.

Job Summary

We are seeking an experienced QA Associate specializing in Qualification and Validation to join our quality team. The ideal candidate will have a strong background in quality assurance, a keen eye for detail, and a deep understanding of industry regulations. This role is crucial in ensuring our products meet the highest standards of quality and compliance, thereby maintaining customer satisfaction and regulatory adherence.

The QA Associate (Qualification & Validation) ensures that equipment, systems, processes and facilities comply with regulatory standards and internal quality requirements. This role mainly supports validation activities, documents qualification efforts, and collaborates with cross-functional teams to maintain product quality and regulatory compliance.

The ideal candidate will have a strong background in quality assurance within a manufacturing environment, excellent analytical skills, and the ability to communicate effectively with both internal teams and external suppliers.

Key Responsibilities

Qualification and Validation :

• Support creation and document qualification and validation documents including protocols, master plans, .
• Support validation lifecycle activities, including risk assessments, test plan creation, execution, and summary reporting
• Review and approve validation protocols and reports to ensure completeness and accuracy

Compliance and Documentation :

• Develop and maintain SOPs related to qualification and validation activities
• Assist in audit preparation and participate in internal audits as needed.

Cross-Functional collaboration

• Work closely with engineering, manufacturing, and R&D teams to ensure proper qualification of equipment
• Provide QA oversight for validation activities conducted by third party vendors or contractors
• Train and guide team members on validation processes

Team Support and Backup :

• Act as a backup for other QA team members, providing support during absences or peak workload periods
• Stay familiar with broader QA functions to ensure smooth operations across the Quality department.

Profile

• Bachelor degree in Life Sciences, Chemistry, Engineering, or a related field
• Minimum 5 years of experience in a quality assurance and validation role in the pharmaceutical, industry.
• Strong understanding of validation principles, regulatory requirements, and quality systems.
• Experience with software validation (CSV) is a plus
• Knowledge of risk management tools and methodologies (e.g. FMEA)

Skills and Competencies:

• Excellent organizational skills
• Excellent attention to detail and analytical skills.
• Strong written and verbal communication skills.
• Ability to work independently in a collaborative team environment.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint).
• Quick learner and able to work in a fast-changing environment
• Willingness to work in a controlled environment with adherence to strict safety and regulatory protocols.

Our offer

• Unique opportunity to work in a cutting-edge environment, contributing to the production of critical products used in the fight against cancer
• Collaborative work environment with supportive colleagues who prioritize teamwork
• Thriving start-up company with a dynamic entrepreneurial culture
• Company dedicated to enhancing the quality of life for patients and making a difference in the healthcare industry.

About the Role

Our client, a respected organisation operating in the Belgium, are currently recruiting a Quality Assurance Specialist. The company is committed to delivering high-quality, innovative healthcare solutions and maintaining the highest standards of compliance with regulatory requirements.

This is an excellent opportunity to join a growing, international team and contribute to a strong culture of quality and continuous improvement.

Key Responsibilities

• Support the review and archiving of batch records, logbooks, and basic quality documentation to ensure compliance with internal procedures and regulatory standards.
• Assist in the tracking and documentation of deviations, change controls, and CAPAs within the Quality Management System (QMS).
• Maintain controlled documents, including issuing, updating, and filing SOPs in accordance with document control procedures.
• Participate in internal audits and inspection readiness activities, supporting the QA team in preparing documentation and records for review.
• Collaborate with cross-functional teams, such as Production and Quality Control, to follow up on quality-related actions and support continuous improvement initiatives.

How to apply

If you are interested in this opportunity, please send your CV and a short cover letter highlighting your relevant experience. Applications will be handled in confidence and reviewed on a rolling basis.

ALTEN Belgium est une société de conseil leader dans les domaines de l'ingénierie, des sciences de la vie et de l'informatique dans laquelle les consultants sont au centre.

Pourquoi nous rejoindre ?

Depuis sa création en 2016, la division Life Sciences d’ALTEN Belgium n’a cessé de croitre et occupe aujourd’hui une place de leader sur le marché des Sciences de la Vie et Biotechnologie en Belgique. Rejoindre la division Life Sciences d’ALTEN Belgium et ses 300 consultants, c’est aussi vous offrir la possibilité d’acquérir continuellement de nouvelles expertises pour booster votre carrière. Comment ? En vous permettant de travailler au sein de grandes et petites structures sur les projets les plus stimulants et challengeants du marché !

C’est à travers cette diversité dans nos projets que nous souhaitons vous accompagner dans l’aboutissement de vos objectifs professionnels et vous permettre de performer de manière optimale.

A propos du poste de Coordinateur en Assurance Qualité :

En tant que consultant en Assurance Qualité dans l'industrie pharmaceutique, vous serez amené à travailler dans les départements AQ de nos partenaires en tant que garant de la politique qualité et des objectifs définis conformément aux BPF.

Vos responsabilités seront les suivantes :

• Rédiger les analyses de risques;
• Participer à l'investigation des déviations;
• Effectuer les audits internes;
• Assurer la mise en œuvre correcte et le suivi des CAPA’s;
• Réviser et approuver les documents relatifs aux opérations (SOP’s, outils pédagogiques, lots, rapports et autres documents liés aux BPF);
• Contribuer à l'amélioration du contenu et du processus du système qualité;
• Développer des solutions pour réduire les risques liés à la qualité;
• Assurer l’évaluation des changements dans le cadre de change control.

Votre profil :

• Diplômé d’un Master en Bio-Ingénierie, diplômé en Pharmacie Industrielle ou dans des domaines connexes
• Vous avez une expérience dans les systèmes de qualité (non-conformité, conformité, .) et dans les BPF
• Vous avez connaissance du processus de production et de l'AQ dans l'industrie pharmaceutique
• Vous êtes capable de travailler en anglais en plus du français

Si vous vous reconnaissez dans cette description, alors ce poste est fait pour vous, n’attendez plus pour nous rejoindre !