4 Emplois pour Qa Engineer - Belgique
Experienced QA/test engineer
Leuven, Vlaams Brabant
Phished
Publié il y a 22 jours
Emploi consulté
Description De L'emploi
Testing PHP Cybersecurity
In just five years, we’ve grown from an ambitious start-up to the fastest-growing Cybersecurity Awareness Platform in the world. Today, we protect over 1.5 million users across 5,000 organizations, together with 300+ partners worldwide.
From 5 employees to an international team of more than 70 driven colleagues – and we’re still growing.
Phished is a rapidly growing tech scale-up that helps organizations improve their cybersecurity. Through a unique, fully automated training platform , employees are trained to recognize real cyberattacks and respond to them in the correct way. In doing so, we make a real impact on both individuals and organizations.
Does this sound like you? Read on.
Your responsibilities
You will review feature passports, technical documentation and issues requirements to provide timely and meaningful feedback.
You create and execute on detailed, comprehensive and well-structured test plans and test cases.
You are involved in the design, implementation and execution of automated tests using tools in the PHP ecosystem (automatic)
You identify, record, document and track bugs and you set up and monitor quality assurance metrics
You are an integral part of the development team and you support the team to implement automated tests.
You write documentation related to the testing processes to facilitate knowledge sharing and transparency.
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0
Quality Assurance Engineer
Zaventem, Vlaams Brabant
Hologic
Publié il y a 13 jours
Emploi consulté
Description De L'emploi
Quality Assurance Engineer
Zaventem, Vlaams Brabant, Belgium
**Quality Assurance Engineer, Distribution (EMEA)**
**Role location** : Zaventem, Belgium
**Travel:** 10-15%
At Hologic, we are driven by our purpose to enable healthier lives everywhere, every day. As a leader in medical technology, we are dedicated to improving health outcomes through innovation, integrity and uncompromising quality.
We are now looking for an experienced Quality Assurance Engineer to join our team in Zaventem, Belgium. As Quality Assurance Engineer specializing in distribution, you will play a vital role in upholding product integrity across the supply chain. You will be responsible for managing distributor relationships, implementing robust quality assurance measures and ensuring full compliance with regulatory requirements, quality standards and Good Distribution Practices (GDP).
**Role Responsibilities:**
+ Distributor Management: evaluate and oversee new and existing distributors to ensure they meet both regulatory and organizational requirements
+ Quality Compliance: ensure audits, validations, and other quality activities are completed to maintain the effectiveness of Hologic's Quality System
+ Cross-Functional Collaboration: work closely with Regulatory Affairs and other departments to identify local distribution requirements and ensure compliance regarding product storage, handling, transportation, traceability and reporting
+ Documentation & Reporting: maintain comprehensive records of distributor compliance, including assessments, quality agreements, audits, and corrective actions
+ Risk & Non-Conformance Management: investigate non-conformances and implement corrective and preventive actions to eliminate re-occurrence
+ Stakeholder Engagement: serve as the primary contact for distributor quality-related inquiries, providing expert guidance and regular updates
+ Continuous Improvement: develop and track metrics and KPIs to monitor distributor quality performance and support ongoing improvement initiatives
+ SOP Development: participate in the creation and maintenance of SOPs related to distribution activities
+ Audit Support: provide QA expertise during internal and external audits
**Knowledge, skills and experience:**
+ Background in Engineering, Quality Assurance, Supply Chain Management, Logistics or a related field
+ Experience in medical device manufacturing or a related industry, ideally in a quality-focused role
+ Knowledge of Good Distribution Practices (GDP), ISO 9001/13485, EU MDR/IVDR and medical device regulations
+ Proven experience in root cause analysis, risk assessment, CAPA and audit processes
+ Experience with logistics and distribution processes will be advantageous
+ Excellent communication, negotiation and interpersonal skills-able to engage effectively with both internal and external stakeholders
+ Analytical and problem-solving mindset with a proactive and organized approach to managing multiple priorities
+ Adaptability to change and the ability to work both independently and as part of a collaborative team
If you're excited by the opportunity to leverage your quality assurance expertise in a fast-paced, mission-driven company, we want to hear from you. Apply today and join us at Hologic!
#LI-KP1
#associate
Zaventem, Vlaams Brabant, Belgium
**Quality Assurance Engineer, Distribution (EMEA)**
**Role location** : Zaventem, Belgium
**Travel:** 10-15%
At Hologic, we are driven by our purpose to enable healthier lives everywhere, every day. As a leader in medical technology, we are dedicated to improving health outcomes through innovation, integrity and uncompromising quality.
We are now looking for an experienced Quality Assurance Engineer to join our team in Zaventem, Belgium. As Quality Assurance Engineer specializing in distribution, you will play a vital role in upholding product integrity across the supply chain. You will be responsible for managing distributor relationships, implementing robust quality assurance measures and ensuring full compliance with regulatory requirements, quality standards and Good Distribution Practices (GDP).
**Role Responsibilities:**
+ Distributor Management: evaluate and oversee new and existing distributors to ensure they meet both regulatory and organizational requirements
+ Quality Compliance: ensure audits, validations, and other quality activities are completed to maintain the effectiveness of Hologic's Quality System
+ Cross-Functional Collaboration: work closely with Regulatory Affairs and other departments to identify local distribution requirements and ensure compliance regarding product storage, handling, transportation, traceability and reporting
+ Documentation & Reporting: maintain comprehensive records of distributor compliance, including assessments, quality agreements, audits, and corrective actions
+ Risk & Non-Conformance Management: investigate non-conformances and implement corrective and preventive actions to eliminate re-occurrence
+ Stakeholder Engagement: serve as the primary contact for distributor quality-related inquiries, providing expert guidance and regular updates
+ Continuous Improvement: develop and track metrics and KPIs to monitor distributor quality performance and support ongoing improvement initiatives
+ SOP Development: participate in the creation and maintenance of SOPs related to distribution activities
+ Audit Support: provide QA expertise during internal and external audits
**Knowledge, skills and experience:**
+ Background in Engineering, Quality Assurance, Supply Chain Management, Logistics or a related field
+ Experience in medical device manufacturing or a related industry, ideally in a quality-focused role
+ Knowledge of Good Distribution Practices (GDP), ISO 9001/13485, EU MDR/IVDR and medical device regulations
+ Proven experience in root cause analysis, risk assessment, CAPA and audit processes
+ Experience with logistics and distribution processes will be advantageous
+ Excellent communication, negotiation and interpersonal skills-able to engage effectively with both internal and external stakeholders
+ Analytical and problem-solving mindset with a proactive and organized approach to managing multiple priorities
+ Adaptability to change and the ability to work both independently and as part of a collaborative team
If you're excited by the opportunity to leverage your quality assurance expertise in a fast-paced, mission-driven company, we want to hear from you. Apply today and join us at Hologic!
#LI-KP1
#associate
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1
Quality Assurance Lab Associate
Beerse, Antwerpen
J&J Family of Companies
Hier
Emploi consulté
Description De L'emploi
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at Function:**
Quality
**Job Sub** **Function:**
Quality Assurance
**Job Category:**
Professional
**All Job Posting Locations:**
Beerse, Antwerp, Belgium
**Job Description:**
**About Innovative Medicine**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at are searching for the best talent for QA lab associate QC to be based in Beerse !**
This role focuses on ensuring laboratory compliance, with accurate and timely review of investigations and careful analysis of QC data to identify trends that can drive quality improvements. You'll be part of a collaborative quality team that partners across functions to strengthen regulatory readiness and continuous improvement. This is a role that values initiative, learning, and contributing to a culture of safety and quality!
**As a QA lab associate QC you will:**
**·** Provide compliance oversight for the laboratories, ensuring accurate and timely review of laboratory investigations, performing analysis on quality indicating data and identifying any trends noted for QC data.
**·** Support drafting and approving of standard operating procedures.
**·** Perform spot-checks in the Lab to ensure compliance with written regulations, policies, procedures, and global procedures.
**·** Ensure non-conformances are investigated thoroughly and approved in a timely manner and appropriate corrective and preventive action plans are implemented.
**·** Strive to reduce non-conformances in supported areas by proactively driving compliance.
**·** Provide compliance oversight for analytical instrument qualification.
**Qualifications/Requirements:**
**·** A minimum of a Master Degree in Engineering, Science or equivalent technical discipline.
**·** A minimum of 2 years of experience in Quality Assurance.
**·** Knowledge of cGMP regulations.
**·** Knowledge of FDA/EU guidance.
**·** Experience in methods like flow cytometry , PCR , Elisa , Endotoxine testing
**·** Experience with cell counting and viability.
At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.
**Here's what you can expect:**
**·** **Application review:** We'll carefully review your CV to see how your skills and experience align with the role.
**· Getting to know you:** If there's a good match, you'll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
**· Staying informed:** We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
**· Final steps:** For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.
Finally, at the end of the process, we'll invite you to share feedback in a short survey - your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We're excited to learn more about you and wish you the best of luck in the process! #RPOEMEA #LI_Hybrid
Quality
**Job Sub** **Function:**
Quality Assurance
**Job Category:**
Professional
**All Job Posting Locations:**
Beerse, Antwerp, Belgium
**Job Description:**
**About Innovative Medicine**
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at are searching for the best talent for QA lab associate QC to be based in Beerse !**
This role focuses on ensuring laboratory compliance, with accurate and timely review of investigations and careful analysis of QC data to identify trends that can drive quality improvements. You'll be part of a collaborative quality team that partners across functions to strengthen regulatory readiness and continuous improvement. This is a role that values initiative, learning, and contributing to a culture of safety and quality!
**As a QA lab associate QC you will:**
**·** Provide compliance oversight for the laboratories, ensuring accurate and timely review of laboratory investigations, performing analysis on quality indicating data and identifying any trends noted for QC data.
**·** Support drafting and approving of standard operating procedures.
**·** Perform spot-checks in the Lab to ensure compliance with written regulations, policies, procedures, and global procedures.
**·** Ensure non-conformances are investigated thoroughly and approved in a timely manner and appropriate corrective and preventive action plans are implemented.
**·** Strive to reduce non-conformances in supported areas by proactively driving compliance.
**·** Provide compliance oversight for analytical instrument qualification.
**Qualifications/Requirements:**
**·** A minimum of a Master Degree in Engineering, Science or equivalent technical discipline.
**·** A minimum of 2 years of experience in Quality Assurance.
**·** Knowledge of cGMP regulations.
**·** Knowledge of FDA/EU guidance.
**·** Experience in methods like flow cytometry , PCR , Elisa , Endotoxine testing
**·** Experience with cell counting and viability.
At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.
**Here's what you can expect:**
**·** **Application review:** We'll carefully review your CV to see how your skills and experience align with the role.
**· Getting to know you:** If there's a good match, you'll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
**· Staying informed:** We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
**· Final steps:** For successful candidates, you will need to complete country-specific checks before starting your new role. We will help guide you through these.
Finally, at the end of the process, we'll invite you to share feedback in a short survey - your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. We're excited to learn more about you and wish you the best of luck in the process! #RPOEMEA #LI_Hybrid
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Désolé, cet emploi n'est pas disponible dans votre région
2
Responsable de la Conformité Pharmaceutique (Quality Assurance)
3500 Hasselt, Limburg
WhatJobs
Publié il y a 17 jours
Emploi consulté
Description De L'emploi
Notre client, une entreprise pharmaceutique reconnue pour son excellence en recherche et développement, recrute un Responsable de la Conformité Pharmaceutique (Assurance Qualité) pour renforcer son équipe globale. Ce poste stratégique est entièrement à distance, vous permettant de travailler depuis votre bureau.
Vous serez responsable de la supervision et de la mise en œuvre des systèmes d'assurance qualité (AQ) et de conformité réglementaire pour garantir que tous les produits et processus respectent les normes nationales et internationales (par exemple, GMP, GCP, GLP). Vous jouerez un rôle clé dans la préparation des inspections réglementaires et des audits clients, en assurant la documentation appropriée et la réponse aux non-conformités.
Vos missions incluront le développement, la révision et l'approbation des procédures opératoires standardisées (POS), des protocoles d'études, des rapports et de toute la documentation liée à la qualité. Vous dirigerez des investigations sur les déviations, les réclamations produits et les plans d'actions correctives et préventives (CAPA). La formation du personnel sur les bonnes pratiques de fabrication et les exigences réglementaires fera également partie de vos responsabilités.
Vous travaillerez en étroite collaboration avec les départements de production, de recherche et développement, de contrôle qualité et les affaires réglementaires pour assurer une approche intégrée de la qualité. Vous conseillerez la direction sur les aspects de conformité et les risques potentiels, et contribuerez à l'amélioration continue des processus qualité.
Le candidat idéal possède un diplôme supérieur (pharmacien, biologiste, ingénieur) et une solide expérience (minimum 8 ans) dans le domaine de l'assurance qualité et de la conformité réglementaire dans l'industrie pharmaceutique ou biotechnologique. Une connaissance approfondie des réglementations applicables (EMA, FDA) et des systèmes de gestion de la qualité est indispensable. D'excellentes compétences en communication, en analyse, en résolution de problèmes et en leadership sont requises. La capacité à gérer plusieurs projets simultanément, à travailler de manière autonome et à influencer positivement les équipes est essentielle. La maîtrise de l'anglais est obligatoire.
Ce rôle est exclusivement à distance.
Vous serez responsable de la supervision et de la mise en œuvre des systèmes d'assurance qualité (AQ) et de conformité réglementaire pour garantir que tous les produits et processus respectent les normes nationales et internationales (par exemple, GMP, GCP, GLP). Vous jouerez un rôle clé dans la préparation des inspections réglementaires et des audits clients, en assurant la documentation appropriée et la réponse aux non-conformités.
Vos missions incluront le développement, la révision et l'approbation des procédures opératoires standardisées (POS), des protocoles d'études, des rapports et de toute la documentation liée à la qualité. Vous dirigerez des investigations sur les déviations, les réclamations produits et les plans d'actions correctives et préventives (CAPA). La formation du personnel sur les bonnes pratiques de fabrication et les exigences réglementaires fera également partie de vos responsabilités.
Vous travaillerez en étroite collaboration avec les départements de production, de recherche et développement, de contrôle qualité et les affaires réglementaires pour assurer une approche intégrée de la qualité. Vous conseillerez la direction sur les aspects de conformité et les risques potentiels, et contribuerez à l'amélioration continue des processus qualité.
Le candidat idéal possède un diplôme supérieur (pharmacien, biologiste, ingénieur) et une solide expérience (minimum 8 ans) dans le domaine de l'assurance qualité et de la conformité réglementaire dans l'industrie pharmaceutique ou biotechnologique. Une connaissance approfondie des réglementations applicables (EMA, FDA) et des systèmes de gestion de la qualité est indispensable. D'excellentes compétences en communication, en analyse, en résolution de problèmes et en leadership sont requises. La capacité à gérer plusieurs projets simultanément, à travailler de manière autonome et à influencer positivement les équipes est essentielle. La maîtrise de l'anglais est obligatoire.
Ce rôle est exclusivement à distance.
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