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                          23 results for Assistant Quality Management jobs in Gosselies within a 30 km radius

                          Product Quality Specialist

                          HAYS
                          Braine-l'Alleud
                          To strengthen its Supply Chain team, we are looking for a Product Quality Specialist. * Professional Experience: Experience in product quality management and in the industry. Our client is an international company active worldwide, specializing in the management and distribution of petroleum and chemical products. * Manage product quality, analyze and determine blending plans. * Support the in investigating product quality complaints, product non-compliance, and client audit planning.
                          To strengthen its Supply Chain team, we are looking for a Product Quality Specialist. * Professional Experience: Experience in product quality management and in the industry. Our client is an international company active worldwide, specializing in the management and distribution of petroleum and chemical products. * Manage product quality, analyze and determine blending plans. * Support the in investigating product quality complaints, product non-compliance, and client audit planning.
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                          No match yet? There are 22 more jobs that could match your search

                          Vendor Quality Lead

                          Jefferson Wells
                          Braine-l'Alleud, Région wallonne, Belgique
                          Solid experience in Quality Agreements lifecycle management. We are looking for a Vendor Quality Lead to reinforce the R&D & Pharmacovigilance Vendor Quality team. The role is needed to support GCP-focused vendor qualification activities, quality agreements setup, and vendor oversight, especially due to a current backlog of agreements and increasing number of GCP vendors. * Handling the setup, review, update and closure of Quality Agreements (priority scope). * Strong GCP background + clinical trial management understanding. * Proven experience in vendor qualification / vendor management. * Legal/paralegal background is an asset for Quality Agreement work. * Vendor management experience in additional GxP areas (but not GMP/GDP profiles).
                          Solid experience in Quality Agreements lifecycle management. We are looking for a Vendor Quality Lead to reinforce the R&D & Pharmacovigilance Vendor Quality team. The role is needed to support GCP-focused vendor qualification activities, quality agreements setup, and vendor oversight, especially due to a current backlog of agreements and increasing number of GCP vendors. * Handling the setup, review, update and closure of Quality Agreements (priority scope). * Strong GCP background + clinical trial management understanding. * Proven experience in vendor qualification / vendor management. * Legal/paralegal background is an asset for Quality Agreement work. * Vendor management experience in additional GxP areas (but not GMP/GDP profiles).
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                          En tant que Quality Manager, vous êtes le garant de la conformité réglementaire et le moteur de la performance opérationnelle sur le terrain. Vous assurez le respect strict du Programme National de Sûreté de l'Aviation Civile (PNS) et gérez le système de management de la qualité (ISO 9001).
                          En tant que Quality Manager, vous êtes le garant de la conformité réglementaire et le moteur de la performance opérationnelle sur le terrain. Vous assurez le respect strict du Programme National de Sûreté de l'Aviation Civile (PNS) et gérez le système de management de la qualité (ISO 9001).
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                          Our partner is looking for a R&D and Pharmacovigilance Digital Quality lead to join its team. * Oversee the validation and lifecycle control of external computerized systems used by CROs or third-party service providers, ensuring they meet internal quality and regulatory expectations. * Work with Computer System QA team and Clinical Operations to ensure that DI controls (including ALCOA+ principles, metadata management, audit trails, system-to-system data transfer checks, and dataflow mapping) are embedded across the full data lifecycle. * Strong communication skills, able to convey quality concepts and DI/CSV requirements to diverse technical and non-technical stakeholders.
                          Our partner is looking for a R&D and Pharmacovigilance Digital Quality lead to join its team. * Oversee the validation and lifecycle control of external computerized systems used by CROs or third-party service providers, ensuring they meet internal quality and regulatory expectations. * Work with Computer System QA team and Clinical Operations to ensure that DI controls (including ALCOA+ principles, metadata management, audit trails, system-to-system data transfer checks, and dataflow mapping) are embedded across the full data lifecycle. * Strong communication skills, able to convey quality concepts and DI/CSV requirements to diverse technical and non-technical stakeholders.
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                          Solide expérience en people management. Si vous souhaitez rejoindre un environnement exigeant où votre expertise logistique et vos compétences en management feront la différence, nous attendons votre candidature.
                          Solide expérience en people management. Si vous souhaitez rejoindre un environnement exigeant où votre expertise logistique et vos compétences en management feront la différence, nous attendons votre candidature.
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                          Enter and Manage Deviations and CAPA as per Source Quality (Veeva System) Deviation management processes. * Experience with managing non-compliance issues in Quality Management system as per deviation management processes. * Identify quality issues that would classify as deviation events and facilitate the deviation investigation and root-cause analysis. * Assess proposed CAPA of vendors and liaise with , (Quality or business) to ensure robust CAPAs are developed and negotiate the major observations with vendors or the company business partners. * Manage, track and facilitate the project management of timely review, evidence evaluation and closure of deviations and CAPA's from deviations, audits and inspections. Monitor the performance of (quality) systems and solutions and the quality of data to support oversight on critical to quality indicators and key decisions.
                          Enter and Manage Deviations and CAPA as per Source Quality (Veeva System) Deviation management processes. * Experience with managing non-compliance issues in Quality Management system as per deviation management processes. * Identify quality issues that would classify as deviation events and facilitate the deviation investigation and root-cause analysis. * Assess proposed CAPA of vendors and liaise with , (Quality or business) to ensure robust CAPAs are developed and negotiate the major observations with vendors or the company business partners. * Manage, track and facilitate the project management of timely review, evidence evaluation and closure of deviations and CAPA's from deviations, audits and inspections. Monitor the performance of (quality) systems and solutions and the quality of data to support oversight on critical to quality indicators and key decisions.
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                          People Management : Coacher, développer et motiver votre équipe d'inspecteurs afin d'optimiser l'utilisation et le développement de leurs compétences, savoir-faire et connaissances, tout en garantissant un suivi rapide, sûr et efficace des activités. * Technical Management : Vous restez à jour sur toutes les nouvelles évolutions dans votre domaine d'expertise technique, vous formez continuellement et conseillez clients et collègues. o Vous disposez de solides compétences en management et leadership.
                          People Management : Coacher, développer et motiver votre équipe d'inspecteurs afin d'optimiser l'utilisation et le développement de leurs compétences, savoir-faire et connaissances, tout en garantissant un suivi rapide, sûr et efficace des activités. * Technical Management : Vous restez à jour sur toutes les nouvelles évolutions dans votre domaine d'expertise technique, vous formez continuellement et conseillez clients et collègues. o Vous disposez de solides compétences en management et leadership.
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                          People Management : Coacher, développer et motiver votre équipe d'inspecteurs afin d'optimiser l'utilisation et le développement de leurs compétences, savoir-faire et connaissances, tout en garantissant un suivi rapide, sûr et efficace des activités. * Technical Management Vous restez à jour sur toutes les nouvelles évolutions dans votre domaine d'expertise technique, vous formez continuellement et conseillez clients et collègues. o Vous disposez de solides compétences en management et leadership.
                          People Management : Coacher, développer et motiver votre équipe d'inspecteurs afin d'optimiser l'utilisation et le développement de leurs compétences, savoir-faire et connaissances, tout en garantissant un suivi rapide, sûr et efficace des activités. * Technical Management Vous restez à jour sur toutes les nouvelles évolutions dans votre domaine d'expertise technique, vous formez continuellement et conseillez clients et collègues. o Vous disposez de solides compétences en management et leadership.
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                          Ensure fit for purpose of Digital Operations solutions, and solution & business readiness for implementation – further support change management by monitoring the adoption and performance of newly implemented solutions * Hand-on experience and strong understanding of CMC Development laboratory workflows (small molecules, biologics, analytical development, sample & inventory management) * Knowledge of regulatory requirements and quality standards in the biopharmaceutical industry is a plus
                          Ensure fit for purpose of Digital Operations solutions, and solution & business readiness for implementation – further support change management by monitoring the adoption and performance of newly implemented solutions * Hand-on experience and strong understanding of CMC Development laboratory workflows (small molecules, biologics, analytical development, sample & inventory management) * Knowledge of regulatory requirements and quality standards in the biopharmaceutical industry is a plus
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                          In practice the QA Scheduler will support determining activities lead times, ability of the various Quality departments to abide by supply scheduling according to those defined lead times, review progress against schedule following on potential issues and delays, enabling prioritization and enhancing capacity planning. * Prepare QA and adjacent teams for adoption through training, role clarity, and change management * Previous experience in change management would be an advantage
                          In practice the QA Scheduler will support determining activities lead times, ability of the various Quality departments to abide by supply scheduling according to those defined lead times, review progress against schedule following on potential issues and delays, enabling prioritization and enhancing capacity planning. * Prepare QA and adjacent teams for adoption through training, role clarity, and change management * Previous experience in change management would be an advantage
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                          BUSINESS DEVELOPMENT MANAGER, PHARMA, BIOANALYSIS DIVISION

                          SGS Group Belgium
                          Wavre
                          Easy Apply
                          We're also the benchmark worldwide for quality and integrity. * Scientific educational or Business Management education
                          We're also the benchmark worldwide for quality and integrity. * Scientific educational or Business Management education
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                          Safety, health and quality supremacy as a foundation * Ensure data quality, consistency, and timely reporting * Strong analytical and data management skills * Very good communication and stakeholder management skills
                          Safety, health and quality supremacy as a foundation * Ensure data quality, consistency, and timely reporting * Strong analytical and data management skills * Very good communication and stakeholder management skills
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                          En forte croissance, nous nous appuyons sur nos talents et nos valeurs pour poursuivre notre expansion en Belgique, en France et au Luxembourg dans nos métiers techniques, dans le Facility Management et le secteur des titres-services.
                          En forte croissance, nous nous appuyons sur nos talents et nos valeurs pour poursuivre notre expansion en Belgique, en France et au Luxembourg dans nos métiers techniques, dans le Facility Management et le secteur des titres-services.
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                          Easy Apply
                          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. * People management (support, evaluation, hiring)
                          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. * People management (support, evaluation, hiring)
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                          24 exact matches jobs are outside your preferred location

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                          What is the average salary for Assistant Quality Management in Gosselies?

                          Average salary per year
                          46.000 €

                          The average salary for a Assistant Quality Management in Gosselies is 46.000 €. Assistant Quality Management in Gosselies salaries range from 38.700 € to 55.600 €.

                          Frequently Asked Questions

                          How many Assistant Quality Management jobs are there in Gosselies?
                          There are 23 Assistant Quality Management jobs within 20 miles of Gosselies available on StepStone right now.

                          What other similar jobs are there to Assistant Quality Management jobs in Gosselies?
                          As well as Assistant Quality Management jobs in Gosselies, you can find Management, Communication, Business, amongst many others.

                          Which skills are beneficial for Assistant Quality Management jobs in Gosselies?
                          The following skills are useful for Assistant Quality Management jobs in Gosselies: Communication, Management, Business, Sales, Development.

                          Which industry do Assistant Quality Management jobs in Gosselies belong to?
                          Assistant Quality Management jobs in Gosselies are part of the Manufacturing industry.

                          How many temporary and part-time Assistant Quality Management jobs are available in Gosselies?
                          There are 0 temporary Assistant Quality Management jobs and 1 part-time Assistant Quality Management jobs available in Gosselies at the moment.