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                          17 results for QC Lab Analyst jobs in Brussels within a 30 km radius

                          No match yet? There are 17 more jobs that could match your search

                          QC Specialist

                          Jefferson Wells
                          Braine-l'Alleud, Région wallonne, Belgique
                          Familiarity with the lab and internal techniques.
                          Familiarity with the lab and internal techniques.
                          QC Analyst – Analytical (m/v/x) * Implementeren van nieuwe analytische methoden in de QC-operaties in nauwe samenwerking met Analytical R&D. * Opleiden en ondersteunen van QC-analisten bij de uitvoering van analysemethoden.
                          QC Analyst – Analytical (m/v/x) * Implementeren van nieuwe analytische methoden in de QC-operaties in nauwe samenwerking met Analytical R&D. * Opleiden en ondersteunen van QC-analisten bij de uitvoering van analysemethoden.
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                          BUSINESS DEVELOPMENT MANAGER PHARMA

                          SGS Group Belgium
                          Wavre
                          Easy Apply
                          We're looking for a passionate and driven Business Development Manager to lead the growth of our Pharma QC laboratory services at SGS lab Simon within the Drug Development segment in Europe. You'll build strong relationships, close impactful deals, and help shape the future of SGS lab Simon . * Good understanding of the regulatory QC requirements (GMP, FDA)
                          We're looking for a passionate and driven Business Development Manager to lead the growth of our Pharma QC laboratory services at SGS lab Simon within the Drug Development segment in Europe. You'll build strong relationships, close impactful deals, and help shape the future of SGS lab Simon . * Good understanding of the regulatory QC requirements (GMP, FDA)
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                          Witness approval tests at manufacturer or lab sites in accordance with Vinçotte and EU/UN procedures
                          Witness approval tests at manufacturer or lab sites in accordance with Vinçotte and EU/UN procedures
                          NEW
                          Je bent verantwoordelijk voor het bewaken van alle QC-processen zodat de kwaliteit van het eindproduct en van de toegepaste processen gegarandeerd is om te voldoen aan de verwachtingen en eisen van de klant. * Je staat in voor de validatie van de QC-resultaten opgeleverd door het QC-labo waarbij je product vrijgeeft voor verkoop of blokkeert in de stock. * Je verzorgt rapportering van QC KPI's en vertegenwoordigt het labo in productie ochtendmeetings.
                          Je bent verantwoordelijk voor het bewaken van alle QC-processen zodat de kwaliteit van het eindproduct en van de toegepaste processen gegarandeerd is om te voldoen aan de verwachtingen en eisen van de klant. * Je staat in voor de validatie van de QC-resultaten opgeleverd door het QC-labo waarbij je product vrijgeeft voor verkoop of blokkeert in de stock. * Je verzorgt rapportering van QC KPI's en vertegenwoordigt het labo in productie ochtendmeetings.
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                          NEW
                          Mundo - Lab Nv - Mundo-Lab beheert eco-gerenoveerde en ecologisch beheerde kantoor- en vergaderruimtes die verenigingen, ngo's en sociale ondernemingen die actief zijn op het gebied van duurzame ontwikkeling en maatschappelijke verandering onder één dak samenbrengen. Je rapporteert aan de en in lijn met de waarden van Mundo-Lab ben je verantwoordelijk voor de volgende taken, voor de Mundo Matongé (3600m²), Mundo Trône (3200m²), Mundo Madou (5300m²) in Brussel, Mundo LLN in Louvain-la-Neuve (2000m²), Mundo Namur (3000m²) in Namen en Mundo Antwerpen (2000m²) in Antwerpen. Je deelt dagelijks de waarden van Mundo-Lab (zie )
                          Mundo - Lab Nv - Mundo-Lab beheert eco-gerenoveerde en ecologisch beheerde kantoor- en vergaderruimtes die verenigingen, ngo's en sociale ondernemingen die actief zijn op het gebied van duurzame ontwikkeling en maatschappelijke verandering onder één dak samenbrengen. Je rapporteert aan de en in lijn met de waarden van Mundo-Lab ben je verantwoordelijk voor de volgende taken, voor de Mundo Matongé (3600m²), Mundo Trône (3200m²), Mundo Madou (5300m²) in Brussel, Mundo LLN in Louvain-la-Neuve (2000m²), Mundo Namur (3000m²) in Namen en Mundo Antwerpen (2000m²) in Antwerpen. Je deelt dagelijks de waarden van Mundo-Lab (zie )
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                          De productie van cel- en gentherapieën vraagt daarbij specifieke kennis/ervaring met betrekking tot productieprocessen, de kwaliteitscontroles (QC), materialen en Facility, Utilities, Equipment en Software (FUE S).
                          De productie van cel- en gentherapieën vraagt daarbij specifieke kennis/ervaring met betrekking tot productieprocessen, de kwaliteitscontroles (QC), materialen en Facility, Utilities, Equipment en Software (FUE S).
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                          4 exact matches jobs are outside your preferred location

                          As a Business Analyst, within the 'Lab Data Operations' department, you are in charge of analyzing the risks of data traceability of the testing methods used in the QC department of a global biopharmaceutical company. You work under the supervision of a , and you are in daily contact with many in the QC environment. As Business analyst, you are - in charge to: Understand how data are captured and generated from analytical methods by analyzing the QC department's internal procedures and conducting laboratory observations with ope - You are familiar with the QC environment of pharmaceutical companies.
                          As a Business Analyst, within the 'Lab Data Operations' department, you are in charge of analyzing the risks of data traceability of the testing methods used in the QC department of a global biopharmaceutical company. You work under the supervision of a , and you are in daily contact with many in the QC environment. As Business analyst, you are - in charge to: Understand how data are captured and generated from analytical methods by analyzing the QC department's internal procedures and conducting laboratory observations with ope - You are familiar with the QC environment of pharmaceutical companies.
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                          These jobs might also interest you

                          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
                          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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                          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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                          Support in-licensing activities by providing Quality Assurance expertise for the evaluation of new project opportunities including participation in due diligence activities. * Ensure the Clinical Supply Quality activities are consistent across the range of different environments and teams supported (Vendors / / in house). * Proactively support the activities of Clinical supply for relevant manufacturing quality systems (deviation close out / Change management / complaints / quality improvement). * Identify and facilitate resolution of technical and manufacturing quality issues that may impact the quality of the CMC sections of regulatory submissions. * Management
                          Support in-licensing activities by providing Quality Assurance expertise for the evaluation of new project opportunities including participation in due diligence activities. * Ensure the Clinical Supply Quality activities are consistent across the range of different environments and teams supported (Vendors / / in house). * Proactively support the activities of Clinical supply for relevant manufacturing quality systems (deviation close out / Change management / complaints / quality improvement). * Identify and facilitate resolution of technical and manufacturing quality issues that may impact the quality of the CMC sections of regulatory submissions. * Management
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                          This role for a Dutch speaking QA Lead is crucial to manage Food Safety and Quality during the execution of the Master Plan projects. As an expert in the BC Food Safety standards this role is a key player and the first point of contact in the design, follow up and release for QA of all works that will take place for the Master Plan projects. This expert will lead the site to be fully compliant with BC and industrial Food Safety standards. * Be the first point of contact for QA for all projects related to the Master Plan of Wieze. * Be an expert in the Food Safety standards so that all projects are executed according to the QA expectations. * Strictly follow the QA expectations and QA release of projects and motivate to ensure that QA
                          This role for a Dutch speaking QA Lead is crucial to manage Food Safety and Quality during the execution of the Master Plan projects. As an expert in the BC Food Safety standards this role is a key player and the first point of contact in the design, follow up and release for QA of all works that will take place for the Master Plan projects. This expert will lead the site to be fully compliant with BC and industrial Food Safety standards. * Be the first point of contact for QA for all projects related to the Master Plan of Wieze. * Be an expert in the Food Safety standards so that all projects are executed according to the QA expectations. * Strictly follow the QA expectations and QA release of projects and motivate to ensure that QA
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                          What is the average salary for QC Lab Analyst in Brussels?

                          Average salary per year
                          39.400 €

                          The average salary for a QC Lab Analyst in Brussels is 39.400 €. QC Lab Analyst in Brussels salaries range from 33.200 € to 48.900 €.

                          Frequently Asked Questions

                          How many QC Lab Analyst jobs are there in Brussels?
                          There are 17 QC Lab Analyst jobs within 20 miles of Brussels available on StepStone right now.

                          What other similar jobs are there to QC Lab Analyst jobs in Brussels?
                          As well as QC Lab Analyst jobs in Brussels, you can find Engineering, Manufacturing, Analysis, amongst many others.

                          Which skills are beneficial for QC Lab Analyst jobs in Brussels?
                          The following skills are useful for QC Lab Analyst jobs in Brussels: Manufacturing, Analysis, Quality Control, Communication, Engineering.

                          Which industry do QC Lab Analyst jobs in Brussels belong to?
                          QC Lab Analyst jobs in Brussels are part of the Science industry.