Jobs in Quality Assurance in Belgium | StepStone

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Uniper: Quality- and Compliance Manager (m/w/d)

Jobs via StepStone.de

Düsseldorf

Therefore, we offer extensive individual compensation packages consisting of a basic salary, a company pension and performance bonuses. At the same time we have flexible working hours including overtime compensation and working from home. Furthermore we are constantly updating many other benefits such as insurance policies, a discounted supply of energy, extra holiday and individual training opportunities. Jobs via StepStone.de * Düsseldorf * Contract duration unspecified * Full Time - Wir sind Uniper, ein internationales Energieunternehmen mit rund 11.000 Mitarbeitern. Wir verfügen über eine ausgewogene Kombination von modernen Großanlagen und ausgezeichneten Technologie- und Marktkenntnissen. Dank unserer Anlagen und Kompetenzen können wir flexibel, präzise und schnell maßgeschneiderte Energieprodukte und -dienstleistungen zu marktfähigen Preisen anbieten. Your responsibilities Therefore, we offer extensive individual compensation packages consisting of a basic salary, a company pension and performance bonuses. At the same time we have flexible working hours including overtime compensation and working from home. Furthermore we are constantly updating many other benefits such as insurance policies, a discounted supply of energy, extra holiday and individual training opportunities. Jobs via StepStone.de * Düsseldorf * Contract duration unspecified * Full Time - Wir sind Uniper, ein internationales Energieunternehmen mit rund 11.000 Mitarbeitern. Wir verfügen über eine ausgewogene Kombination von modernen Großanlagen und ausgezeichneten Technologie- und Marktkenntnissen. Dank unserer Anlagen und Kompetenzen können wir flexibel, präzise und schnell maßgeschneiderte Energieprodukte und -dienstleistungen zu marktfähigen Preisen anbieten. Your responsibilities
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R&D Technician - DYMO

NEWELL BRANDS

Sint-Niklaas

Position title: R&D Technician - DYMO - As a R&D Technician you will be responsible for executing tests and trials. * Sint-Niklaas * Contract duration unspecified * Full Time - Newell Brands (NASDAQ: NWL) is a leading global consumer goods company with a strong portfolio of well-known brands, including Paper Mate®, Sharpie®, Dymo®, EXPO®, Parker®, Elmer's®, Coleman®, Marmot®, Oster®, Sunbeam®, FoodSaver®, Mr. Coffee®, Graco®, Baby Jogger®, NUK®, Calphalon®, Rubbermaid®, Contigo®, First Alert®, and Yankee Candle®. For hundreds of millions of consumers, Newell Brands makes life better every day, where they live, learn, work and play. Location: Sint-Niklaas, BE - Test Lab - Job summary - You will be part of R&D Test Lab department for new DYMO thermal printers and consumables. You will participate in the validation of the design of new products as well as development and qualification of existing products. Position title: R&D Technician - DYMO - As a R&D Technician you will be responsible for executing tests and trials. * Sint-Niklaas * Contract duration unspecified * Full Time - Newell Brands (NASDAQ: NWL) is a leading global consumer goods company with a strong portfolio of well-known brands, including Paper Mate®, Sharpie®, Dymo®, EXPO®, Parker®, Elmer's®, Coleman®, Marmot®, Oster®, Sunbeam®, FoodSaver®, Mr. Coffee®, Graco®, Baby Jogger®, NUK®, Calphalon®, Rubbermaid®, Contigo®, First Alert®, and Yankee Candle®. For hundreds of millions of consumers, Newell Brands makes life better every day, where they live, learn, work and play. Location: Sint-Niklaas, BE - Test Lab - Job summary - You will be part of R&D Test Lab department for new DYMO thermal printers and consumables. You will participate in the validation of the design of new products as well as development and qualification of existing products.
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Support in HPLC Calibration

Brunel Belgium NV

Hulshout

Brunel Belgium NV * Hulshout * Contract duration unspecified * Full Time - About You - Do you want to be part of an international company on the pharmaceutical market? Do you have experience with HPLC? Then maybe this vacancy is your dream job! Your responsibilities * Calibration/requalification of 45 HPLC systems(Waters): need to be able to perform HPLC calibration accordingin-house procedures, need to be able to perform HPLC calibrationaccording stringent project plan, need to be able to document performed calibrationactivities according cGMP requirements * Work according to applicable safety guidelines * Attend daily communications * Work regime: Full time dayshift (8h/day) * 100% site-based work - Your profile * Bachelor's degree in chemistry/sciences/pharmaceutics or equivalent by experience * Knowledge of cGMP requirements * Ability to work precisely and accurately * Good organizational skills * Good communication skills Brunel Belgium NV * Hulshout * Contract duration unspecified * Full Time - About You - Do you want to be part of an international company on the pharmaceutical market? Do you have experience with HPLC? Then maybe this vacancy is your dream job! Your responsibilities * Calibration/requalification of 45 HPLC systems(Waters): need to be able to perform HPLC calibration accordingin-house procedures, need to be able to perform HPLC calibrationaccording stringent project plan, need to be able to document performed calibrationactivities according cGMP requirements * Work according to applicable safety guidelines * Attend daily communications * Work regime: Full time dayshift (8h/day) * 100% site-based work - Your profile * Bachelor's degree in chemistry/sciences/pharmaceutics or equivalent by experience * Knowledge of cGMP requirements * Ability to work precisely and accurately * Good organizational skills * Good communication skills
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QA specialist

Brunel Belgium NV

Antwerpen

At the moment for example, we are looking for a quality assurance specialist to consult one of out clients. Brunel Belgium NV * Antwerpen * Contract duration unspecified * Full Time - About You - Are you someone who likes trying new things and gaining different experiences? Than life as a consultant might be your thing! As a consultancy company specialized in Life Sciences, Infrastructure and IT we are looking for new consultants to . Your responsibilities * Support the cluster quality manager to ensure that the sites under their responsibility comply with Group Quality, food and feed safety policies and standards. * Assist in the management of all relevant documentation associated with certification standards. * Support on quality related topics regarding for instance barley intake, produced malt and blending. At the moment for example, we are looking for a quality assurance specialist to consult one of out clients. Brunel Belgium NV * Antwerpen * Contract duration unspecified * Full Time - About You - Are you someone who likes trying new things and gaining different experiences? Than life as a consultant might be your thing! As a consultancy company specialized in Life Sciences, Infrastructure and IT we are looking for new consultants to . Your responsibilities * Support the cluster quality manager to ensure that the sites under their responsibility comply with Group Quality, food and feed safety policies and standards. * Assist in the management of all relevant documentation associated with certification standards. * Support on quality related topics regarding for instance barley intake, produced malt and blending.
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QA manager

Brunel Belgium NV

Boortmeerbeek

At the moment for example, we are looking for a quality assurance manager to consult one of out clients. * Minimum 5 years of experience in a QA-position, preferably in the Pharmaceutical-related Industry - Brunel Belgium NV * Boortmeerbeek * Contract duration unspecified * Full Time - About You - As a consultancy company specialized in Life Sciences, Infrastructure and IT we are looking for new consultants to . Your responsibilities * Advising on the translation of GDP-, GMP- and customer requirements that need to be integrated in the operational processes. Ensure the incorporation of such requirements in the procedures and instructions and provide training when necessary. * Follow-up of Quality-KPI's. * Review and alignment of Quality Technical Agreements with customers as well as with suppliers. At the moment for example, we are looking for a quality assurance manager to consult one of out clients. * Minimum 5 years of experience in a QA-position, preferably in the Pharmaceutical-related Industry - Brunel Belgium NV * Boortmeerbeek * Contract duration unspecified * Full Time - About You - As a consultancy company specialized in Life Sciences, Infrastructure and IT we are looking for new consultants to . Your responsibilities * Advising on the translation of GDP-, GMP- and customer requirements that need to be integrated in the operational processes. Ensure the incorporation of such requirements in the procedures and instructions and provide training when necessary. * Follow-up of Quality-KPI's. * Review and alignment of Quality Technical Agreements with customers as well as with suppliers.
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Medical Technologist (Microbiology)

PPD

Zaventem

PPD is currently recruiting for a Medical Technologist to join our Central Laboratory in Zaventem, Brussels. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD, we are passionate, deliberate, and driven by our purpose - to improve health! Envision a workplace where you have a direct impact on improving health, , use newest technologies and collaborate with industry thought leaders and therapeutic experts. Welcome to PPD® Laboratories, where science is our passion, quality is our commitment and people are the cornerstone of our success. PPD is currently recruiting for a Medical Technologist to join our Central Laboratory in Zaventem, Brussels. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD, we are passionate, deliberate, and driven by our purpose - to improve health! Envision a workplace where you have a direct impact on improving health, , use newest technologies and collaborate with industry thought leaders and therapeutic experts. Welcome to PPD® Laboratories, where science is our passion, quality is our commitment and people are the cornerstone of our success.
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Deviation Writer

Experis

Walloon Brabant

Our partner is looking for a Deviation Writer to join its team. As Deviation Writer, you will ensure Deviation Management. Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #Deviation #CAPA #Root-Causes #Investigations #Pharma #GMP - You have experience in Deviation management in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? * Management of deviations related to the activity in the building * Define Corrective Actions and Preventive Actions (CAPA) * Initiate and describe deviations in SAP * Investigate to identify root-causes * Propose adequate CAPAs * Follow the management of deviations * Closure of deviations within delay - Your profile - Who are you? Our partner is looking for a Deviation Writer to join its team. As Deviation Writer, you will ensure Deviation Management. Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #Deviation #CAPA #Root-Causes #Investigations #Pharma #GMP - You have experience in Deviation management in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? * Management of deviations related to the activity in the building * Define Corrective Actions and Preventive Actions (CAPA) * Initiate and describe deviations in SAP * Investigate to identify root-causes * Propose adequate CAPAs * Follow the management of deviations * Closure of deviations within delay - Your profile - Who are you?
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Manufactutring Sciences Specialist

Experis

Hainaut

As Manufacturing Sciences Specialist, you are in charge to - Experis * Hainaut * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Uses Six Sigma and DMAIC methods where appropriate. * Defines tasks/experiments to be performed, provides required documentation and ensures also that adequate corrective actions are implemented to address the identified root-cause(s). * Ensures and defends adequate deployment, implementation and utilization of all quality systems as defined by procedures within his organization. Ensures a thorough and timely handling of associated tasks and activities. * Favors communication, critical thinking, problem solving and teamwork across all manufacturing facilities. * Defends investigations in during audits. * Uses QbD, DIDOV, Lean and implements new technologies (including PAT) where appropriate. As Manufacturing Sciences Specialist, you are in charge to - Experis * Hainaut * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Uses Six Sigma and DMAIC methods where appropriate. * Defines tasks/experiments to be performed, provides required documentation and ensures also that adequate corrective actions are implemented to address the identified root-cause(s). * Ensures and defends adequate deployment, implementation and utilization of all quality systems as defined by procedures within his organization. Ensures a thorough and timely handling of associated tasks and activities. * Favors communication, critical thinking, problem solving and teamwork across all manufacturing facilities. * Defends investigations in during audits. * Uses QbD, DIDOV, Lean and implements new technologies (including PAT) where appropriate.
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QA Manager - GMP

Experis

Waals-Brabant

As QA Manager, you are in charge to - Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Ensure the availability, the update and continuous improvement of the quality management system, * Communicate operational issues and opportunities for improvement to department leaders, * Function as Quality department liaison and subject matter expert to other department representatives, customers and regulatory representatives in relation to Supplier qualification, self-inspection, Agency inspections and customer audits, * Contribute to the quality department's activities to ensure continuity of operations, * Know, understand and comply with the company's standard operation procedures and policies, * Perform other related job duties in the context of Quality Assurance as assigned by EU Director, * Perform and and vendors, As QA Manager, you are in charge to - Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Ensure the availability, the update and continuous improvement of the quality management system, * Communicate operational issues and opportunities for improvement to department leaders, * Function as Quality department liaison and subject matter expert to other department representatives, customers and regulatory representatives in relation to Supplier qualification, self-inspection, Agency inspections and customer audits, * Contribute to the quality department's activities to ensure continuity of operations, * Know, understand and comply with the company's standard operation procedures and policies, * Perform other related job duties in the context of Quality Assurance as assigned by EU Director, * Perform and and vendors,
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Project Lead - clinical study

Experis

Charleroi

As Project Leader - clinical study, you are in charge to - Experis * Charleroi * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Management of method validation, assay transfer and sample analysis studies; * Prepares and/or reviews worksheets related to studies; * and training appropriately documented; * Ensures high level documents are signed and acknowledged by personnel involved in the study; * Ensures study binders are up to date; * Follows up on assigned study inventory and sample manifest; * Follows up on deviations ; * Follows up on QC review and ensures it is performed in a timely fashion; * Prepares and/or reviews of data tabulation and study related documents; * ; coordinates with the relevant transversal units (e.g. Data Analysis, QC, Sample Management, QA) to deliver quality data on time; * Submits studies to QA and answers to QA reports; As Project Leader - clinical study, you are in charge to - Experis * Charleroi * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Management of method validation, assay transfer and sample analysis studies; * Prepares and/or reviews worksheets related to studies; * and training appropriately documented; * Ensures high level documents are signed and acknowledged by personnel involved in the study; * Ensures study binders are up to date; * Follows up on assigned study inventory and sample manifest; * Follows up on deviations ; * Follows up on QC review and ensures it is performed in a timely fashion; * Prepares and/or reviews of data tabulation and study related documents; * ; coordinates with the relevant transversal units (e.g. Data Analysis, QC, Sample Management, QA) to deliver quality data on time; * Submits studies to QA and answers to QA reports;
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