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                        4 resultaten voor Cro in Waver binnen een straal van 30 km

                        BUSINESS DEVELOPMENT MANAGER, PHARMA, BIOANALYSIS DIVISION

                        SGS Group Belgium
                        Wavre
                        Snel solliciteren
                        SGS Group Belgium * Wavre * Vast contract, onbepaalde tijd * Voltijds - Snel solliciteren - Company Description - SGS is the world's leading inspection, verification, testing and certification company. We're also the benchmark worldwide for quality and integrity. And that makes us very proud. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise. Job Description - As Business Development Manager you will be responsible for identifying and exploring strategic business development opportunities within the Bioanalysis division to maximize organization growth. * Actively prospecting new customers and new business opportunities worldwide and develop new opportunities with existing clients on Preclinical (GLP) and Clinical (GCLP) Bioanalytical projects. with your ...
                        SGS Group Belgium * Wavre * Vast contract, onbepaalde tijd * Voltijds - Snel solliciteren - Company Description - SGS is the world's leading inspection, verification, testing and certification company. We're also the benchmark worldwide for quality and integrity. And that makes us very proud. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise. Job Description - As Business Development Manager you will be responsible for identifying and exploring strategic business development opportunities within the Bioanalysis division to maximize organization growth. * Actively prospecting new customers and new business opportunities worldwide and develop new opportunities with existing clients on Preclinical (GLP) and Clinical (GCLP) Bioanalytical projects. with your ...
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                        R&D and Pharmacovigilance Digital Quality lead

                        Jefferson Wells
                        Braine-l'Alleud
                        Jefferson Wells * Braine-l'Alleud * Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - Brabant Wallon – Contracting - Our partner is looking for a R&D and Pharmacovigilance Digital Quality lead to join its team. This international company is well known for its pharmaceuticals. Your responsibilities - GxP System & Technology Compliance * Ensure GLP, GCP, GVP and GRA business systems are fully compliant with regulatory expectations (e.g. OECD, ICH, GVP) and internal digital governance requirements. * Maintain and evolve the compliance framework for GxP-relevant systems (policies, SOPs, guidance). * Provide QA insight during system selection, onboarding, validation, and ongoing oversight. * Support investigations, deviations, CAPAs, and inspection-readiness activities related to DI or system failures, ensuring completeness and alignment with regulatory ...
                        Jefferson Wells * Braine-l'Alleud * Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - Brabant Wallon – Contracting - Our partner is looking for a R&D and Pharmacovigilance Digital Quality lead to join its team. This international company is well known for its pharmaceuticals. Your responsibilities - GxP System & Technology Compliance * Ensure GLP, GCP, GVP and GRA business systems are fully compliant with regulatory expectations (e.g. OECD, ICH, GVP) and internal digital governance requirements. * Maintain and evolve the compliance framework for GxP-relevant systems (policies, SOPs, guidance). * Provide QA insight during system selection, onboarding, validation, and ongoing oversight. * Support investigations, deviations, CAPAs, and inspection-readiness activities related to DI or system failures, ensuring completeness and alignment with regulatory ...
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                        Psi Cro Belgium BV * Leuven - Solliciteer als één van de eersten - Introduction - PSI is a leading Contract Research Organization with over 30 years on the market, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Your tasks - Job Description - As a Clinical Trial Liaison, you will help clinical sites identify and recruit patients more efficiently by providing protocol‑focused support. Acting as the face of PSI on-site, you will be a key contributor to the success of our clinical trials and a trusted resource for site teams. * Serve as a specialized liaison to support sites with a protocol‑tailored strategy that enhances patient identification and recruitment efficiency. * Guide clinical sites in developing and implementing effective patient enrolment ...
                        Psi Cro Belgium BV * Leuven - Solliciteer als één van de eersten - Introduction - PSI is a leading Contract Research Organization with over 30 years on the market, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Your tasks - Job Description - As a Clinical Trial Liaison, you will help clinical sites identify and recruit patients more efficiently by providing protocol‑focused support. Acting as the face of PSI on-site, you will be a key contributor to the success of our clinical trials and a trusted resource for site teams. * Serve as a specialized liaison to support sites with a protocol‑tailored strategy that enhances patient identification and recruitment efficiency. * Guide clinical sites in developing and implementing effective patient enrolment ...
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                        NIEUW
                        Psi Cro Belgium BV * Leuven - Solliciteer als één van de eersten - Introduction - PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Your tasks - Job Description - PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-being. Hybrid working based in LeuvenBelgium * Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Advise clients, , sites, regulatory agencies and third-party vendors on medical matters
                        Psi Cro Belgium BV * Leuven - Solliciteer als één van de eersten - Introduction - PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Your tasks - Job Description - PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-being. Hybrid working based in LeuvenBelgium * Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Advise clients, , sites, regulatory agencies and third-party vendors on medical matters
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                        The Medical Review Manager (Temporary assignment) will be a key member of the Medical Information and Review (MI&R) Group. As a key partner to in-country Medical Affairs and Marketing colleagues, this position aims to minimize compliance risks by ensuring review and approval of promotional and non-promotional marketing materials, as well as Medical to Medical content ensuring alignment with all applicable country laws, regulations, and industry codes. * Act as the point of contact for Medical Review, enabling efficient review processes for both promotional/ non-promotional and Medical-to-Medical materials. * Independently perform fact-check, scientific review and medical approval of promotional and medical materials and activities in line with local product label information, country-specific code and regulatory requirements.
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                        Our partner is looking for a Lab Operations Project Engineer to join its team. Lab Operations Project Engineering entails being responsible for the compliance assessment of method validation and compendial compliance dossiers. This service involves the careful implementation of new test methods and procedures in Quality Control Operations, including coordinating and planning project activities. * Implementation of new test methods and procedures in Quality Control Operations * Coordination and planning of project activities * Jefferson Wells * PUURS * Vast contract, onbepaalde tijd * Voltijds - Antwerp – Contracting - This international company is well known for its pharmaceuticals. Your responsibilities * Writing and reviewing protocols, testing scripts, and reports * Management of deviations * Review of validation and transfer test results * Validation of necessary files (e.g., SoftMaxPro, Excel)
                        Our partner is looking for a Lab Operations Project Engineer to join its team. Lab Operations Project Engineering entails being responsible for the compliance assessment of method validation and compendial compliance dossiers. This service involves the careful implementation of new test methods and procedures in Quality Control Operations, including coordinating and planning project activities. * Implementation of new test methods and procedures in Quality Control Operations * Coordination and planning of project activities * Jefferson Wells * PUURS * Vast contract, onbepaalde tijd * Voltijds - Antwerp – Contracting - This international company is well known for its pharmaceuticals. Your responsibilities * Writing and reviewing protocols, testing scripts, and reports * Management of deviations * Review of validation and transfer test results * Validation of necessary files (e.g., SoftMaxPro, Excel)
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                        Provide technical insights gleaned from the market to help guide new application developments. This powerful combination produces polymers that have the capability to outperform today's thermoset composite solutions across a broad set of everyday applications such as wind turbine blades, electric vehicle parts, construction, and anticorrosion coatings. Your role is to help prospective customers around the world convert from their existing thermoset products to ProxximaTM polyolefin thermoset systems by demonstrating cycle time, weight, and physical performance advantages on their composite fabrication equipment. * Provide on-site technical support for customers producing composites via vacuum assisted (VA) and high pressure (HP) resin transfer molding (RTM), pultrusion, and filament winding processes. * Provide on-site technical support for customers producing ...
                        Provide technical insights gleaned from the market to help guide new application developments. This powerful combination produces polymers that have the capability to outperform today's thermoset composite solutions across a broad set of everyday applications such as wind turbine blades, electric vehicle parts, construction, and anticorrosion coatings. Your role is to help prospective customers around the world convert from their existing thermoset products to ProxximaTM polyolefin thermoset systems by demonstrating cycle time, weight, and physical performance advantages on their composite fabrication equipment. * Provide on-site technical support for customers producing composites via vacuum assisted (VA) and high pressure (HP) resin transfer molding (RTM), pultrusion, and filament winding processes. * Provide on-site technical support for customers producing ...
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                        NIEUW
                        The Director Strategic Development & New Installations is responsible and accountable for the organisation and the working of his process. * More specifically, the Director Strategic Development & New Installations would be in charge of prelicensing and licensing of regulatory and non-regulatory projects as well as developing non regulatory projects. * The Director Strategic Development & New Installations is Line Manager for the attached to his process (mid-management level) and is a.o. in charge of the development and evaluation of his . * The Director Strategic Development & New Installations is a Senior Management position and reports to the . * Bel V is an integral part of the Belgian nuclear safety authority. The Federal Agency for Nuclear Control (FANC) delegates to us the task of carrying out regulatory inspections and safety assessments of the most important nuclear installations in Belgium.
                        The Director Strategic Development & New Installations is responsible and accountable for the organisation and the working of his process. * More specifically, the Director Strategic Development & New Installations would be in charge of prelicensing and licensing of regulatory and non-regulatory projects as well as developing non regulatory projects. * The Director Strategic Development & New Installations is Line Manager for the attached to his process (mid-management level) and is a.o. in charge of the development and evaluation of his . * The Director Strategic Development & New Installations is a Senior Management position and reports to the . * Bel V is an integral part of the Belgian nuclear safety authority. The Federal Agency for Nuclear Control (FANC) delegates to us the task of carrying out regulatory inspections and safety assessments of the most important nuclear installations in Belgium.
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                        Je hebt een bachelor diploma in chemie, biochemie, industriële wetenschappen of farmaceutische laboratoriumtechnieken en/of beschikt over relevante werkervaring in een analytisch labo * Stegmann Belgium (BVBA) * Antwerpen * Interimwerk met optie 'vast werk' * Voltijds - Solliciteer als één van de eersten - Jouw verantwoordelijkheden - Wat ga je doen? Staalvoorbereiding en bepalen van metalen op diverse voedings- en milieustalen met behulp van technieken zoals CV-AAS, ICP-OES, ICP-MS, ICP-SF-MS - Kwaliteitscontrole en meedenken over methode-ontwikkeling en procesverbeteringen - Verwerking van chromatografische data en rapportage van resultaten - Zorg dragen voor het onderhoud van de laboratoriuminstrumenten - Jouw profiel - Kennis van ICP-technieken is uiteraard een groot pluspunt. Je werkt nauwkeurig, zelfstandig, bent communicatief en kan goed omgaan met deadlines
                        Je hebt een bachelor diploma in chemie, biochemie, industriële wetenschappen of farmaceutische laboratoriumtechnieken en/of beschikt over relevante werkervaring in een analytisch labo * Stegmann Belgium (BVBA) * Antwerpen * Interimwerk met optie 'vast werk' * Voltijds - Solliciteer als één van de eersten - Jouw verantwoordelijkheden - Wat ga je doen? Staalvoorbereiding en bepalen van metalen op diverse voedings- en milieustalen met behulp van technieken zoals CV-AAS, ICP-OES, ICP-MS, ICP-SF-MS - Kwaliteitscontrole en meedenken over methode-ontwikkeling en procesverbeteringen - Verwerking van chromatografische data en rapportage van resultaten - Zorg dragen voor het onderhoud van de laboratoriuminstrumenten - Jouw profiel - Kennis van ICP-technieken is uiteraard een groot pluspunt. Je werkt nauwkeurig, zelfstandig, bent communicatief en kan goed omgaan met deadlines
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                        Naast microbiologie worden deze technieken in ons biochemisch lab verder uitgediept voor de bepaling van allergenen, GGO's en species identificatie. * Om onze activiteiten zo goed mogelijk op onze klanten af te stemmen, werkt het labo microbiologie ook verder in het weekend. Indien je al relevante ervaring hebt opgedaan in een labo microbiologie, heb je uiteraard een streepje voor. * SGS Group Belgium * Antwerpen * Vast contract, onbepaalde tijd * Voltijds - Bedrijfsomschrijving - When you need to be sure, dat is waar SGS voor staat. Bij SGS bieden wij jou namelijk double layer sureness, dubbellaagse zekerheid. Als wereldleider op het gebied van inspectie, controle, analyse en certificering, staan wij garant voor kwaliteit en integriteit. Wereldwijd telt de SGS-familie bijna 100.000 enthousiaste medewerkers. In België geven ca 1850 collega's dagelijks het beste van zichzelf om onze klanten zo efficiënt en ...
                        Naast microbiologie worden deze technieken in ons biochemisch lab verder uitgediept voor de bepaling van allergenen, GGO's en species identificatie. * Om onze activiteiten zo goed mogelijk op onze klanten af te stemmen, werkt het labo microbiologie ook verder in het weekend. Indien je al relevante ervaring hebt opgedaan in een labo microbiologie, heb je uiteraard een streepje voor. * SGS Group Belgium * Antwerpen * Vast contract, onbepaalde tijd * Voltijds - Bedrijfsomschrijving - When you need to be sure, dat is waar SGS voor staat. Bij SGS bieden wij jou namelijk double layer sureness, dubbellaagse zekerheid. Als wereldleider op het gebied van inspectie, controle, analyse en certificering, staan wij garant voor kwaliteit en integriteit. Wereldwijd telt de SGS-familie bijna 100.000 enthousiaste medewerkers. In België geven ca 1850 collega's dagelijks het beste van zichzelf om onze klanten zo efficiënt en ...
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                        The Laboratory Technician will be responsible for the routine production of micro-organisms and the execution of quality control (QC) analyses in accordance with established procedures and production schedules. * Maintain high standards of laboratory safety, cleanliness, and organization in accordance with company policies and regulatory guidelines. * Strong understanding of microbiological techniques and laboratory best practices. * Jefferson Wells * Nevele * Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - Contracting – Deinze - The role requires strong technical expertise in microbiological techniques, strict adherence to safety and quality standards, and effective collaboration within a multidisciplinary team environment. Your responsibilities - Key Responsibilities * Perform and document routine production of micro-organisms in compliance with approved procedures and planning.
                        The Laboratory Technician will be responsible for the routine production of micro-organisms and the execution of quality control (QC) analyses in accordance with established procedures and production schedules. * Maintain high standards of laboratory safety, cleanliness, and organization in accordance with company policies and regulatory guidelines. * Strong understanding of microbiological techniques and laboratory best practices. * Jefferson Wells * Nevele * Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - Contracting – Deinze - The role requires strong technical expertise in microbiological techniques, strict adherence to safety and quality standards, and effective collaboration within a multidisciplinary team environment. Your responsibilities - Key Responsibilities * Perform and document routine production of micro-organisms in compliance with approved procedures and planning.
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                        Grijp dan deze kans om de R&D-afdeling vorm te geven en direct impact te hebben. * Ceres Recruitment * Brecht * Vast contract, onbepaalde tijd * Voltijds - Introductie - Wil jij de Belgische klassiekers zoals stoofvlees en vol-au-vent naar een hoger niveau tillen? Krijg je energie van nieuwe productcategorieën te ontwikkelen? Coertjens - Coertjens is een Belgische voedingsproducent met roots die teruggaan tot 1956, waar het begon als ambachtelijke beenhouwerij. Doorheen de jaren groeide het bedrijf uit tot een moderne organisatie met productiesites in Brecht en Luik. Het bedrijf blijft inspelen op veranderende markten via innovatie, nieuwe productcategorieën en nieuwe marktsegmenten. Wil je deel uitmaken van een managementteam waar uw ideeën ertoe doen en innovatie ruimte krijgt? Jouw verantwoordelijkheden - Jij maakt smaak schaalbaar * Het ontwikkelen van nieuwe producten en categorieën.
                        Grijp dan deze kans om de R&D-afdeling vorm te geven en direct impact te hebben. * Ceres Recruitment * Brecht * Vast contract, onbepaalde tijd * Voltijds - Introductie - Wil jij de Belgische klassiekers zoals stoofvlees en vol-au-vent naar een hoger niveau tillen? Krijg je energie van nieuwe productcategorieën te ontwikkelen? Coertjens - Coertjens is een Belgische voedingsproducent met roots die teruggaan tot 1956, waar het begon als ambachtelijke beenhouwerij. Doorheen de jaren groeide het bedrijf uit tot een moderne organisatie met productiesites in Brecht en Luik. Het bedrijf blijft inspelen op veranderende markten via innovatie, nieuwe productcategorieën en nieuwe marktsegmenten. Wil je deel uitmaken van een managementteam waar uw ideeën ertoe doen en innovatie ruimte krijgt? Jouw verantwoordelijkheden - Jij maakt smaak schaalbaar * Het ontwikkelen van nieuwe producten en categorieën.
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                        Wat is het gemiddelde salaris voor Cro in Waver?

                        Gemiddeld salaris per jaar
                        42.100 €

                        Het salaris gemiddelde voor een Cro in Waver is 42.100 €. De salarissen van Cro in Waver variëren van 35.100 € tot 51.300 €.