Science jobs

The University of Luxembourg (UL) is recruiting for the following position at the Luxembourg Learning Centre: Librarian Specialist Since that day to now its spaces and collections have faced several challenging issues which require a specialist on disaster planning, response and recovery. University of Luxembourg Competence Centre * Luxembourg * Contract duration specified * Full Time - Introduction * Fixed-term contract (6 months) * Full time (40h/week) * Starting: as soon as possible * Employee status - In September 2018, the Luxembourg Learning Centre (LLC) opened its doors to the public. Your role * Develop a Risk Assessment Plan to evaluate and mitigate the actual and potential threats to the LLC and its collections * Draft a Business Continuity Plan as a response tool for services provision and access to resources in case of an emergency at the LLC The University of Luxembourg (UL) is recruiting for the following position at the Luxembourg Learning Centre: Librarian Specialist Since that day to now its spaces and collections have faced several challenging issues which require a specialist on disaster planning, response and recovery. University of Luxembourg Competence Centre * Luxembourg * Contract duration specified * Full Time - Introduction * Fixed-term contract (6 months) * Full time (40h/week) * Starting: as soon as possible * Employee status - In September 2018, the Luxembourg Learning Centre (LLC) opened its doors to the public. Your role * Develop a Risk Assessment Plan to evaluate and mitigate the actual and potential threats to the LLC and its collections * Draft a Business Continuity Plan as a response tool for services provision and access to resources in case of an emergency at the LLC
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For one of the SGS Life Sciences departments, Exprimo, we are looking for an Experienced Modeling & Simulation Scientist SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Introduction - At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call 'connectors', people who can connect our diversity to our services. To each other. And this way, enrich our business. 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. For one of the SGS Life Sciences departments, Exprimo, we are looking for an Experienced Modeling & Simulation Scientist SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Introduction - At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call 'connectors', people who can connect our diversity to our services. To each other. And this way, enrich our business. 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.
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You have experience in regulatory affairs in the pharma sector? You have deep knowledge of Regulatory Affairs in different geographical areas. Our partner is looking for a RA Manager to join its team. As RA Manager, you will bring support for CMC. * for key regulatory activities pertaining to a project/product. * Provide in-depth input into the asset specific regulatory strategy on a global scale for technical/CMC and procedural aspects. * via critical review of the technical and procedural section of regulatory documents * Coordinate (for technical/CMC and procedural part) the determination of key messages for product/portfolio specific regulatory documents to be submitted to Authorities, * Compile/write high quality project/product specific regulatory documents to be submitted to Authorities (for technical/CMC and procedural sections) and ensure that those documents meet regulatory requirements. You have experience in regulatory affairs in the pharma sector? You have deep knowledge of Regulatory Affairs in different geographical areas. Our partner is looking for a RA Manager to join its team. As RA Manager, you will bring support for CMC. * for key regulatory activities pertaining to a project/product. * Provide in-depth input into the asset specific regulatory strategy on a global scale for technical/CMC and procedural aspects. * via critical review of the technical and procedural section of regulatory documents * Coordinate (for technical/CMC and procedural part) the determination of key messages for product/portfolio specific regulatory documents to be submitted to Authorities, * Compile/write high quality project/product specific regulatory documents to be submitted to Authorities (for technical/CMC and procedural sections) and ensure that those documents meet regulatory requirements.
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In the context of its missions in clinical studies, Labo'Life Belgium, a pharmaceutical company specialized in micro-immunotherapy, is looking for a Junior Clinical Research Associate, in June, 2020. * Holder of a scientific background, you dispose of a Clinical Research training (UD/ Master in Clinical Research / Private Training), good regulatory and GCPs knowledge. This permanent position will be based in Namur (Belgium), and depends on the French Clinical Department of the group. For now, all clinical trials are performed in Belgium. Your missions as Junior CRA * Assist in writing clinical study protocols, case report forms, patient diaries, … * Carry out follow-up visits for clinical studies (data verification with the patient's source file), * Verify the treatment units, products and materials dispensing for clinical studies, * Archive clinical study documentation, administrative and regulatory documents, In the context of its missions in clinical studies, Labo'Life Belgium, a pharmaceutical company specialized in micro-immunotherapy, is looking for a Junior Clinical Research Associate, in June, 2020. * Holder of a scientific background, you dispose of a Clinical Research training (UD/ Master in Clinical Research / Private Training), good regulatory and GCPs knowledge. This permanent position will be based in Namur (Belgium), and depends on the French Clinical Department of the group. For now, all clinical trials are performed in Belgium. Your missions as Junior CRA * Assist in writing clinical study protocols, case report forms, patient diaries, … * Carry out follow-up visits for clinical studies (data verification with the patient's source file), * Verify the treatment units, products and materials dispensing for clinical studies, * Archive clinical study documentation, administrative and regulatory documents,
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Our partner is looking for a Technician PCMD HPLC-UPLC to join its team. Experis * Wallonia * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Participate in development of analytical methods * Participate in (co-)validation or verification of analytical methods. * Analyse results * Verify data * Perform daily laboratory activities related to release and stability testing * Follow up deviations, incidents and validate the results. * Participate to method transfers from different laboratories * Participate in writing the documentation related to the lab activities - Your profile - Who are you? * Bachelor's degree, or master's degree, in biochemistry or in analytical chemistry or in biology. * Previous experience preferably in the biotech industry * Good knowledge of development and validations of analytical method * Strong and proven laboratory skills Our partner is looking for a Technician PCMD HPLC-UPLC to join its team. Experis * Wallonia * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Participate in development of analytical methods * Participate in (co-)validation or verification of analytical methods. * Analyse results * Verify data * Perform daily laboratory activities related to release and stability testing * Follow up deviations, incidents and validate the results. * Participate to method transfers from different laboratories * Participate in writing the documentation related to the lab activities - Your profile - Who are you? * Bachelor's degree, or master's degree, in biochemistry or in analytical chemistry or in biology. * Previous experience preferably in the biotech industry * Good knowledge of development and validations of analytical method * Strong and proven laboratory skills
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for Belgium finance and sales admin.) (Belgium only) Monitor the car sales contract status in the system. countersign within 24 hours once a new sales contract is sent by the customer. (Only - Demonstrated understanding of automotive finance related processes - Experis * Brussels * Freelance * Full Time - Your responsibilities (Sweden, Norway, Belgium only) Verify customer's financing applications, loan - agreements from various banks in local language. Extract potential information that is - needed for the financing process from those documents. Contact these various - banks for more information if needed. Communicate with the customer in case of - queries. Update order with payment terms & payment party master data in the - systems. Secure a - Follow up on invoices, i.e. space investors, providers of - delivery services and workshops by making sure that they are accurate and in line - with what has been agreed. for Belgium finance and sales admin.) (Belgium only) Monitor the car sales contract status in the system. countersign within 24 hours once a new sales contract is sent by the customer. (Only - Demonstrated understanding of automotive finance related processes - Experis * Brussels * Freelance * Full Time - Your responsibilities (Sweden, Norway, Belgium only) Verify customer's financing applications, loan - agreements from various banks in local language. Extract potential information that is - needed for the financing process from those documents. Contact these various - banks for more information if needed. Communicate with the customer in case of - queries. Update order with payment terms & payment party master data in the - systems. Secure a - Follow up on invoices, i.e. space investors, providers of - delivery services and workshops by making sure that they are accurate and in line - with what has been agreed.
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Receiving the possibility to develop yourself as a clinical professional shouldered by our company's five core values, you'll add value to our customer's team that goes beyond your scientific and technical skills. * Ensure clinical trials are SOPs and applicable guidelines and regulations * Ensure proper training of the site's study team on the clinical project and adherence to applicable guidelines and regulations * Manage distribution and return of clinical trial supplies (incl. investigational product) * Belgium * Contract duration unspecified * Full Time - Introduction - Being a CRA at Fern Valley means becoming part of a group of high quality specialists. Note that throughout this journey you will never be alone; personal contact, follow-up, training and career planning are of the utmost importance to us. Receiving the possibility to develop yourself as a clinical professional shouldered by our company's five core values, you'll add value to our customer's team that goes beyond your scientific and technical skills. * Ensure clinical trials are SOPs and applicable guidelines and regulations * Ensure proper training of the site's study team on the clinical project and adherence to applicable guidelines and regulations * Manage distribution and return of clinical trial supplies (incl. investigational product) * Belgium * Contract duration unspecified * Full Time - Introduction - Being a CRA at Fern Valley means becoming part of a group of high quality specialists. Note that throughout this journey you will never be alone; personal contact, follow-up, training and career planning are of the utmost importance to us.
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As a R&D Engineer Industrialisation you have a good chemical knowledge and the attitude to enlarge this knowledge within the working domain. * Be actively involved in providing technical support on supply chain industrialisation project. McBride * Estaimpuis * Contract duration unspecified * Full Time - McBride is the leading European manufacturer and supplier of Contract Manufactured and Private Label products for the domestic and professional cleaning/hygiene markets. Headquartered in Manchester, UK, McBride operates across twelve countries, with 16 manufacturing facilities producing over 1.2 billion units a year, and employs 4,000 people globally. Established in 1927, McBride boasts a strong heritage. We are the private label experts in our segments, with the scale to offer our development and manufacturing capabilities to customers in the UK, Continental Europe and Asia Pacific. As a R&D Engineer Industrialisation you have a good chemical knowledge and the attitude to enlarge this knowledge within the working domain. * Be actively involved in providing technical support on supply chain industrialisation project. McBride * Estaimpuis * Contract duration unspecified * Full Time - McBride is the leading European manufacturer and supplier of Contract Manufactured and Private Label products for the domestic and professional cleaning/hygiene markets. Headquartered in Manchester, UK, McBride operates across twelve countries, with 16 manufacturing facilities producing over 1.2 billion units a year, and employs 4,000 people globally. Established in 1927, McBride boasts a strong heritage. We are the private label experts in our segments, with the scale to offer our development and manufacturing capabilities to customers in the UK, Continental Europe and Asia Pacific.
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Our partner is looking for a Technician PCMD (Physico-Chemical Method Development) Electrophoresis to join its team. Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Participate in development of analytical methods * Participate in (co-)validation or verification of analytical methods. * Analyze results * Verify data * Perform daily laboratory activities related to release and stability testing * Follow up deviations, incidents and validate the results. * Participate to method transfers from different laboratories * Participate in writing the documentation related to the lab activities - Your profile - Who are you? * Bachelor's degree, or master's degree, in biochemistry or in analytical chemistry or in biology. * Previous experience preferably in the biotech industry * Good knowledge of development and validations of analytical method Our partner is looking for a Technician PCMD (Physico-Chemical Method Development) Electrophoresis to join its team. Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Participate in development of analytical methods * Participate in (co-)validation or verification of analytical methods. * Analyze results * Verify data * Perform daily laboratory activities related to release and stability testing * Follow up deviations, incidents and validate the results. * Participate to method transfers from different laboratories * Participate in writing the documentation related to the lab activities - Your profile - Who are you? * Bachelor's degree, or master's degree, in biochemistry or in analytical chemistry or in biology. * Previous experience preferably in the biotech industry * Good knowledge of development and validations of analytical method
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As a member of our central Internal Control team in Risk Management, you work in a cross-cutting team assisting all departments of AXA Belgium as a second line of defence. The members of the team are primarily occupied with their specialisation, and thus guarantee the various frameworks for internal control associated with this specialisation. They demonstrate a critical analytical mind, allowing them to identify the significant risks faced by a business entity and to ensure that the necessary front-line controls to mitigate the risks are carried out and produce the expected results. * Monitoring the effectiveness of the processes and controls put in place by Business Line in order to mitigate the main risks associated with them and to provide advice to improve the effectiveness of control systems. As a member of our central Internal Control team in Risk Management, you work in a cross-cutting team assisting all departments of AXA Belgium as a second line of defence. The members of the team are primarily occupied with their specialisation, and thus guarantee the various frameworks for internal control associated with this specialisation. They demonstrate a critical analytical mind, allowing them to identify the significant risks faced by a business entity and to ensure that the necessary front-line controls to mitigate the risks are carried out and produce the expected results. * Monitoring the effectiveness of the processes and controls put in place by Business Line in order to mitigate the main risks associated with them and to provide advice to improve the effectiveness of control systems.
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In light of their further growth and professionalization of the Complaint Handling Process we are looking for a Senior Post Market Specialist EMEA, with a strong background in In Vitro Diagnostics. * 5 years of experience as Post Market Specialist, Complaint Handling Specialist or Regulatory Compliance in a manufacturing environment, preferably in in-vitro diagnostics * Providing training on the requirements related to Authority reporting, complaint handling process and Post Market Requirements to internal stakeholders * Supporting of the Post-Market Surveillance activities in alignment with regulatory requirements - Motmans & Partners * Tessenderlo * Contract duration unspecified * Full Time - Tosoh Corporation is part of a Japanese chemical and specialty products and materials group that comprises over 130 companies worldwide and a multiethnic workforce of more than 12,000 people. In light of their further growth and professionalization of the Complaint Handling Process we are looking for a Senior Post Market Specialist EMEA, with a strong background in In Vitro Diagnostics. * 5 years of experience as Post Market Specialist, Complaint Handling Specialist or Regulatory Compliance in a manufacturing environment, preferably in in-vitro diagnostics * Providing training on the requirements related to Authority reporting, complaint handling process and Post Market Requirements to internal stakeholders * Supporting of the Post-Market Surveillance activities in alignment with regulatory requirements - Motmans & Partners * Tessenderlo * Contract duration unspecified * Full Time - Tosoh Corporation is part of a Japanese chemical and specialty products and materials group that comprises over 130 companies worldwide and a multiethnic workforce of more than 12,000 people.
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As the Application Specialist you Cleaning Solutions. * At least 5 years of B2B experience in a function like e.g. Product or Project Manager, Innovation Lead, Product Specialist. Ceres Recruitment * Ghent, Belgium * Contract duration unspecified * Full Time - Introduction - DeLaval (part of Tetra Laval Group) is a world leader in the dairy farming industry, providing integrated milking solutions designed to improve dairy farmers' production, animal welfare and overall quality of life. They are a group of over 4500 passionate professionals operating in more than 100 markets across the globe. They in partnership to realize their vision of making sustainable food production possible. DeLaval offers automatic and conventional milking systems, cooling and feeding systems, effluent & housing systems and farm management support systems. As the Application Specialist you Cleaning Solutions. * At least 5 years of B2B experience in a function like e.g. Product or Project Manager, Innovation Lead, Product Specialist. Ceres Recruitment * Ghent, Belgium * Contract duration unspecified * Full Time - Introduction - DeLaval (part of Tetra Laval Group) is a world leader in the dairy farming industry, providing integrated milking solutions designed to improve dairy farmers' production, animal welfare and overall quality of life. They are a group of over 4500 passionate professionals operating in more than 100 markets across the globe. They in partnership to realize their vision of making sustainable food production possible. DeLaval offers automatic and conventional milking systems, cooling and feeding systems, effluent & housing systems and farm management support systems.
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For its Public Affairs department, Cefic is looking for a (m/f/x) Advocacy & Regulatory Affairs Manager Working closely with a dynamic team of public affairs professionals, the manager will provide advocacy support to the Specialty Chemicals Sector Groups of Cefic, with a focus on chemical legislations and particular attention to REACH and CLP Regulations. * Contribute to the development of advocacy strategies, actively implementing the plans either individually or as part of a wider team; * Provide advocacy support to different Sector Groups on a variety of challenging but interesting topics; * Provide regulatory & political guidance to the Sector Groups by shedding light on the complex regulatory processes involved in the different chemical regulations; For its Public Affairs department, Cefic is looking for a (m/f/x) Advocacy & Regulatory Affairs Manager Working closely with a dynamic team of public affairs professionals, the manager will provide advocacy support to the Specialty Chemicals Sector Groups of Cefic, with a focus on chemical legislations and particular attention to REACH and CLP Regulations. * Contribute to the development of advocacy strategies, actively implementing the plans either individually or as part of a wider team; * Provide advocacy support to different Sector Groups on a variety of challenging but interesting topics; * Provide regulatory & political guidance to the Sector Groups by shedding light on the complex regulatory processes involved in the different chemical regulations;
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The locally recruited teachers are hired under the employee status to teach in the secondary cycle. * Removal costs : in accordance to the Service regulations, the locally recruited teachers recruited for a minimum period of one year and a contract providing a minimum of 16 hours/periods per week, are entitled to reimbursement of their removal expenses unless the contract ends within the first 12 months due to circumstances lying in their responsibility (cfr: article 37 & 38 of the Service regulations). The locally recruited teachers are hired under the employee status to teach in the secondary cycle. * Removal costs : in accordance to the Service regulations, the locally recruited teachers recruited for a minimum period of one year and a contract providing a minimum of 16 hours/periods per week, are entitled to reimbursement of their removal expenses unless the contract ends within the first 12 months due to circumstances lying in their responsibility (cfr: article 37 & 38 of the Service regulations).
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With a growing mentality they are expanding their risk management department and are urgently looking for a Quantitative Risk officer to join their team. Do you have a previous experience in Risk management? If you are ready for the next step in your risk career then this company can definitely offer you an interesting perspective. * Risk management linked to quantitative risks * You have minimum 3 years of experience in a risk management function - James Woodman * Brussels * Contract duration unspecified * Full Time - Are you currently looking for a new opportunity? Do you like to be surrounded by motivated and dynamic co-workers? Then this job is the one you've been looking for! This company is very well-known in the Belgium insurance sector. If you want to find out more about this opportunity don't hesitate to apply and send me your resume. * Quantitative work With a growing mentality they are expanding their risk management department and are urgently looking for a Quantitative Risk officer to join their team. Do you have a previous experience in Risk management? If you are ready for the next step in your risk career then this company can definitely offer you an interesting perspective. * Risk management linked to quantitative risks * You have minimum 3 years of experience in a risk management function - James Woodman * Brussels * Contract duration unspecified * Full Time - Are you currently looking for a new opportunity? Do you like to be surrounded by motivated and dynamic co-workers? Then this job is the one you've been looking for! This company is very well-known in the Belgium insurance sector. If you want to find out more about this opportunity don't hesitate to apply and send me your resume. * Quantitative work
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As Biologic Product Development Lead, you are in charge to - o Lead Failure Mode and Effect Analysis (FMEA) for the drug product formulation, fill and finish process; o Define and follow the implementation of the needed laboratory area and equipment to perform biological drug product formulation development, drug product process development and scale-ups; o Collaborate with universities / research centers to ensure up-to-date knowledge of biological drug product development and manufacturing; o According to increasing customers' demand, create and manage a team for the drug product development. You have an experience in process scale for Biological drug product development including formulation development and drug product process development and an experience in Biological drug product formulation validation, process scale up, and technology transfer. As Biologic Product Development Lead, you are in charge to - o Lead Failure Mode and Effect Analysis (FMEA) for the drug product formulation, fill and finish process; o Define and follow the implementation of the needed laboratory area and equipment to perform biological drug product formulation development, drug product process development and scale-ups; o Collaborate with universities / research centers to ensure up-to-date knowledge of biological drug product development and manufacturing; o According to increasing customers' demand, create and manage a team for the drug product development. You have an experience in process scale for Biological drug product development including formulation development and drug product process development and an experience in Biological drug product formulation validation, process scale up, and technology transfer.
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For its Catchment & eco-hydrology research group, the ERIN department has an opening for a permanent position for a laboratory technician in hydro-chemistry and analyses of stable isotopes of O and H in water. * Vocational training in analytical chemistry (e.g. chemistry laboratory technician, level BAC+2/3) and practical experience in water analytical chemistry are a requirement - Fix minor issues with laboratory equipment and in case of major equipment failures. Make regular updates on material and supplies required for a flawless operation of laboratory activities. * Pay great attention and respect to 'Health & Security Environment' protocols in force at LIST and participate actively in the general organisation of the department's laboratories, including waste management, implementation of safety measures, contact with lab material providers, general maintenance of lab infrastructure, etc. For its Catchment & eco-hydrology research group, the ERIN department has an opening for a permanent position for a laboratory technician in hydro-chemistry and analyses of stable isotopes of O and H in water. * Vocational training in analytical chemistry (e.g. chemistry laboratory technician, level BAC+2/3) and practical experience in water analytical chemistry are a requirement - Fix minor issues with laboratory equipment and in case of major equipment failures. Make regular updates on material and supplies required for a flawless operation of laboratory activities. * Pay great attention and respect to 'Health & Security Environment' protocols in force at LIST and participate actively in the general organisation of the department's laboratories, including waste management, implementation of safety measures, contact with lab material providers, general maintenance of lab infrastructure, etc.
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