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SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Company Description - At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice.
SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Company Description - At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice.
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He/she spends a lot of time in production, supporting the several shifts in handling the daily operational issues, keeping an overall eye on the performances of those shifts and being a contact person and voice for other departments.
He/she spends a lot of time in production, supporting the several shifts in handling the daily operational issues, keeping an overall eye on the performances of those shifts and being a contact person and voice for other departments.
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In addition to the above mentioned activities, the Secure Data Manager will also be responsible for the handling of randomisation lists (upload of randomisation list in internal IWRS system, release of randomisation list at database lock, emergency unblindings, distribution of randomisation list to third parties,…).
In addition to the above mentioned activities, the Secure Data Manager will also be responsible for the handling of randomisation lists (upload of randomisation list in internal IWRS system, release of randomisation list at database lock, emergency unblindings, distribution of randomisation list to third parties,…).
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Serious Adverse Events/Adverse Drugs Reactions (SAEs/ADRs) handling (Clinical Trial and Post Marketing) including review of SAEs/ ADRs, performing regulatory assessments and in order to have events fully documented
Serious Adverse Events/Adverse Drugs Reactions (SAEs/ADRs) handling (Clinical Trial and Post Marketing) including review of SAEs/ ADRs, performing regulatory assessments and in order to have events fully documented
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We are currently looking for Clinical Data Managers (Mechelen). You will be in charge of data cleaning of clinical subject databases. You check clinical databases on inconsistent, missing and incorrect data and make sure mistakes are found either way; SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. will define the cleaning package of a clinical trial; You will generate queries towards the sites to get the data clean and will not give up until you reach your goal; you love to communicate with all involved parties. You have obtained a Master's Degree in a paramedical area or biomedical sciences. SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time
We are currently looking for Clinical Data Managers (Mechelen). You will be in charge of data cleaning of clinical subject databases. You check clinical databases on inconsistent, missing and incorrect data and make sure mistakes are found either way; SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. will define the cleaning package of a clinical trial; You will generate queries towards the sites to get the data clean and will not give up until you reach your goal; you love to communicate with all involved parties. You have obtained a Master's Degree in a paramedical area or biomedical sciences. SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time
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We currently have an opportunity for a Medical Writer! SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Company Description - 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. Our coworkers build their own way inside the company, the services and the expertise.
We currently have an opportunity for a Medical Writer! SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Company Description - 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. Our coworkers build their own way inside the company, the services and the expertise.
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My clients Regulatory & Product Support Department is seeking a dynamic Regulatory Associate to join their team. You will work in cross-functional teams with different Puurs departments (manufacturing, labs, QA, supply,…) and collaborate with R&D, global regulatory colleagues (Global Chemistry, Manufacturing & Controls (GCMC)) and the supply department in order to support the introduction of new products in the site. * You support regulatory submissions (CTD, BLA) of the products by informing site colleagues of regulatory requirements and by authoring the dossier, for review with GCMC. In this regulatory role you interact on a daily basis with several Puurs departments (manufacturing, labs, QA, supply,…). * You assess Post approval changes at the manufacturing site and the associated regulatory variations.
My clients Regulatory & Product Support Department is seeking a dynamic Regulatory Associate to join their team. You will work in cross-functional teams with different Puurs departments (manufacturing, labs, QA, supply,…) and collaborate with R&D, global regulatory colleagues (Global Chemistry, Manufacturing & Controls (GCMC)) and the supply department in order to support the introduction of new products in the site. * You support regulatory submissions (CTD, BLA) of the products by informing site colleagues of regulatory requirements and by authoring the dossier, for review with GCMC. In this regulatory role you interact on a daily basis with several Puurs departments (manufacturing, labs, QA, supply,…). * You assess Post approval changes at the manufacturing site and the associated regulatory variations.
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In the spirit of continued growth and to help improve our business, we are currently seeking for a Clinical Research Coordinator. SGS Group Belgium * Antwerpen * Contract duration unspecified * Full Time - Company Description - 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.
In the spirit of continued growth and to help improve our business, we are currently seeking for a Clinical Research Coordinator. SGS Group Belgium * Antwerpen * Contract duration unspecified * Full Time - Company Description - 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 will be working as a Data Analytics Intern in the Sales and Operations department at Bosch Thermotechnology in Mechelen. You will maintain and harmonize the data present in different applications. You are currently a student (International Business Management, Marketing, Economical Studies, etc.) or you recently graduated, and you are interested in Data Analysis and Business Intelligence. If you are a student enrolled in a University/College outside of Belgium (or if you are available for a voluntary internship outside of your university curriculum) you will be granted an allowance of € 850/month. Robert Bosch NV/SA * Mechelen * Contract duration unspecified * Full Time - Smart and efficient – Bosch Thermotechnology offers its customers throughout the world solutions for their room climate, domestic hot water and decentralised energy management requirements.
You will be working as a Data Analytics Intern in the Sales and Operations department at Bosch Thermotechnology in Mechelen. You will maintain and harmonize the data present in different applications. You are currently a student (International Business Management, Marketing, Economical Studies, etc.) or you recently graduated, and you are interested in Data Analysis and Business Intelligence. If you are a student enrolled in a University/College outside of Belgium (or if you are available for a voluntary internship outside of your university curriculum) you will be granted an allowance of € 850/month. Robert Bosch NV/SA * Mechelen * Contract duration unspecified * Full Time - Smart and efficient – Bosch Thermotechnology offers its customers throughout the world solutions for their room climate, domestic hot water and decentralised energy management requirements.
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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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Antwerpen * Contract duration unspecified * Full Time - Your responsibilities - Als betrouwbare sta je mee aan het roer van de afdeling Microbiologie en ben je verantwoordelijk voor de dagelijkse operationele activiteiten. * Dankzij jouw labo ervaring en analytisch inzicht kan je snel en efficiënt alle routinematige en nieuwe analyseopdrachten beoordelen op uitvoerbaarheid. * Je verdiept je in mogelijke nieuwe labo toepassingen en opzetten van nieuwe analysemethodes, waardoor onze dienstverlening nog breder en professioneler wordt. Hierbij leg je steeds de focus op kwaliteit, veiligheid en permanente efficiëntieverbetering. * Vooraleer de analyseresultaten en bijhorende rapporten onze klant worden doorgestuurd, kijk je deze nog even na op mogelijke fouten of onregelmatigheden.
Antwerpen * Contract duration unspecified * Full Time - Your responsibilities - Als betrouwbare sta je mee aan het roer van de afdeling Microbiologie en ben je verantwoordelijk voor de dagelijkse operationele activiteiten. * Dankzij jouw labo ervaring en analytisch inzicht kan je snel en efficiënt alle routinematige en nieuwe analyseopdrachten beoordelen op uitvoerbaarheid. * Je verdiept je in mogelijke nieuwe labo toepassingen en opzetten van nieuwe analysemethodes, waardoor onze dienstverlening nog breder en professioneler wordt. Hierbij leg je steeds de focus op kwaliteit, veiligheid en permanente efficiëntieverbetering. * Vooraleer de analyseresultaten en bijhorende rapporten onze klant worden doorgestuurd, kijk je deze nog even na op mogelijke fouten of onregelmatigheden.
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For one of our clients, located in Geel, we are currently looking for a "QA Release Officer". Our client is currently is looking for a candidate with at least a first experience as QA release officer. Oxford Global Resources * Geel * Contract duration specified * Full Time - Your responsibilities - Job Description - Responsibilities * Create deviation list * Review tests * Follow up and reporting of process control * Data verification * Check whether all batch records are closed * Regulatory checks: check in the system whether the relevant countries have approved a specific change, based on this make a list of the countries to which the batch can go. Do the above responsibilities fit you like a glove? and motivation letter via the " " button and you can expect feedback from us soon. Your profile - Requirements * Knowledge of Dutch and English * Knowledge of biotechnological process
For one of our clients, located in Geel, we are currently looking for a "QA Release Officer". Our client is currently is looking for a candidate with at least a first experience as QA release officer. Oxford Global Resources * Geel * Contract duration specified * Full Time - Your responsibilities - Job Description - Responsibilities * Create deviation list * Review tests * Follow up and reporting of process control * Data verification * Check whether all batch records are closed * Regulatory checks: check in the system whether the relevant countries have approved a specific change, based on this make a list of the countries to which the batch can go. Do the above responsibilities fit you like a glove? and motivation letter via the " " button and you can expect feedback from us soon. Your profile - Requirements * Knowledge of Dutch and English * Knowledge of biotechnological process
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ARSANNE Consulting is looking for a Benelux RA, QA and Vigilance Manager for the BENELUX affiliate of an entrepreneurial international pharmaceutical group. Knowledge of BENELUX pharmaceutical regulatory environment is an important asset. * Local Regulatory Contact Person for Marketing Authorizations. Arsanne Consulting SPRL * Brussels * Contract duration unspecified * Full Time - Introduction - Your Mission * You report directly to the General Management and you are responsible for Benelux. * You'll be in charge of the introduction and management of new and existing brands manufactured by the group within the BENELUX market. * Responsible Pharmacist assume the function in relation to GDP (article 12ter of the medicines law of 25 March 1964) as described into Royal Decree of 14 December 2006. * Acts as the local person for medical device distributor in accordance with the legislation of March 18th, 1999.
ARSANNE Consulting is looking for a Benelux RA, QA and Vigilance Manager for the BENELUX affiliate of an entrepreneurial international pharmaceutical group. Knowledge of BENELUX pharmaceutical regulatory environment is an important asset. * Local Regulatory Contact Person for Marketing Authorizations. Arsanne Consulting SPRL * Brussels * Contract duration unspecified * Full Time - Introduction - Your Mission * You report directly to the General Management and you are responsible for Benelux. * You'll be in charge of the introduction and management of new and existing brands manufactured by the group within the BENELUX market. * Responsible Pharmacist assume the function in relation to GDP (article 12ter of the medicines law of 25 March 1964) as described into Royal Decree of 14 December 2006. * Acts as the local person for medical device distributor in accordance with the legislation of March 18th, 1999.
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At the moment for example, we are looking for a quality assurance specialist to consult one of out clients. * Minimum 5 years of experience in a QA-position, preferably in the Pharmaceutical-related Industry - Brunel Belgium NV * Diegem * 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 * 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. * Reporting and follow-up of Quality-KPI's.
At the moment for example, we are looking for a quality assurance specialist to consult one of out clients. * Minimum 5 years of experience in a QA-position, preferably in the Pharmaceutical-related Industry - Brunel Belgium NV * Diegem * 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 * 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. * Reporting and follow-up of Quality-KPI's.
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