Compliance Jobs in Antwerp Province

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LAB ADMIN TECHNICIAN

HAYS

Halle

HAYS is currently looking for a Lab Admin Technician in Flemish-Brabant. The Lab Admin Technician will monitor the general logistics flow of the samples from A to Z. A first experience in a lab environment in a local or international food, pharmaceutical or feed company. * Halle * Contract duration unspecified * Full Time - Your responsibilities * Degree in Food Science * NL/FR/ENG * QA - This means checking the execution of quality sampling plans (micro, analytical, sensorial) to ensure compliance of production environment, process, raw materials, packaging, rework and products in the most efficient way and release conform. You will ensure the execution of quality analysis agreed with customers and send the Certificate of Analysis. documents for raw materials and packaging materials to evaluate conformance. React (disapprove or approve with derogation) and when deviations occur. HAYS is currently looking for a Lab Admin Technician in Flemish-Brabant. The Lab Admin Technician will monitor the general logistics flow of the samples from A to Z. A first experience in a lab environment in a local or international food, pharmaceutical or feed company. * Halle * Contract duration unspecified * Full Time - Your responsibilities * Degree in Food Science * NL/FR/ENG * QA - This means checking the execution of quality sampling plans (micro, analytical, sensorial) to ensure compliance of production environment, process, raw materials, packaging, rework and products in the most efficient way and release conform. You will ensure the execution of quality analysis agreed with customers and send the Certificate of Analysis. documents for raw materials and packaging materials to evaluate conformance. React (disapprove or approve with derogation) and when deviations occur.
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Compliance Engineer

Brunel Belgium NV

Antwerpen

Are you the Compliance Engineer we are looking for? * Update data in compliance follow-up tools ( eg Trackwise, … * Closely work with client's engineers and plant representatives * Awareness of client's compliance procedures by following client's trainings * Approximately 1 to 5 years of experience in pharmaceutical industry in qualification/compliance activities - Brunel Belgium NV * Antwerpen * Contract duration unspecified * Full Time - About You - Does this vacancy match your profile? Don't hesitate and ! Your responsibilities * Changes initiated by production or maintenance * Changes initiated by project engineering groups (MAM , E&PS ) * Periodic reviews on the system's documentation to ensure these systems remain qualified (3year period) * Evaluate calibration deviations and initiate, follow up on and document corrective actions to bring instruments back in compliant condition. * Preparation of intakes. (Sr only) Your profile Are you the Compliance Engineer we are looking for? * Update data in compliance follow-up tools ( eg Trackwise, … * Closely work with client's engineers and plant representatives * Awareness of client's compliance procedures by following client's trainings * Approximately 1 to 5 years of experience in pharmaceutical industry in qualification/compliance activities - Brunel Belgium NV * Antwerpen * Contract duration unspecified * Full Time - About You - Does this vacancy match your profile? Don't hesitate and ! Your responsibilities * Changes initiated by production or maintenance * Changes initiated by project engineering groups (MAM , E&PS ) * Periodic reviews on the system's documentation to ensure these systems remain qualified (3year period) * Evaluate calibration deviations and initiate, follow up on and document corrective actions to bring instruments back in compliant condition. * Preparation of intakes. (Sr only) Your profile
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QA assistant

SGS Group Belgium

Mechelen

In the spirit of continued growth and to help improve our business, we are currently seeking for a QA assistant. As QA assistant in the preparation, audits in accordance with internal procedures. 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. In the spirit of continued growth and to help improve our business, we are currently seeking for a QA assistant. As QA assistant in the preparation, audits in accordance with internal procedures. 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.
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Validation Engineer Computerized Systems

Oxford Global Resources

Geel

For one of our clients in Geel, we are currently looking for a "Validation Engineer Computerized Systems". We are looking for someone who has project experience with the rollout software packages and with sufficient validation experience of Computerized systems / digital tools (e.g. BioLIMS Laboratory Execution System, Electronic flows, ...). * Development, implementation and execution of validation studies for cGMP-critical computerized systems to demonstrate compliance to cGMP-, User- and Regulatory requirements. * Performing validation of systems for which there is industry precedence but standards require interpretation to the particular case and in accordance with cGMP, cGLP and company Procedures. * Generating validation documentation (protocols/reports) and provides assistance with the execution of protocols for computerized systems. * Competent knowledge of Computer Systems Validation For one of our clients in Geel, we are currently looking for a "Validation Engineer Computerized Systems". We are looking for someone who has project experience with the rollout software packages and with sufficient validation experience of Computerized systems / digital tools (e.g. BioLIMS Laboratory Execution System, Electronic flows, ...). * Development, implementation and execution of validation studies for cGMP-critical computerized systems to demonstrate compliance to cGMP-, User- and Regulatory requirements. * Performing validation of systems for which there is industry precedence but standards require interpretation to the particular case and in accordance with cGMP, cGLP and company Procedures. * Generating validation documentation (protocols/reports) and provides assistance with the execution of protocols for computerized systems. * Competent knowledge of Computer Systems Validation
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Clinical Project Manager (Phase II-III)

SGS Group Belgium

Mechelen

As Clinical Project Manager (CPM) at SGS you will provide leadership to a (cross-functional) team in the execution of clinical research projects (late phases). In the spirit of continued growth and to help improve our business, we are currently seeking for a Clinical Project Manager (Phase II-III). * You have at least 2 years of experience in an International Project Management role, having managed international phase 2 and 3 clinical trials in a pharmaceutical or biotech company or another CRO. 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. As Clinical Project Manager (CPM) at SGS you will provide leadership to a (cross-functional) team in the execution of clinical research projects (late phases). In the spirit of continued growth and to help improve our business, we are currently seeking for a Clinical Project Manager (Phase II-III). * You have at least 2 years of experience in an International Project Management role, having managed international phase 2 and 3 clinical trials in a pharmaceutical or biotech company or another CRO. 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.
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Group buyer

Borealis Polymers

Borealis Beringen, Kallo, Zwijndrecht

ensure compliance to the group commodity strategies/established group contracts as well as to the defined procurement processes & procedures - Borealis Polymers * Borealis Beringen, Kallo, Zwijndrecht * Contract duration unspecified * Full Time - We don't just make ground-breaking plastics, chemicals and fertilizers. We make discoveries. Our employees are adventurous, eager to explore and lead the way. They are empowered to aim for new opportunities and uncover ground-breaking solutions. Each member of the Borealis team makes a difference, adding value for our customers and society as a whole. Join our dynamic Procurement team! Does cost effectiveness say anything to you? Do you want to be the key person in the local supply of services for production sites and/or projects? Do you want to be the interface between sourcing and the stakeholders on site, assuring the right service level? ensure compliance to the group commodity strategies/established group contracts as well as to the defined procurement processes & procedures - Borealis Polymers * Borealis Beringen, Kallo, Zwijndrecht * Contract duration unspecified * Full Time - We don't just make ground-breaking plastics, chemicals and fertilizers. We make discoveries. Our employees are adventurous, eager to explore and lead the way. They are empowered to aim for new opportunities and uncover ground-breaking solutions. Each member of the Borealis team makes a difference, adding value for our customers and society as a whole. Join our dynamic Procurement team! Does cost effectiveness say anything to you? Do you want to be the key person in the local supply of services for production sites and/or projects? Do you want to be the interface between sourcing and the stakeholders on site, assuring the right service level?
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Clinical Data Manager

Brunel Belgium NV

Mechelen

Communication with all involved parties (EDC, STAT, MA, Clinical teams, Client, External Data Providers, Medical Writing, Project Manager Biometrics) … * Preferably, a minimum of 2 years of experience within Clinical Trial Data Management is required. As an experienced CDM you are the Data Management (DM) Lead who is, overall responsible for all the DM activities from the projects on which you are assigned. You are the owner of the clinical SDTM database for your clinical studies and will serve as the Point of Contact towards all involved parties and towards the client. You ensure that trustful, transparent, clean and consistent SDTM data is delivered to the Statistical team at database lock. * Review and testing of the Data Collection Tool (EDC Tool or eSource Tool) * Development of Data Management Plan * Create/review the Data Transfer Agreements with all External Data Providers Communication with all involved parties (EDC, STAT, MA, Clinical teams, Client, External Data Providers, Medical Writing, Project Manager Biometrics) … * Preferably, a minimum of 2 years of experience within Clinical Trial Data Management is required. As an experienced CDM you are the Data Management (DM) Lead who is, overall responsible for all the DM activities from the projects on which you are assigned. You are the owner of the clinical SDTM database for your clinical studies and will serve as the Point of Contact towards all involved parties and towards the client. You ensure that trustful, transparent, clean and consistent SDTM data is delivered to the Statistical team at database lock. * Review and testing of the Data Collection Tool (EDC Tool or eSource Tool) * Development of Data Management Plan * Create/review the Data Transfer Agreements with all External Data Providers
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Data scientist supply chain optimization

VITO

Mol

Mol * Contract duration specified * Full Time - Introduction - You will be member of a team that focuses on supply chain optimization. The team provides supply chain decision support as a service towards public and private clients, via research projects consultancy. To support this activity the team developed MooV, our proprietary linear programming optimization model. More on: MooV. Your responsibilities - As operations research developer you will extend, improve and apply MooV in . * You translate client supply chain optimization requirements into mathematical logics. * You program these logics into the MooV model tailoring it to meet the client's requirements. * You test and validate the model's results in relation to the client's requirements. * You report the results in a (non-technical) decision support format. Mol * Contract duration specified * Full Time - Introduction - You will be member of a team that focuses on supply chain optimization. The team provides supply chain decision support as a service towards public and private clients, via research projects consultancy. To support this activity the team developed MooV, our proprietary linear programming optimization model. More on: MooV. Your responsibilities - As operations research developer you will extend, improve and apply MooV in . * You translate client supply chain optimization requirements into mathematical logics. * You program these logics into the MooV model tailoring it to meet the client's requirements. * You test and validate the model's results in relation to the client's requirements. * You report the results in a (non-technical) decision support format.
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LAB TECHNICIAN

HAYS

Flemish Brabant

HAYS is currently looking for a Lab Technician for a client located in Flemish Brabant. The Lab Technician plays a pivotal role in research based drug development within the pharmaceutical industry. The Lab Technician will perform routine instrument maintenance and troubleshooting, develop knowledge of pre-analytical variables affecting clinical laboratory testing and develop knowledge of disease processes and correlation with clinical laboratory data. You will also perform laboratory investigations, testing, documentation, and routine lab system operations. * Flemish Brabant * Contract duration unspecified * Full Time * Laboratory * Chemistry * Bachelor degree in Sciences - Your responsibilities - Due to the recent growth, our client is in need of qualified and focused driven individuals, like yourself. HAYS is currently looking for a Lab Technician for a client located in Flemish Brabant. The Lab Technician plays a pivotal role in research based drug development within the pharmaceutical industry. The Lab Technician will perform routine instrument maintenance and troubleshooting, develop knowledge of pre-analytical variables affecting clinical laboratory testing and develop knowledge of disease processes and correlation with clinical laboratory data. You will also perform laboratory investigations, testing, documentation, and routine lab system operations. * Flemish Brabant * Contract duration unspecified * Full Time * Laboratory * Chemistry * Bachelor degree in Sciences - Your responsibilities - Due to the recent growth, our client is in need of qualified and focused driven individuals, like yourself.
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Medical Writer

SGS Group Belgium

Mechelen

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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Master in Sciences - Clinical Data Manager

SGS Group Belgium

Mechelen

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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Regulatory Affairs Officer

Real Staffing Brussels (International)

Puurs

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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Clinical Project Manager

Real Staffing Brussels (International)

Gent

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Clincal Research Coordinator

SGS Group Belgium

Antwerpen

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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Medical Affairs Associate

SGS Group Belgium

Mechelen

We are currently seeking for a Medical Affairs Associate. * Involved as internal and external contact for medical affairs projects - 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. This can only happen thanks to We are currently seeking for a Medical Affairs Associate. * Involved as internal and external contact for medical affairs projects - 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. This can only happen thanks to
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Administrative Assistant

SGS Group Belgium

Mechelen

We are currently looking for an Administrative Assistant for out EDC Team - The responsibility of the EDC Assistant is to assist the EDC (Electronic Data Capture) department with project related and/or general administrative work. * You're an all-round administrative wonder. You provide administrative support towards the EDC project team and help them out with practical problems and/or questions; * You have obtained a bachelor's degree in Office Management or you are a Management Assistant (medical secretary is a plus) or equivalent through experience; 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 currently looking for an Administrative Assistant for out EDC Team - The responsibility of the EDC Assistant is to assist the EDC (Electronic Data Capture) department with project related and/or general administrative work. * You're an all-round administrative wonder. You provide administrative support towards the EDC project team and help them out with practical problems and/or questions; * You have obtained a bachelor's degree in Office Management or you are a Management Assistant (medical secretary is a plus) or equivalent through experience; 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.
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