Protocols Jobs in Antwerp Province

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SUPPORT IN PHARM TECH OPS ACTIVITIES

HAYS

Putte

You will also track the status of new and ongoing changes, coordinate the activities (planning, execution, finalization) together with internal (validation, production, planning, quality, laboratories, …) and external (global support functions, suppliers, …) parties. Writing, executing protocols to support these changes and writing, updating procedures or work instructions within the scope of the activities will also be part of the job. * Putte * Freelance * Full Time - HAYS is currently looking for a Expert in Pharmaceutical Processes, Validation and Project management. Temporary position of 1 year in a Pharmaceutical company located near Putte (Mechelen) Your responsibilities * Pharma Technical Operations * Freelancer or Contractor * Pharma sector, mission of 1 year You will also track the status of new and ongoing changes, coordinate the activities (planning, execution, finalization) together with internal (validation, production, planning, quality, laboratories, …) and external (global support functions, suppliers, …) parties. Writing, executing protocols to support these changes and writing, updating procedures or work instructions within the scope of the activities will also be part of the job. * Putte * Freelance * Full Time - HAYS is currently looking for a Expert in Pharmaceutical Processes, Validation and Project management. Temporary position of 1 year in a Pharmaceutical company located near Putte (Mechelen) Your responsibilities * Pharma Technical Operations * Freelancer or Contractor * Pharma sector, mission of 1 year
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Electrical ASIC Engineer Medical

VeroTech

Mechelen

To reinforce our Electronics team, VeroTech is looking for a Electrical ASIC Engineer Medical! As an Electrical ASIC Engineer Medical you are responsible for the verification and validation of new ASICs for medical devices. You work in a team with other ASIC electrical engineers and in . VeroTech manages and develops R&D engineers & projects. * Define electrical concepts to verify the requirements * Develop and verify ASIC Verification Environment (FPGA) * Minimum 3 years of experience in Electrical Engineering * Experience in digital ASIC design and/or FPGA - VeroTech * Mechelen * Contract duration unspecified * Full Time - Introduction - VeroTech ( ), is a young, dynamic and fast growing company specialized in consultancy and engineering services for R&D projects. Clients are multinationals and large companies in sectors such as telecom, automotive, transportation, semiconductor and medical, ... To reinforce our Electronics team, VeroTech is looking for a Electrical ASIC Engineer Medical! As an Electrical ASIC Engineer Medical you are responsible for the verification and validation of new ASICs for medical devices. You work in a team with other ASIC electrical engineers and in . VeroTech manages and develops R&D engineers & projects. * Define electrical concepts to verify the requirements * Develop and verify ASIC Verification Environment (FPGA) * Minimum 3 years of experience in Electrical Engineering * Experience in digital ASIC design and/or FPGA - VeroTech * Mechelen * Contract duration unspecified * Full Time - Introduction - VeroTech ( ), is a young, dynamic and fast growing company specialized in consultancy and engineering services for R&D projects. Clients are multinationals and large companies in sectors such as telecom, automotive, transportation, semiconductor and medical, ...
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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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Senior Application Support Engineer

Experis

Antwerp

5+ years of IT experience preferably as a system administrator or software engineer or as an operational/product support engineer in a dynamic 24x7 environment. * Developing and enhancing scripts to support the product line. * Providing level 1 and level 2 supports for all customer related issues reported and escalated by global customer support adhering to current established SLAs. * Working with both offshore and onshore teams in all aspects of operations, release management and product support. * Participating in a 7x24 rotating support operations * Experienced in supporting and troubleshooting applications and related issues. (3+ years). * Experienced with administration/configuration of Java, Apache, and Tomcat applications. * Understanding of multi-tiered web application architecture. * Knowledge of WebSphere MQ, WebSphere Application Server and Elastic Search is a plus 5+ years of IT experience preferably as a system administrator or software engineer or as an operational/product support engineer in a dynamic 24x7 environment. * Developing and enhancing scripts to support the product line. * Providing level 1 and level 2 supports for all customer related issues reported and escalated by global customer support adhering to current established SLAs. * Working with both offshore and onshore teams in all aspects of operations, release management and product support. * Participating in a 7x24 rotating support operations * Experienced in supporting and troubleshooting applications and related issues. (3+ years). * Experienced with administration/configuration of Java, Apache, and Tomcat applications. * Understanding of multi-tiered web application architecture. * Knowledge of WebSphere MQ, WebSphere Application Server and Elastic Search is a plus
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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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(Senior) Clinical Data Manager (CDM)

SGS Group Belgium

Mechelen

In the spirit of continued growth and to help improve our business, we are currently seeking for a (Senior) Clinical Data Manager (CDM). * Communication with all involved parties (EDC, STAT, MA, Clinical teams, Client, External Data Providers, Medical Writing, Project Manager Biometrics) … As an experienced CDM you are the Data Management the (Data Management) (DM) Lead who is, overall responsible for all the DM activities from the projects on which you are assigned. * Preferably, a minimum of 2 years of experience within Clinical Trial Data Management is required. 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. In the spirit of continued growth and to help improve our business, we are currently seeking for a (Senior) Clinical Data Manager (CDM). * Communication with all involved parties (EDC, STAT, MA, Clinical teams, Client, External Data Providers, Medical Writing, Project Manager Biometrics) … As an experienced CDM you are the Data Management the (Data Management) (DM) Lead who is, overall responsible for all the DM activities from the projects on which you are assigned. * Preferably, a minimum of 2 years of experience within Clinical Trial Data Management is required. 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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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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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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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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Electrical ASIC Engineer Medical

VeroTech

Mechelen

To reinforce our Electronics team, VeroTech is looking for an Electrical ASIC Engineer Medical! As an Electrical ASIC Engineer Medical you are responsible for the verification and validation of new ASICs for medical devices. You work in a team with other ASIC electrical engineers and in . VeroTech manages and develops R&D engineers & projects. * Define electrical concepts to verify the requirements * Develop and verify ASIC Verification Environment (FPGA) * Minimum 3 years of experience in Electrical Engineering * Experience in digital ASIC design and/or FPGA - VeroTech * Mechelen * Contract duration unspecified * Full Time - Introduction - VeroTech, is a young, dynamic and fast growing company specialized in consultancy and engineering services for R&D projects. Clients are multinationals and large companies in sectors such as telecom, automotive, transportation, semiconductor and medical, ... To reinforce our Electronics team, VeroTech is looking for an Electrical ASIC Engineer Medical! As an Electrical ASIC Engineer Medical you are responsible for the verification and validation of new ASICs for medical devices. You work in a team with other ASIC electrical engineers and in . VeroTech manages and develops R&D engineers & projects. * Define electrical concepts to verify the requirements * Develop and verify ASIC Verification Environment (FPGA) * Minimum 3 years of experience in Electrical Engineering * Experience in digital ASIC design and/or FPGA - VeroTech * Mechelen * Contract duration unspecified * Full Time - Introduction - VeroTech, is a young, dynamic and fast growing company specialized in consultancy and engineering services for R&D projects. Clients are multinationals and large companies in sectors such as telecom, automotive, transportation, semiconductor and medical, ...
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