Budget Jobs in Antwerp Province

Published

1 of 1
1 of 1

Senior Project Manager

SCIENCE TALENTS

Mechelen

The role of the Senior Project Manager is , plan, execute and simultaneously manage different complex projects within given time, cost and quality constraints, and in line with the respective business case * The Senior Project Manager is part of the PMO team and . * Develop best practices and tools for project execution and management in interaction with other project and/or program managers * Project governance and delivery * Facilitate project initiation and scope definition * Define and manage the delivery of the project's objectives, both from an operational and business delivery point of view * Manage the project * Develop and track project plans (scenario based) including project schedule and resource demand, using appropriate tools * Define and manage project success criteria & risks and disseminate them to involved parties throughout the project life cycle. The role of the Senior Project Manager is , plan, execute and simultaneously manage different complex projects within given time, cost and quality constraints, and in line with the respective business case * The Senior Project Manager is part of the PMO team and . * Develop best practices and tools for project execution and management in interaction with other project and/or program managers * Project governance and delivery * Facilitate project initiation and scope definition * Define and manage the delivery of the project's objectives, both from an operational and business delivery point of view * Manage the project * Develop and track project plans (scenario based) including project schedule and resource demand, using appropriate tools * Define and manage project success criteria & risks and disseminate them to involved parties throughout the project life cycle.
Less More

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
Less More

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.
Less More

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.
Less More

Consolidation & Reporting Analyst

Walters People

Sint-Katelijne-Waver

First contact for local reporting analysts regarding monthly closings or reporting systems - A new job as Consolidation & Reporting Analyst has just become available for a leading multinational firm in Sint-Katelijne-Waver. If you have strong analytical skills, feeling with general accounting and you have a communicative mind-set, this job as Consolidation & Reporting Analyst is made for you! * Set up instructions and reporting canvas for the actuals and budget * Review of incoming reporting of different entities * Assist in uniformization of global reporting * Assist in the set-up of the yearly consolidated IFRS annual accountant and yearly reporting Walters People * Sint-Katelijne-Waver * Temporary with possibility of permanence * Full Time * Review of intercompany data * Prepare consolidation bookings * Develop analysis of key financial data * Assist in the set-up of a consolidated cash flow statement First contact for local reporting analysts regarding monthly closings or reporting systems - A new job as Consolidation & Reporting Analyst has just become available for a leading multinational firm in Sint-Katelijne-Waver. If you have strong analytical skills, feeling with general accounting and you have a communicative mind-set, this job as Consolidation & Reporting Analyst is made for you! * Set up instructions and reporting canvas for the actuals and budget * Review of incoming reporting of different entities * Assist in uniformization of global reporting * Assist in the set-up of the yearly consolidated IFRS annual accountant and yearly reporting Walters People * Sint-Katelijne-Waver * Temporary with possibility of permanence * Full Time * Review of intercompany data * Prepare consolidation bookings * Develop analysis of key financial data * Assist in the set-up of a consolidated cash flow statement
Less More

IT Team lead Manufacturing Applications

Experis

Antwerpen

The Manufacturing applications team is responsible for the lifecycle of manufacturing operations related systems. * You lead the team and activities within the manufacturing domain. Example domains: Production planning & scheduling, manufacturing execution systems (MES), warehouse management (WMS), shop floor logistics, quality management, plant maintenance, industrial automation applications, manufacturing KPI business intelligence, etc. You define a solution for a business problem, this together with your team members, and other supporting people or services. You have accountability for the applications in scope. * You lead projects from feasibility study to closure. In your role as team leader you will manage a team consisting of technical and functional people. You show the ability to develop team competences, and coordinate team activities. The Manufacturing applications team is responsible for the lifecycle of manufacturing operations related systems. * You lead the team and activities within the manufacturing domain. Example domains: Production planning & scheduling, manufacturing execution systems (MES), warehouse management (WMS), shop floor logistics, quality management, plant maintenance, industrial automation applications, manufacturing KPI business intelligence, etc. You define a solution for a business problem, this together with your team members, and other supporting people or services. You have accountability for the applications in scope. * You lead projects from feasibility study to closure. In your role as team leader you will manage a team consisting of technical and functional people. You show the ability to develop team competences, and coordinate team activities.
Less More

You might also be interested in these jobs

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
Less More

Business Development Manager Clinical research (Benelux)

SGS Group Belgium

Mechelen

As Business Development Manager you will be responsible for identifying and exploring strategic business development opportunities within the Clinical Research business in order to maximize organization growth. In the spirit of continued growth and to help improve our business, we are currently seeking for a Business Development Manager Clinical Research (Northern Europe). * that with your extensive knowledge of current market evolutions and conditions you will be responsible for the growth of our Clinical research Business with both new and existing customers, with an emphasis on customer satisfaction and repeat business; * You have experience within the fields of Clinical research and CRO business, or other associated, relevant businesses. * that you will further develop and maintain business development databases. As Business Development Manager you will be responsible for identifying and exploring strategic business development opportunities within the Clinical Research business in order to maximize organization growth. In the spirit of continued growth and to help improve our business, we are currently seeking for a Business Development Manager Clinical Research (Northern Europe). * that with your extensive knowledge of current market evolutions and conditions you will be responsible for the growth of our Clinical research Business with both new and existing customers, with an emphasis on customer satisfaction and repeat business; * You have experience within the fields of Clinical research and CRO business, or other associated, relevant businesses. * that you will further develop and maintain business development databases.
Less More

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.
Less More

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.
Less More

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.
Less More

Global Junior Process Development Specialist

SCIENCE TALENTS

Leuven

To lead process development projects & initiatives to meet or exceed current and future business demands, according to agreed timelines and budget. • To continuously scout and identify new ideas / opportunities in the fields of new processes development, aligned with company strategic pillars, working close together with Product Development, Procurement, Brewing & Quality and Engineering. • To understand consumer insights and competitors' strategy, and to integrate this in the frame of our process development initiatives, to ensure the right decisions are taken in the benefit of the company. o Define development/ implementation plan with internal clients, through definition of KPI, multifunctional team, project structure, project steps and responsibilities at global / zone level. * Leuven * Contract duration unspecified * Full Time - Your responsibilities To lead process development projects & initiatives to meet or exceed current and future business demands, according to agreed timelines and budget. • To continuously scout and identify new ideas / opportunities in the fields of new processes development, aligned with company strategic pillars, working close together with Product Development, Procurement, Brewing & Quality and Engineering. • To understand consumer insights and competitors' strategy, and to integrate this in the frame of our process development initiatives, to ensure the right decisions are taken in the benefit of the company. o Define development/ implementation plan with internal clients, through definition of KPI, multifunctional team, project structure, project steps and responsibilities at global / zone level. * Leuven * Contract duration unspecified * Full Time - Your responsibilities
Less More

(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.
Less More

QA release officer

Oxford Global Resources

Geel

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
Less More

CMC Writer

Oxford Global Resources

Wavre

For one of our clients, located in Wavre, we our currently looking for 2 "CMC Writers". The Technical RA manager is responsible for the preparation, authoring and coordination of CMC submissions related to China Compliance remediations program. * Ensure coordination of activities related to CMC submission file preparation, including change control assessment, source documents collection from key contributing discipline (eg GIO,QC, Site Conformance, etc), initiation and management of CMC submission kick-off meeting,file authoring, review and approval. * Experience in CMC authoring of technical file - Oxford Global Resources * Wavre * Contract duration specified * Full Time - Your responsibilities - Job Description - The person will also be required to interact with regulatory and technical contributing disciplines Teams to ensure File content - definition, submission strategy and preparation coordination. For one of our clients, located in Wavre, we our currently looking for 2 "CMC Writers". The Technical RA manager is responsible for the preparation, authoring and coordination of CMC submissions related to China Compliance remediations program. * Ensure coordination of activities related to CMC submission file preparation, including change control assessment, source documents collection from key contributing discipline (eg GIO,QC, Site Conformance, etc), initiation and management of CMC submission kick-off meeting,file authoring, review and approval. * Experience in CMC authoring of technical file - Oxford Global Resources * Wavre * Contract duration specified * Full Time - Your responsibilities - Job Description - The person will also be required to interact with regulatory and technical contributing disciplines Teams to ensure File content - definition, submission strategy and preparation coordination.
Less More

Expert in EU Labeling

Oxford Global Resources

Woluwe-Saint-Lambert

For one of our clients, located in Sint-Lambrechts-Wolluwé, we are currently looking for an "Expert in EU Labeling". As part of Global Labeling, and under the supervision of the EU Labeling Lead, the EU Labeling Senior Specialist is responsible for the labeling of developmental and marketed products registered under EU procedures (MRP/DCP/CP). Oxford Global Resources * Woluwe-Saint-Lambert * Contract duration specified * Full Time - Your responsibilities - Job Description - The purpose of Global Labeling is to drive labeling strategy and ensure high quality and compliant labeling documents which ensures the safe and effective use of products for patients and healthcare providers, globally. This includes collaboration with the cross-functional labeling team to develop and maintain the EU Product Information (including all its Annexes as defined by EU legislation). Responsibilities For one of our clients, located in Sint-Lambrechts-Wolluwé, we are currently looking for an "Expert in EU Labeling". As part of Global Labeling, and under the supervision of the EU Labeling Lead, the EU Labeling Senior Specialist is responsible for the labeling of developmental and marketed products registered under EU procedures (MRP/DCP/CP). Oxford Global Resources * Woluwe-Saint-Lambert * Contract duration specified * Full Time - Your responsibilities - Job Description - The purpose of Global Labeling is to drive labeling strategy and ensure high quality and compliant labeling documents which ensures the safe and effective use of products for patients and healthcare providers, globally. This includes collaboration with the cross-functional labeling team to develop and maintain the EU Product Information (including all its Annexes as defined by EU legislation). Responsibilities
Less More

1 of 1
1 of 1