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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
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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
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Receptionist Hospitality Officer

Welcome!

Zaventem

As Receptionist/Hospitality Officer you will be combining multiple clients. is THE Hospitality and Travel Label of Securitas. Welcome! * Zaventem * Contract duration unspecified * Full Time - Introduction - Are you looking for a fabulous place to work? A place with a culture of empowerment, a place where teamwork is important and where you will enjoy what your are doing? In that case, your journey starts at Welcome! What will you be doing * Smile. Your smile is our client's business card. * You will prepare visitors' badges up to the booking of meeting rooms, all what you do, you do it with a smile. Also your are not afraid of some administrative tasks. * You take care of the ordering of catering and office supplies. * You will get the chance to discover what you like. Do what you love and do it with love! Your profile - What baggage do you bring? * Excellent communication and interpersonal skills. As Receptionist/Hospitality Officer you will be combining multiple clients. is THE Hospitality and Travel Label of Securitas. Welcome! * Zaventem * Contract duration unspecified * Full Time - Introduction - Are you looking for a fabulous place to work? A place with a culture of empowerment, a place where teamwork is important and where you will enjoy what your are doing? In that case, your journey starts at Welcome! What will you be doing * Smile. Your smile is our client's business card. * You will prepare visitors' badges up to the booking of meeting rooms, all what you do, you do it with a smile. Also your are not afraid of some administrative tasks. * You take care of the ordering of catering and office supplies. * You will get the chance to discover what you like. Do what you love and do it with love! Your profile - What baggage do you bring? * Excellent communication and interpersonal skills.
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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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QA specialist

Brunel Belgium NV

Diegem

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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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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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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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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Head Contract Management

SGS Group Belgium

Mechelen

In the spirit of continued growth and to help improve our business, we are currently seeking for a Head Contract Management. As Head of Contract Management, you will provide leadership and coaching to the Contract management Team, with the aim to ensure effective, professional and highly qualified contract management activities for SGS Clinical Research. and Support, the Global Director Sales and the Head Proposal Development to ensure proper planning and progression of strategic projects, efficient establishment of cross-departmental communication lines and identifications and development of improvement projects related to the contract management department functions. Your task is to ensure consistent management of all contracts. This generally includes oversight of the contract management process, as well as contract negotiations and document management. In the spirit of continued growth and to help improve our business, we are currently seeking for a Head Contract Management. As Head of Contract Management, you will provide leadership and coaching to the Contract management Team, with the aim to ensure effective, professional and highly qualified contract management activities for SGS Clinical Research. and Support, the Global Director Sales and the Head Proposal Development to ensure proper planning and progression of strategic projects, efficient establishment of cross-departmental communication lines and identifications and development of improvement projects related to the contract management department functions. Your task is to ensure consistent management of all contracts. This generally includes oversight of the contract management process, as well as contract negotiations and document management.
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Secure Data Manager

SGS Group Belgium

Mechelen

The Secure Data Manager will be responsible for the transfer of unblinding data from and to the Secure Data Office and the cleaning of unblinding data within the Secure Data Office. The Secure Data Manager also performs the QC of unblinding data, the cleaning of the data in EDC and/or clinical database and the creation/follow-up of edit checks. We have a challenge for a Secure Data Manager - Mechelen - 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,…). These responsibilities encompass the creation of data transfer agreements, data cleaning documentation and the specification of edit checks and listings. The Secure Data Manager will be responsible for the transfer of unblinding data from and to the Secure Data Office and the cleaning of unblinding data within the Secure Data Office. The Secure Data Manager also performs the QC of unblinding data, the cleaning of the data in EDC and/or clinical database and the creation/follow-up of edit checks. We have a challenge for a Secure Data Manager - Mechelen - 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,…). These responsibilities encompass the creation of data transfer agreements, data cleaning documentation and the specification of edit checks and listings.
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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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