Quality Control Jobs in Flemish Brabant

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Logistics Coordinator

PPD

Zaventem

Responsible for logistics coordination of low to moderately complex studies. Ensures all logistics aspects are considered for Sponsors/CRO and Site Services. * Previous experience in logistics is preferred. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development to deliver life-changing therapies that improve health. Main contact person between Project management, vendors and sites. Responsible for logistics coordination of low to moderately complex studies. Ensures all logistics aspects are considered for Sponsors/CRO and Site Services. * Previous experience in logistics is preferred. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development to deliver life-changing therapies that improve health. Main contact person between Project management, vendors and sites.
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Lead Medical Technologist

PPD

Zaventem

Leads the day-to-day operations of the laboratory unit. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development to deliver life-changing therapies that improve health. Performs analysis and evaluates individual and related laboratory data, recognizes patterns or trends that suggest significance of results and determines the level of clinical significance. Leads the day-to-day operations of the laboratory unit. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development to deliver life-changing therapies that improve health. Performs analysis and evaluates individual and related laboratory data, recognizes patterns or trends that suggest significance of results and determines the level of clinical significance.
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QA/QC Engineer

Parkwind NV

Leuven, Oostende

To reinforce our QHSSE team, we are looking for a QA/QC Engineer. As part of the QA/QC team, you will contribute to the company and departmental goals by upholding the highest quality standards possible during the construction of our wind farm projects, as well as the maintenance afterwards. * Draft Employer Requirements (QA/QC) * Develop and implement a QA Plan, Quality processes and procedures * Attend (where necessary) internal (team) meetings that include QA topics - Parkwind NV * Leuven, Oostende * Contract duration unspecified * Full Time - Parkwind NV is a leading company in Europe in the field of developing, building and running offshore wind farms. The Parkwind team was instrumental in the development, financing, construction and operational maintenance of Belwind I (a 165+6 MW plant) as well as Northwind (a 216 MW plant) and Nobelwind (a 165 MW plant). To reinforce our QHSSE team, we are looking for a QA/QC Engineer. As part of the QA/QC team, you will contribute to the company and departmental goals by upholding the highest quality standards possible during the construction of our wind farm projects, as well as the maintenance afterwards. * Draft Employer Requirements (QA/QC) * Develop and implement a QA Plan, Quality processes and procedures * Attend (where necessary) internal (team) meetings that include QA topics - Parkwind NV * Leuven, Oostende * Contract duration unspecified * Full Time - Parkwind NV is a leading company in Europe in the field of developing, building and running offshore wind farms. The Parkwind team was instrumental in the development, financing, construction and operational maintenance of Belwind I (a 165+6 MW plant) as well as Northwind (a 216 MW plant) and Nobelwind (a 165 MW plant).
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QA COMPLIANCE SPECIALIST PHARMACEUTICAL DISTRIBUTION

HAYS

Huizingen

For this position of QA Specialist, your primary role is to support efficient distribution of high quality products in compliance to regulatory and customer requirements. As Quality and compliance specialist, you will support the operational activities in performing risk analyses, investigate issues, handle deviations and advice on corrective and preventive actions (CAPAs). As QA specialist, you will participate in the implementation of the Quality Systems needed in the warehousing and distribution activities. For this QA specialist role, we are looking for someone with a scientific background (master pharmacist, bio-engineer, … Hays Life Sciences is currently looking for a Quality Specialist (QA and compliance) for a huge international player in the distribution of pharmaceutical products. * Quality Assurance and Compliance for distribution activities * Huizingen * Contract duration unspecified For this position of QA Specialist, your primary role is to support efficient distribution of high quality products in compliance to regulatory and customer requirements. As Quality and compliance specialist, you will support the operational activities in performing risk analyses, investigate issues, handle deviations and advice on corrective and preventive actions (CAPAs). As QA specialist, you will participate in the implementation of the Quality Systems needed in the warehousing and distribution activities. For this QA specialist role, we are looking for someone with a scientific background (master pharmacist, bio-engineer, … Hays Life Sciences is currently looking for a Quality Specialist (QA and compliance) for a huge international player in the distribution of pharmaceutical products. * Quality Assurance and Compliance for distribution activities * Huizingen * Contract duration unspecified
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Senior Quality Engineer

Pall Life Sciences

Hoegaarden

The Senior Quality Engineer is leading quality investigation, keeping oversight of quality complaints (internal and external) and managing the metrics and KPI (Q OBEYA) related to this. The Senior Quality Engineer will be closely engaged in R&D projects towards introduction of new products as quality lead. The senior quality engineer is maintaining the overview of the validated state of products, processes, methods and equipment. The Senior Quality Engineer is in plant wide projects. * Support Supplier Quality Engineer for related issues (SCARs), work closely with Purchasing / SS to select/maintain/drop Suppliers list based on their performance; Our QUALITY DEPARTMENT in Hoegaarden is looking forward to welcoming an * Support transfer from NPI to high volume manufacturing and develop quality control plans; The Senior Quality Engineer is leading quality investigation, keeping oversight of quality complaints (internal and external) and managing the metrics and KPI (Q OBEYA) related to this. The Senior Quality Engineer will be closely engaged in R&D projects towards introduction of new products as quality lead. The senior quality engineer is maintaining the overview of the validated state of products, processes, methods and equipment. The Senior Quality Engineer is in plant wide projects. * Support Supplier Quality Engineer for related issues (SCARs), work closely with Purchasing / SS to select/maintain/drop Suppliers list based on their performance; Our QUALITY DEPARTMENT in Hoegaarden is looking forward to welcoming an * Support transfer from NPI to high volume manufacturing and develop quality control plans;
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Assistant, Investigator Central Labs

PPD

Zaventem

Under general supervision, the Assistant, Investigator Central Labs sites, monitors, and other departments within Global Central Labs through communication of information, training sites and documentation of services pertaining to clinical trials. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development to deliver life-changing therapies that improve health. Under general supervision, the Assistant, Investigator Central Labs sites, monitors, and other departments within Global Central Labs through communication of information, training sites and documentation of services pertaining to clinical trials. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development to deliver life-changing therapies that improve health.
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Software Test Engineer

VeroTech

Ghent

To reinforce our Software Engineering team, VeroTech is looking for a Software Test Engineer. As Software Test Engineer, you are responsible for the development of a test plan for different kind of products (e.g. digital signatures, smart card technologies etc). VeroTech manages and develops R&D engineers & projects. * Analyse the requirements and set-up test cases * Perform the functional tests according to the test plan * Select and maintain the best tools and automate the test environment * Document and report test results * Minimum a few years of experience with functional testing within software development * Good understanding of the software lifecylcle * Experience with writing test plans and testing of web, mobile and native applications - VeroTech * Ghent * Contract duration unspecified * Full Time - Introduction To reinforce our Software Engineering team, VeroTech is looking for a Software Test Engineer. As Software Test Engineer, you are responsible for the development of a test plan for different kind of products (e.g. digital signatures, smart card technologies etc). VeroTech manages and develops R&D engineers & projects. * Analyse the requirements and set-up test cases * Perform the functional tests according to the test plan * Select and maintain the best tools and automate the test environment * Document and report test results * Minimum a few years of experience with functional testing within software development * Good understanding of the software lifecylcle * Experience with writing test plans and testing of web, mobile and native applications - VeroTech * Ghent * Contract duration unspecified * Full Time - Introduction
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Master in (Biomedical) Science (Clinical Data Manager)

SGS Group Belgium

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 Science Services 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 have obtained a Master's Degree in a paramedical area or biomedical sciences. SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Introduction - At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice. 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 Science Services 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 have obtained a Master's Degree in a paramedical area or biomedical sciences. SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Introduction - At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice.
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SERVICE TECHNICIAN FOR THE PHARMA INDUSTRY - 50K !

ARBALETT

Namur

Service technician – Function Service technician– Profile Service technician – Offer * You will intervene in the frame of the after-sale service * Namur * Contract duration unspecified * Full Time - Introduction - Our client, world leader in the field of high-end equipment for the pharmaceutical and biotech industries, is looking for new talents to join its growing team ! You are trustworthy, meticulous, autonomous and flexible? You want to acquire good technical skills in the pharmaceutical sector and grow in the company in the long run? Then this opportunity suits you! Your tasks * You are in charge of on-site installation of highly sophisticated equipment (Isolator Systems) in Benelux and the North of France * You are responsible to execute, control the commissioning, qualification and test protocols of isolators on our customer's sites. Your profile Service technician – Function Service technician– Profile Service technician – Offer * You will intervene in the frame of the after-sale service * Namur * Contract duration unspecified * Full Time - Introduction - Our client, world leader in the field of high-end equipment for the pharmaceutical and biotech industries, is looking for new talents to join its growing team ! You are trustworthy, meticulous, autonomous and flexible? You want to acquire good technical skills in the pharmaceutical sector and grow in the company in the long run? Then this opportunity suits you! Your tasks * You are in charge of on-site installation of highly sophisticated equipment (Isolator Systems) in Benelux and the North of France * You are responsible to execute, control the commissioning, qualification and test protocols of isolators on our customer's sites. Your profile
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Customer Service & Logistics Manager F/M

Essity

Diegem

University degree or min. of 4 years equivalent job experience in Customer Service or Logistics Join a great team that is eager to learn and want to excel in customer service. * Develop and implement customer service indicators in order to assure excellence in customer service. Passionate about delivering high quality services to clients? * Liaise with functional or operational area managers (for example sales, marketing, finance, supply) to align all business needs. * Help to secure service levels at the lowest distribution cost. * Strong customer- and result oriented - Essity * Diegem * Contract duration unspecified * Full Time - Essity is a leading global hygiene and health company dedicated to improving well-being through products and solutions, essentials for everyday life. The name Essity stems from the words essentials and necessities. Our sustainable business model creates value for people and nature. University degree or min. of 4 years equivalent job experience in Customer Service or Logistics Join a great team that is eager to learn and want to excel in customer service. * Develop and implement customer service indicators in order to assure excellence in customer service. Passionate about delivering high quality services to clients? * Liaise with functional or operational area managers (for example sales, marketing, finance, supply) to align all business needs. * Help to secure service levels at the lowest distribution cost. * Strong customer- and result oriented - Essity * Diegem * Contract duration unspecified * Full Time - Essity is a leading global hygiene and health company dedicated to improving well-being through products and solutions, essentials for everyday life. The name Essity stems from the words essentials and necessities. Our sustainable business model creates value for people and nature.
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Medical affairs associate

Ausy Group Belgium NV

Kampenhout

As a Medical Affairs Associate, RIP) in the review and approval of promotional activities and materials for multiple pharmaceutical companies in Benelux and contribute in pharmacovigilance projects. IN2Pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects to pharmaceutical and healthcare industry in Benelux. They are looking to expand the team with a Medical Affairs colleague who has the ambition and potential to grow in our organization. * Experience in other domains: medical writing, Regulatory Affairs or Pharmacovigilance - Ausy Group Belgium NV * Kampenhout * Contract duration unspecified * Full Time - Take a look here! Our offices are located at “Hof ter Loonst” in Kampenhout. As a Medical Affairs Associate, RIP) in the review and approval of promotional activities and materials for multiple pharmaceutical companies in Benelux and contribute in pharmacovigilance projects. IN2Pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects to pharmaceutical and healthcare industry in Benelux. They are looking to expand the team with a Medical Affairs colleague who has the ambition and potential to grow in our organization. * Experience in other domains: medical writing, Regulatory Affairs or Pharmacovigilance - Ausy Group Belgium NV * Kampenhout * Contract duration unspecified * Full Time - Take a look here! Our offices are located at “Hof ter Loonst” in Kampenhout.
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VeroTech

Leuven

As Project Manager Medical Devices, you take ownership of different electronic design projects from beginning to end for product development projects, with a focus on the medical devices industry. To reinforce our Electronics team, VeroTech is looking for a Project Manager Medical Devices. 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, ... VeroTech manages and develops R&D engineers & projects. * Execute on a daily base the project according to the project plan and manage the milestones * Report about and monitor the whole project * At least 10 years of experience in project management * Experience with medical industry and with certification procedures are an advantage As Project Manager Medical Devices, you take ownership of different electronic design projects from beginning to end for product development projects, with a focus on the medical devices industry. To reinforce our Electronics team, VeroTech is looking for a Project Manager Medical Devices. 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, ... VeroTech manages and develops R&D engineers & projects. * Execute on a daily base the project according to the project plan and manage the milestones * Report about and monitor the whole project * At least 10 years of experience in project management * Experience with medical industry and with certification procedures are an advantage
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Diegem

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International Sales Specialist

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Python Developer Medical

VeroTech

Mechelen

As Python Developer Medical, you play a key role in the development and implementation of a Python verification framework and toolboxes used in the medical industry for ASIC verification. To reinforce our Software team, VeroTech is looking for a Python Developer Medical * Translate requirements into object-oriented Python software design * Implement and review the Python code and verification scripts * Professional experience in object-oriented software development (Python) 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, ... As Python Developer Medical, you play a key role in the development and implementation of a Python verification framework and toolboxes used in the medical industry for ASIC verification. To reinforce our Software team, VeroTech is looking for a Python Developer Medical * Translate requirements into object-oriented Python software design * Implement and review the Python code and verification scripts * Professional experience in object-oriented software development (Python) 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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