Metrics Jobs in Flemish Brabant

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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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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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Quality Assurance & Nutrition Regulatory Affairs Assistant

Nutrition & Santé BeNeLux

Vilvoorde

To assist N&S management in all Safety, Quality and Regulatory areas related to N&S brands, products and product related material in line with the company objectives and together with all involved departments (QA & NRA sister's organizations, Marketing, Business Support Management, Sales) * Supporting digital communication regarding regulatory & quality issues (social media) for all N&S brands * Previous experience in regulatory affairs is a plus Nutrition & Santé BeNeLux * Support regulatory requests for information by: the submission for registrations of NUT numbers in the national database (only for Belgium) * Analyzing, drafting and establishing internal regulatory policies and training them out to internal QA/NRA staff. * Studying towards a Food Science, Nutrition or law related degree * Vilvoorde * Apprenticeship * Full Time - Purpose - Key Responsibilities To assist N&S management in all Safety, Quality and Regulatory areas related to N&S brands, products and product related material in line with the company objectives and together with all involved departments (QA & NRA sister's organizations, Marketing, Business Support Management, Sales) * Supporting digital communication regarding regulatory & quality issues (social media) for all N&S brands * Previous experience in regulatory affairs is a plus Nutrition & Santé BeNeLux * Support regulatory requests for information by: the submission for registrations of NUT numbers in the national database (only for Belgium) * Analyzing, drafting and establishing internal regulatory policies and training them out to internal QA/NRA staff. * Studying towards a Food Science, Nutrition or law related degree * Vilvoorde * Apprenticeship * Full Time - Purpose - Key Responsibilities
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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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Sr. Regulatory Affairs Specialist EMEA - Food Supplements

Nu Skin Belgium

Zaventem

Train regulatory specialists and other Nu Skin departments (Marketing/Legal/Quality/…) on regulatory requirements - In this role you will take on Sr. responsibilities in the Regulatory Affairs team and . * +- 5 years in Product Regulatory Affairs for food supplements or food at EU level * On-time filing of regulatory submissions and post-approval maintenance of regulatory dossiers. Ensure product regulatory compliance for food supplements and food with national and EU regulations including composition, claims, labeling and product registration/notification requirements. * Interact with project teams and regulatory agencies in relation to submissions and other relevant topics. * Develop a regulatory strategy for issues which could significantly impact project timelines and costs. * Provide direction in the New Product Development process as regulatory lead Train regulatory specialists and other Nu Skin departments (Marketing/Legal/Quality/…) on regulatory requirements - In this role you will take on Sr. responsibilities in the Regulatory Affairs team and . * +- 5 years in Product Regulatory Affairs for food supplements or food at EU level * On-time filing of regulatory submissions and post-approval maintenance of regulatory dossiers. Ensure product regulatory compliance for food supplements and food with national and EU regulations including composition, claims, labeling and product registration/notification requirements. * Interact with project teams and regulatory agencies in relation to submissions and other relevant topics. * Develop a regulatory strategy for issues which could significantly impact project timelines and costs. * Provide direction in the New Product Development process as regulatory lead
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Global Sensory & Consumer Science Manager

Modis Belgium

Leuven

Interested to join our Life Sciences team as a Global Sensory & Consumer Science Manager? You want to be part of an international company that brings together the best experts in the field of Life Sciences, IT and engineering? MODIS is an international company that brings together the best experts in the field of Life Sciences, IT and engineering. As part of the Global Sensory and Consumer science group, you will shape and align Sensory and Consumer learning plans related to commercial or technical platform to ensure successful innovation launches to be implemented in 6 geographical Zones (North America, Middle America, South America, Europe, Africa and Asia Pacific). * Lead Sensory & Consumer science capabilities development as well as related best practices task forces across functions and zones. * Supervise and influence external PhD and Post docs related to Sensory & Consumer science fields. Interested to join our Life Sciences team as a Global Sensory & Consumer Science Manager? You want to be part of an international company that brings together the best experts in the field of Life Sciences, IT and engineering? MODIS is an international company that brings together the best experts in the field of Life Sciences, IT and engineering. As part of the Global Sensory and Consumer science group, you will shape and align Sensory and Consumer learning plans related to commercial or technical platform to ensure successful innovation launches to be implemented in 6 geographical Zones (North America, Middle America, South America, Europe, Africa and Asia Pacific). * Lead Sensory & Consumer science capabilities development as well as related best practices task forces across functions and zones. * Supervise and influence external PhD and Post docs related to Sensory & Consumer science fields.
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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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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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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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Inhouse CRA

VALESTA NV

Diegem

As an Inhouse CRA you play a crucial part in the smooth conduct of the Clinical Research process. * Do you have a first experience with clinical trials and are you ambitious to become a CRA? * Ensures both regulatory and clinical protocol compliance is maintained for all assigned clinical projects. * In consultation with the assigned field clinical and appropriate in-house personnel, coordinates the start-up and maintenance of the clinical study site. * Serves as a liaison to clinical study management, field clinical personnel and site personnel by responding to any protocol-related issues and escalating as appropriate. * Ensures the clinical study site adheres to the assigned protocol and all applicable regulatory standards. * Trains internal and external clinical professionals to ensure compliance with established protocols. * Minimum 2 years of clinical experience As an Inhouse CRA you play a crucial part in the smooth conduct of the Clinical Research process. * Do you have a first experience with clinical trials and are you ambitious to become a CRA? * Ensures both regulatory and clinical protocol compliance is maintained for all assigned clinical projects. * In consultation with the assigned field clinical and appropriate in-house personnel, coordinates the start-up and maintenance of the clinical study site. * Serves as a liaison to clinical study management, field clinical personnel and site personnel by responding to any protocol-related issues and escalating as appropriate. * Ensures the clinical study site adheres to the assigned protocol and all applicable regulatory standards. * Trains internal and external clinical professionals to ensure compliance with established protocols. * Minimum 2 years of clinical experience
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