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4 résultats pour Biotechnologie à Neder Over Heembeek dans un rayon de 30 km
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• Masterdiploma in een wetenschappelijke richting (bio-engineering, farmacie, biochemie, biotechnologie, …)
• Masterdiploma in een wetenschappelijke richting (bio-engineering, farmacie, biochemie, biotechnologie, …)
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Candidature facile
Voeding of Biochemie, Agro- en Biotechnologie, Voedings- en Dieetkunde, Voedingsmiddelentechnologie …) op zak.
Voeding of Biochemie, Agro- en Biotechnologie, Voedings- en Dieetkunde, Voedingsmiddelentechnologie …) op zak.
NOUVEAU
Eurofins Belgium NV * Brussels * Vast contract, onbepaalde tijd * Voltijds - Introduction - Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Your tasks - Job Description
Eurofins Belgium NV * Brussels * Vast contract, onbepaalde tijd * Voltijds - Introduction - Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Your tasks - Job Description
NOUVEAU
Eurofins Belgium * Brussels * Vast contract, onbepaalde tijd * Voltijds - Introduction - Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description
Eurofins Belgium * Brussels * Vast contract, onbepaalde tijd * Voltijds - Introduction - Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description
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Als projectleider staal werk je nauw samen met onze en hoofdwerfleider, en . * Je bent verantwoordelijk voor de opvolging van alle staal gerelateerde werkzaamheden bij de renovatie van het viaduct van Vilvoorde. Ook de conservering van het staal gebeurt in onderaanneming en wordt door jou opgevolgd. * Stadsbader NV * Brussel of Dessel - Solliciteer als één van de eersten - Introductie - The family company Stadsbader was founded in 1946 in Harelbeke. In the meanwhile, the company is directed by third generation Dominique Valcke. The acquisitions of Deckx AO and Deckx EM in Dessel (2009), Van Maercke Prefab in Kluisbergen (2014) and BAM Contractors (2022) were a strong expansion of the specialisation segments and a reinforcement of the market position. Today the group is daily active in about 250 construction sites in Belgian and the neighbouring countries. Functieomschrijving
Als projectleider staal werk je nauw samen met onze en hoofdwerfleider, en . * Je bent verantwoordelijk voor de opvolging van alle staal gerelateerde werkzaamheden bij de renovatie van het viaduct van Vilvoorde. Ook de conservering van het staal gebeurt in onderaanneming en wordt door jou opgevolgd. * Stadsbader NV * Brussel of Dessel - Solliciteer als één van de eersten - Introductie - The family company Stadsbader was founded in 1946 in Harelbeke. In the meanwhile, the company is directed by third generation Dominique Valcke. The acquisitions of Deckx AO and Deckx EM in Dessel (2009), Van Maercke Prefab in Kluisbergen (2014) and BAM Contractors (2022) were a strong expansion of the specialisation segments and a reinforcement of the market position. Today the group is daily active in about 250 construction sites in Belgian and the neighbouring countries. Functieomschrijving
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“Knowledge is Key”, na een aantal opleidingsdagen op het hoofdkantoor vergezel je de lead auditor om je vers opgedane kennis om te zetten in “op het terrein”. Als Auditor bij SGS kies je voor integriteit. Heb jij als (aankomend) auditor ervaring en kennis van Medical Devices Regulation (MDR) en wil jij aan de slag bij 's werelds meest toonaangevende bedrijf voor inspectie en certificeren? De MDR Lead Auditior voert onafhankelijke audits uit tegen de Medical Devices Regulation (MDR), ISO 13485, MDSAP, UK Medical Devices Regulation, in overeenstemming met vastgestelde procedures en beoordelingsplannen. * SGS Group Belgium * Antwerpen * Vast contract, onbepaalde tijd * Voltijds - Bedrijfsomschrijving - Onafhankelijke audits uitvoeren in de medische hulpmiddelen waardeketen in overeenstemming met vastgestelde procedures en goedgekeurde plannen, waarbij een hoog niveau van dienstverlening wordt gehandhaafd.
“Knowledge is Key”, na een aantal opleidingsdagen op het hoofdkantoor vergezel je de lead auditor om je vers opgedane kennis om te zetten in “op het terrein”. Als Auditor bij SGS kies je voor integriteit. Heb jij als (aankomend) auditor ervaring en kennis van Medical Devices Regulation (MDR) en wil jij aan de slag bij 's werelds meest toonaangevende bedrijf voor inspectie en certificeren? De MDR Lead Auditior voert onafhankelijke audits uit tegen de Medical Devices Regulation (MDR), ISO 13485, MDSAP, UK Medical Devices Regulation, in overeenstemming met vastgestelde procedures en beoordelingsplannen. * SGS Group Belgium * Antwerpen * Vast contract, onbepaalde tijd * Voltijds - Bedrijfsomschrijving - Onafhankelijke audits uitvoeren in de medische hulpmiddelen waardeketen in overeenstemming met vastgestelde procedures en goedgekeurde plannen, waarbij een hoog niveau van dienstverlening wordt gehandhaafd.
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Candidature facile
As a QA GMP Compliance Support, you will act as a Person‑in‑Plan (PIP) at a Contract Manufacturing Organization (CMO) in Germany. You will provide on‑site quality oversight of clinical drug product manufacturing activities and ensure compliance with GMP requirements and applicable Quality Agreements. A leading global pharmaceutical organisation, recognised for its high standards in quality, GMP compliance, and patient safety, operating in a highly regulated environment and working closely with external manufacturing partners for the production of pharmaceutical products, including sterile drug products. * Ensure that clinical batches are manufactured in compliance with GMP standards and Quality Agreements - o Performing GEMBA walks when required to ensure process compliance * Escalate critical quality issues and support impact assessments in collaboration with the
As a QA GMP Compliance Support, you will act as a Person‑in‑Plan (PIP) at a Contract Manufacturing Organization (CMO) in Germany. You will provide on‑site quality oversight of clinical drug product manufacturing activities and ensure compliance with GMP requirements and applicable Quality Agreements. A leading global pharmaceutical organisation, recognised for its high standards in quality, GMP compliance, and patient safety, operating in a highly regulated environment and working closely with external manufacturing partners for the production of pharmaceutical products, including sterile drug products. * Ensure that clinical batches are manufactured in compliance with GMP standards and Quality Agreements - o Performing GEMBA walks when required to ensure process compliance * Escalate critical quality issues and support impact assessments in collaboration with the
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Experienced Auditor with 2 to 3 years sought for international firm. * Sander Brussels * Bruxelles * Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - Diverse projects, strong training, clear growth path and competitive package. Do you have 2 to 3 years of experience in audit and want to grow within an international and ambitious environment? We are partnering with a leading audit and advisory firm with a strong global presence, currently strengthening its Belgian teams. Role - As part of a structured audit team, you will work on diverse assignments under the supervision of . • Performing audit procedures across different cycles • Collecting and analysing financial and operational data • Preparing audit working papers and reports • Reviewing the accuracy and completeness of financial statements • Identifying internal control weaknesses and proposing improvements
Experienced Auditor with 2 to 3 years sought for international firm. * Sander Brussels * Bruxelles * Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - Diverse projects, strong training, clear growth path and competitive package. Do you have 2 to 3 years of experience in audit and want to grow within an international and ambitious environment? We are partnering with a leading audit and advisory firm with a strong global presence, currently strengthening its Belgian teams. Role - As part of a structured audit team, you will work on diverse assignments under the supervision of . • Performing audit procedures across different cycles • Collecting and analysing financial and operational data • Preparing audit working papers and reports • Reviewing the accuracy and completeness of financial statements • Identifying internal control weaknesses and proposing improvements
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Candidature facile
Progressive is voor het OOSTERWEELPROJECT op zoek naar een Civil Project Engineer. Als Civil Project Engineer draag je rechtstreeks bij aan één van de meest uitdagende infrastructuurprojecten van ons land: de Oosterweelverbinding. Ben jij geïnteresseerd in de rol van Civil Project Engineer? * Je hebt Masterdiploma in Bouwkunde / Civil Engineering of je bent gelijkwaardig door ervaring * PROGRESSIVE * Antwerpen * Freelance * Voltijds - Solliciteer als één van de eersten - Snel solliciteren - Het Oosterweelproject, ook wel gekend als de "werf van de eeuw" is één van de meest complexe en grootschalige infrastructuurprojecten die Vlaanderen ooit heeft gekend. Jouw verantwoordelijkheden * In deze functie vorm je de brug tussen ontwerp en uitvoering. Je bekijkt elk onderdeel door een technische bril, beoordeelt wat mogelijk is op het terrein en werkt oplossingen uit die het werk vlot en veilig houden.
Progressive is voor het OOSTERWEELPROJECT op zoek naar een Civil Project Engineer. Als Civil Project Engineer draag je rechtstreeks bij aan één van de meest uitdagende infrastructuurprojecten van ons land: de Oosterweelverbinding. Ben jij geïnteresseerd in de rol van Civil Project Engineer? * Je hebt Masterdiploma in Bouwkunde / Civil Engineering of je bent gelijkwaardig door ervaring * PROGRESSIVE * Antwerpen * Freelance * Voltijds - Solliciteer als één van de eersten - Snel solliciteren - Het Oosterweelproject, ook wel gekend als de "werf van de eeuw" is één van de meest complexe en grootschalige infrastructuurprojecten die Vlaanderen ooit heeft gekend. Jouw verantwoordelijkheden * In deze functie vorm je de brug tussen ontwerp en uitvoering. Je bekijkt elk onderdeel door een technische bril, beoordeelt wat mogelijk is op het terrein en werkt oplossingen uit die het werk vlot en veilig houden.
Candidature facile
We are recruiting a Regulatory Affairs Manager to join a well‑established, family‑owned pharmaceutical SME with a strong presence in the BELUX and NL markets. * Solid experience in Regulatory Affairs (medior-senior level) within the pharmaceutical industry - The organization operates in a stable SME environment, combining fast decision‑making with high regulatory and quality standards. You will be responsible for the regulatory management of a diverse pharmaceutical portfolio (OTC & Rx, generics, multiple dosage forms), covering national, MRP and DCP procedures (no centralized procedures). * Defining and advising on regulatory strategy for new and existing products * Managing regulatory submissions (new MAs, variations, renewals) in eCTD format * Providing scientific and technical regulatory expertise, including Module 3 compliance * Monitoring regulatory changes and advising accordingly
We are recruiting a Regulatory Affairs Manager to join a well‑established, family‑owned pharmaceutical SME with a strong presence in the BELUX and NL markets. * Solid experience in Regulatory Affairs (medior-senior level) within the pharmaceutical industry - The organization operates in a stable SME environment, combining fast decision‑making with high regulatory and quality standards. You will be responsible for the regulatory management of a diverse pharmaceutical portfolio (OTC & Rx, generics, multiple dosage forms), covering national, MRP and DCP procedures (no centralized procedures). * Defining and advising on regulatory strategy for new and existing products * Managing regulatory submissions (new MAs, variations, renewals) in eCTD format * Providing scientific and technical regulatory expertise, including Module 3 compliance * Monitoring regulatory changes and advising accordingly