QA & Ra Set-up Specialist

**Our mission** UgenTec is an international and fast-growing bio-IT company specialized in the development of diagnostic & workflow software for molecular laboratories. The UgenTec software solutions are situated on the challenging crossroad between IT, data science and biotechnology. We’re on a mission to heavily disrupt the rules in our market and are...

QA Specialist | Liège | FR - EN | CDI Notre client, une biotech ayant son siège dans la province de Liège, est activement à la recherche d'un(e) **QA Specialist** ayant au moins deux ans d'expérience dans une fonction QA généraliste. En tant que **QA Spécialist**, vous contribuerez au développement et à la maintenance du Système de Gestion de la...

AMP?AMP (bpost group) est la plus grande société de distribution de presse en Belgique. A partir de 5 sites de distribution et de bureaux en Flandre, à Bruxelles et en Wallonie, nous desservons 5.000 points de vente de presse et distribuons 425.000 magazines et 260.000 journaux par jour. Aujourd'hui, nous renforçons encore notre position en...

AMP?AMP (bpost group) est la plus grande société de distribution de presse en Belgique. A partir de 5 sites de distribution et de bureaux en Flandre, à Bruxelles et en Wallonie, nous desservons 5.000 points de vente de presse et distribuons 425.000 magazines et 260.000 journaux par jour. Aujourd'hui, nous renforçons encore notre position en...

**The validator of innovative technologies** You want to make use of your medical expertise? - CIP, CIR, CEP, CER, PMS, PMCF, PSUR_ ring a bell for you? Do you agree that the matter lies in the details or beyond the details? Then you cannot miss this job ad! **Who we are?** COVARTIM is an engineering company located in Brussels. Our mission is to help...

Heb jij een Master afgerond binnen de Life Sciences of Farmacie en wil jij binnen Quality Assurance uiteindelijk graag doorgroeien tot back-up Qualified Person (QP), of heb je dit certificaat al? Lees dan snel verder! Voor een werkgever die toelevert aan de sector Life Sciences (pharma) te regio Brussel, ben ik namelijk op zoek naar een QA Officer. **LOTUS...

Catalent Pharma Solutions is the leading global provider of advanced delivery technologies and development solutions for drugs, biologics and consumer health products. With over 80 years serving the industry, Catalent has proven expertise in providing development, production and packaging services for pharmaceutical and biotech companies. For our sterile...

Liege | QA Officer | FR - EN | CDI **Notre client** ***Notre client est une biotech active dans la province de Liège. Dans le cadre d’une réorganisation interne, le département QA a été remodelée afin d’y ajouter un poste medior. Ils sont donc actuellement à la recherche d’une personne ayant au moins 2 années d’expérience dans une fonction...

**What can you expect?**: Our Software Testers have been breaking new ground in **Quality Assurance in an Agile/ DevOps environment**. If you want to be part of this amazing team, keep reading. Because we are looking for a **QA Specialist** to strengthen our team and build the best solutions for our customers. **What will do you as a QA Specialist?** °...

**Super-hero working for the compliance of medical devices** - ISO 13485, 21 CFR, 510(k), MDR 2017/745, IVDR 2017/746_ mean more than a series of numbers and letters for you? Working on several projects in parallel does not scare you? But, on the contrary, you are looking for a varied job? Knowing that your job can have an impact on people's health gets you...

Shyfter is not just another SaaS startup; we are on a mission to dominate the HR-Tech industry. Our innovative platform is transforming the HR sector, offering a suite of powerful apps that redefine how businesses manage their human resources and workforce operations. From our inception, we've set the pace for growth—tripling our size each year —and...

**Function**: Supervisor Global QA Systems Reporting to Director Global QA Systems **Purpose**: As Supervisor you lead a group of QA systems officers and assistants. You coordinate and check all global activities in the area of Quality Assurance and compliance and conduct all responsibilities and rights as defined in regulations to ensure an optimal...

**Overview**: QA Expert Quality System & Compliance **Responsibilities**: Be the QA Expert Quality System & Compliance for Mithra Pharmaceuticals SA, Novalon SA, Estetra SRL, Neuralis SA and Mithra R&D SA. Be responsible for maintaining and improving the QMS of Mithra Group. Drive and maintain an appropriate level of compliance to Mithra Group QMS. Drive...

Brussels, BE **Our Company**: CordenPharma is a leading Contract Development & Manufacturing (CDMO) partner with approximately 2’000 employees across Europe and the United States and annual revenues > 500 M€, enabling pharmaceutical and biotechnology companies to link their requirements for product success with their patients’ healthier...

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Local Start Up Specialist II (LSUS) to join our A-team (hybrid*/remote)! The Local Start-up Specialist (LSUS) coordinates and...

As part of this function, the QA System & Compliance Expert will provide support during internal audits, customer audits and regulatory inspections, as well as during new product introduction projects.Additionally, the QA System & Compliance Expert will act as back-up for other routine activities of the QA System & Compliance department (e.g. change control...

**Een superheld die zich inzet voor de conformiteit van medische hulpmiddelen** Betekenen ISO 13485, 21 CFR, 510(k), MDR 2017/745, IVDR 2017/746 voor jou meer dan een reeks cijfers en letters? Schrikt het parallel werken aan verschillende projecten je niet af? Maar ben je juist op zoek naar een afwisselende baan? Als je weet dat jouw job een impact kan...

**Superheld die zich inzet voor de conformiteit van medische hulpmiddelen** Betekenen ISO 13485, 21 CFR, 510(k), MDR 2017/745, IVDR 2017/746 voor jou meer dan een reeks cijfers en letters? Schrikt het parallel werken aan verschillende projecten je niet af? Maar ben je juist op zoek naar een afwisselende baan? Als je weet dat jouw job een impact kan hebben...

**De beoordeler van innovatieve technologieën** Wil je je medische expertise inzetten? Zeggen CIP, CIR, CEP, CER, PMS, PMCF, PSUR je iets? Ben je het ermee eens dat het hem in de details zit? Dan mag je deze vacature niet missen! **Wie zijn wij?** COVARTIM is een ingenieursbureau gevestigd in Brussel. Onze missie is om de MedTech-industrie te helpen...

The Senior Regulatory Affairs Manager (RAM) has as primary task to take care of the several Regulatory Affairs (RA) activities of the RA-QA-PV Unit. For the Reg Affairs Manager this means the life cycle management of a group of product registrations of MSD AH Benelux. This life cycle management involves translation of product information texts and taking...