Het overzicht van de statistiek van de lonen bij het beroep "QC Scientist in Belgium"

Make your mark for patientsTo strengthen ourGlobal Analytical Operationsdepartment, we are looking for a talented individual to fill the position of:QC Support Scientist :Critical Material SpecialistinBraine l'Alleud.About the roleScope:Manage critical material supplies for analytical laboratories handling NCE, NBE, and/or GT from phase III to the end of the product life cycleNature:Offer expertise on UCB product regulations and provide support for critical materials in NCE, NBE, and/or GT analytical labs (e.g., reference standards, control samples):Facilitate efficient collaboration with QC, development labs, global analytical services, manufacturing, supply chains, QA, CLO, and CMO as needed.What you will do:Develop expertise in UCB product materials and regulations:Independently create or update Critical materials specifications:Evaluate and set expiration for Critical materials independently.:Collaborate with QC, labs, analytical services, manufacturing, and more:Define and implement simple/local change control:Supervise/manage availability and stock for UCB analytical supplies:Coordinate shipment of Critical materials.:Serve as a key user for LIMS std and reagents:Provide product and system training to the team:Update local procedures and instructions as requested:Execute action plans independently based on clear priorities:Contribute to the implementation of a safe working environment.Interested? For this position you'll need the following education, experience and skills:Master's Degree:Expertise in GMP, NCE, NBE, and GT analytical knowledge and Critical materials regulation.:Validate decisions using strong analytical, troubleshooting and problem:solving skills:Manage multiple projects simultaneously:Team:oriented with a transversal approach:Stress:resistant:Fluent in French with a good level of English.Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from youAbout usUCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.Why work with us?At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equitable opportunities to do their best work. We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities Apply on Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Make your mark for patientsTo strengthen ourGlobal Analytical Operationsdepartment, we are looking for a talented individual to fill the position of:SeniorQC Support Scientist :Critical Material SpecialistinBraine l'Alleud.About the roleScope:Manage critical material supplies for analytical laboratories handling NBE, and/or GT from phase III to the end of the product life cycleNature:Offer expertise on UCB product regulations and provide support for critical materials in NBE and/or GT analytical labs (e.g., reference standards, control samples):Facilitate efficient collaboration with QC, development labs, global analytical services, manufacturing, supply chains, QA, CLO, and CMO as needed.What you will do:Provide expertise in NBE and/or GT critical materials for UCB products, regulations, and processes:Establish or revise critical materials specifications and related documents:Evaluate stability and determine expiry of critical materials:Interface with QC, development labs, Corporate analytical services, manufacturing, supply chains, Global Regulatory affairs, CLO, etc.:Define and implement global:level complex change control:Supervise or support climatic chambers, sample storage and flow:Serve as key user for LIMS std and reagents:Contribute to audit preparation and follow:up:Follow up on deviations and conduct root cause analysis:Participate in implementing a safe working environment to meet site safety objectivesInterested? For this position you'll need the following education, experience and skills:Master's Degree:Expertise in GMP, NBE and GT analytical knowledge and Critical materials regulation.:Validate decisions using strong analytical, troubleshooting and problem:solving skills:Manage multiple projects simultaneously:Team:oriented with a transversal approach:Stress:resistant:Fluent in French with a good level of English.Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from youAbout usUCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.Why work with us?At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equitable opportunities to do their best work. We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities Apply on Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Voor één van onze klanten in Vilvoorde, zijn we momenteel op zoek naar een "Interim manager QA/QC". Functie Omschrijving Onze klant is een gerenommeerd chemie bedrijf. Zij bedienen een groeiende markt in voeding, farma, gezondheidsvoeding en technische toepassingen. Ze streven er altijd naar om 'The Clear Solution' te zijn voor hun klanten. Ze spotten en benutten kansen voor hen, en proberen te anticiperen op toekomstige trends. Ze streven een uitstekende kwaliteit en keuze na, en een vlotte levering. Ze zijn wereldwijd aanwezig, zowel qua productie als qua verkoopondersteuning. Wij zoeken een interim manager QA/QC voor hen, voor een periode van minimaal 6 maanden tot 1 jaar. Verantwoordelijkheden QC : Dagelijkse oversight van QC activiteiten Efficiëntie verhogen van QC: Vanuit een value stream mapping van de core-processen labo - productie QC masterplan opstellen Rapporteringssysteem : voor lab resultaten Quick wins implementeren op basis van zijn/haar kennis van Best practices in kwaliteitslabo in food en farma omgeving Coaching en Ondersteuning van QC team lead, zodat die zich verder ontwikkelt in managerial skills Implementatie van de nieuwe lab organisatie (split QC - application) , opzetten van werkorder systeem tussen QC/proces en R&D lab Governance van lab organisatie via Tier processen SPOC voor BU Group Quality Manager Begeleiden van alignering testmethodes in samenspraak met Group Quality manager Begeleiden van de proces verbeteringen Projectondersteuning : QA/QC rol in projecten QA : Begeleiden van Quality and food safety engineer in het traject naar toekomstige QA afdeling: verschuiven van operationele taken naar productie - management van stakeholders Compliance garanderen: wat is impact van wijzigingen voor de plant -opvolging dat implementatie gebeurd Release van producten - Food safety & Food fraude bewaken Document management systeem mee beheren Profil Profiel We zoeken kandidaten met QA/ QC ervaring. Je hebt ervaring met het begeleiden van een team. Je bent een geboren people manager. Je hebt een uitstekende kennis van het Nederlands en Engels Connaissances linguistiques Nederlands : Goed

To face our constant growth, we are currently actively looking for a Laboratory Scientist- Biology You will be requested to work on projects for the characterisation and quality control of BiomoleculesYOUR MISSION You will report to the Technical leader and you will be part of a team of 5/6 people composed of Laboratory Technicians, Analysts and/or ScientistsAccording to the client's projects and your level of expertise, you may be required to ensure different tasks such asPerforming daily laboratory activities related to method application, development, validation and transfero Performing analyses o Processing datao Writing reports and associated supporting documentso Presenting/discussing resultso Validating raw datao Validating experimental results and ensuring protocols are respectedApplying methods for QC and stability studiesCommunicating with clientsTraining team members and others on technical skills if needed Profil You have a scientific background with knowledge of biologics (Antibody, peptide, protein, ADC...)You are have a strong technical expertise in at least two of these following techniques :Surface Plasmon ResonanceCell-based assaysElectrophoresis testing on proteinsLigand binding assays You have working experience in a regulated environment ideally in the pharmaceutical industryYou have good knowledge of :Working with Cell lines and/or proteins using at least one the following techniques: Cytotoxicity testing (Antibody-Dependent Cell-Mediated Cytotoxicity (ADCC), Complement Dependent Cytotoxicity (CDC), ...), Reporter gene assays, Cell death, Proliferation, SDS-PAGE, Western Blot, IEF, ELISA, biacore, octet and protein dosageDevelopment, validation and/or application of analytical methodsPharmaceutical guidancesWorking experience with antibodies or antibody fragments is a plusYou have good communication skills both in French and English (B2 Level) - writing scientific documents, reports, protocols and mails, phone conferences, contacts with clients. Connaissances linguistiques Français : Bon Anglais : Moyen