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

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

1 200 € Gemiddeld maandsalaris

Niveau van het gemiddelde loon tijdens de laatste 12 maanden: "QA in Belgium"

Valuta: EUR USD Jaar: 2021
Op de staafdiagram is de verandering van het gimiddelde loon van het beroep QA in Belgium getoond.

Indeling van de "QA" vacatures in de regionen Belgium

Valuta: EUR
Volgens het diagraam zijn er in Belgium het grootste aantal vakatures van de beroep QA in geopend. Op de tweede plaats staat {regionPName2} en op de derde {regionPName3}.

Top provincies Belgium volgens niveau van het loon voor de beroep "QA"

Valuta: EUR
Volgens het diagraam zijn er in Belgium het grootste aantal vakatures van de beroep QA in geopend. Op de tweede plaats staat {regionPName2} en op de derde {regionPName3}.

Top van de gelijkaardige vacatures volgens niveau van het loon in Belgium

Valuta: EUR
Onder de gelijkaardige beroepen in Belgium met het meest hoge loon is JavaScript-ontwikkelaar. Volgens de gegevens van onze site het niveau van het loon bedraagt 2847 eur. Op de tweede plaats staat Dynamics Ax-consultant met het loon van 2300 eur en op de derde plaats staat HTML-ontwikkelaar met het loon van 2267 eur.

Aanbevolen vacatures

QA CUSTOMER & COMPLIANCE LEAD (H/F/X) (h/f)
Actiris,
Based in Gosselies, the mission of Catalent Cell and Gene Therapy is to deliver optimized process industrialization capacities to cell therapy organizations and speed up the arrival of their therapies onto the market. From technology selection to business modelling, through GMP manufacturing, process development, quality services, Catalent's teams are fully committed to helping their clients fulfil their objective of providing sustainable and affordable therapies to their patients.To lead its increasing number of development and manufacturing projects, Catalent Cell and Gene Therapy is looking for a motivated QA Customers & Compliance Lead. The RoleThe QA Customers & Compliance Lead reports to the QA Customer & Compliance Manager and is responsible to:In relation with specific QA customer & compliance activities:Be a Subject Matter Expert covering QA questions related to project initiation QA activities, by customers or internal teams.Be the interface between the QA department and all other Catalent departments and customer for QA aspects related to projects he/she is leading.Warn/ report periodically the QA Customer & Compliance manager in case of issue.Ensure for the project he/she is leading the QA documentation review against regulatory files, current regulations and customer requests.Ensure QA Readiness of the project he/she is leading at every steps.¿Follow customer related deviations, OOS, change control, risk assessments, CAPA, complaint.Ensure Batch Disposition¿ of the project in collaboration with the QA Customer & Compliance Manager.To ensure to have the appropriate training before performing an activity and updates QA training related to his/her activity.Ensure customers expectation are fulfilled.Communicate and to interact effectively with the colleagues of QA department for QA aspects related to projects he/she is leading (e.g. for initial manufacturers/suppliers/ subcontractors' approval, for equipment management lent by customers, for document review, etc.).Participate to Quality Agreement establishment with customers¿.The QA Customer & Compliance Lead is the back-up of the QA Customer & Compliance Manager for project launch aspects. In relation with CTLT values and performance:Vehicle Catalent values, QA department vision and mission.Ensure a Patient First Culture.Implement pertinent tools of operational excellence Lean culture.Implement and follow-up Key Performance Indicators. He/she proposes and takes appropriate actions.Feed and support initiatives in Environment Health and Safety protecting life and well being Transversal and/or regulatory activities:Maintain an open and effective communication with all other departments.Take part to audits when necessary.Follow competent authorities and customers audit¿s and the related CAPA plan.Contact regulatory agency.Participate and ensure regulatory monitoring.Perform self-inspections The CandidateQualifications & SkillsAt least Master degree or higher in Sciences and relevant experience in cell and gene therapy.Experience of minimum 5 years in quality assurance is required.Efficient communicator and willing to bring new challenges.Demonstrated leadership and cross functional team spirit.Rigorous, conscientious, organized, versatile, open-minded & quality-minded.Ability to multi-task and demonstrate diplomatic and leadership skills.Customer oriented.Demonstrates initiative and ability to meet deadlines.Ability to effectively present information and respond to questions from management and customers.Fluency in French: good speaking, reading and writing skills.Good reading comprehension and writing skills in English.Computer skills: Microsoft office, ETQ, ComplianceWire, TrackWise are a plus.Knowledge of existing and emerging social media technologies and channels a plus.  Catalent's standard leadership competencies that are used to interview and for Perf Profil - Connaissances linguistiques Français : Bon Anglais : Moyen
QA Support Master Documents & Artwork Review at Ausy
Ausy, Antwerp, HEIST-OP-DEN-BERG
Heb jij ervaring met document review binnen de farma? Dan is deze QA vacature zeker iets voor jou!Deze farmaspeler in Heist-op-den-Berg is op zoek naar een QA Support Master Documents & Artwork Review die tijdelijk het team komt versterken. Ben jij reeds vertrouwd met QA binnen de farma dan mag je jouw CV doorsturen naar laurence.teerlynck@cx.ausy.be of bel naar 03 369 19 80.Als QA Support Master Documents & Artwork Review sta je in voor het opmaken, aanmaken en goedkeuren van master documenten.Zo maak je certificaten op voor herwerking en registratie doeleindenReview en approval van Bill of Materials (BOM) en Artwork behoort tot jouw takenpakketVerder ben je ad hoc support voor het ISO Quality teamFunctie-eisenWetenschappelijke BachelorJe kan goed overweg met het MS Office pakket (Word, Excel, ...)Administratief sta je sterk in je schoenenWerkervaring binnen een GMP-omgeving heb je ook op zakTalenkennis: NL + ENGArbeidsvoorwaardenJe bent flexibel ingesteld en hiervoor krijg je veel terug. Je krijgt onder meer een aantrekkelijk salarispakket aangevuld met extralegale voordelen en een vast contract of projectcontract op basis van jouw interesses en mogelijkheden. Wat betekent dit concreet bij AUSY?een brutoloon o.b.v. jouw ervaringen,groepsverzekering,hospitalisatieverzekering,maaltijdcheques van 7€/dag,13e maandrepresentatiekosten van 50€ netto/maand (full time),terugbetaalde dienstverplaatsing of firmawagen,Daarnaast bieden wij ook tal van opleidingen, fun-activiteiten, doorgroeimogelijkheden, ... om je doorheen je carrière te begeleiden.
QA Compliance Officer Process Reviewer QC & utilities at Real Staffing
Real Staffing, Antwerp, Geel
QA operations QC & utilities, expertise HVAC / utilities is closely linked to technical services (TS), contamination control, quality control & validation. The department is responsible for guaranteeing the quality of the production process with a special focus on TS activities and ensuring that this is in line with the prescribed procedures, standards, business practices and legislation. Responsibilities Follow up, review & handle TS related issues (quality events, CAPAs, changes) so that they are completed compliant Follow up, review & handle environmental excursions (EEX) so that they are concluded compliant Review of trend reports, alarms, risk assessments, procedures,… with regard to EM & utilities Reading and interpreting documentation regarding current and new compliance standards and regulatory trends and actions Participate in internal & external audits and inspections Involvement in any QA and interdepartmental project initiatives Support with problem solving meetings regarding TS / contamination control related topics In possession of a Master in a scientific direction, or equivalent through experience Experience within Pharma and Quality Feeling with HVAC utilities, is able to work with quality systems, experience writing deviations, ... Experience PHENIX Basic knowledge and interpretation of cGLP / cGMP / cGCPs in a regulated environment Outstanding accuracy and attention to detail Independence and a strong sense of responsibility Interpersonal skills, an enthusiastic team player Good writing skills Good knowledge of the Dutch and English language
QA PROJECT MANAGER - Ardo Group
Ardo, Ardooie, Flanders
De uitdaging Profile Positive, enthusiastic personality with a healthy dose of ambition Job requirements You have a Master's degree in a scientific direction, preferably as a bio- or industrial engineer. You have at least 5 years of relevant work experience in a quality function, in the food processing industry or FMCG is a plus but not a must. You have experience with ERP and a strong affinity with software applications and tools in quality. Experience in QMS is nice to have, but not a necessity. You speak English fluently (French and or Dutch is a plus). Competencies Initiator, result-oriented Organizer with helicopter view and strong sense of responsibility Relationship builder and team player Facilitator, inspiring personality Smooth communicator Jouw talent Do you have a soft spot for quality and sustainability and would you like to put this into practice? Do you want to help build a strong vision on quality and food safety from the field to the consumer? Would you like to put this on the map across borders in Europe? Bringing healthy food to the end consumer just feels good. Being able to do this within the industry's leading company is an added bonus, isn't it? Function Centralization of the knowledge of quality You work from the Group Quality team in a matrix structure where you support the 21 local QA teams in 9 countries on a project basis with the standardization and centralization of quality processes. You analyze the current workflows, work out improvement proposals and know how to convert these into implementation via action plans. You work from the Ardo Group vision on quality and sustainability in order to achieve a single standard across the various sites, taking into account local and group needs. You support the integration of quality within the ERP system and you work closely with the international key users community. You are part of the multidisciplinary working group in which you identify quality integration points together with your colleagues Project Managers from other departments (including Purchase, Sales, Supply Chain, Finance, Master Data,…) to obtain smooth end-to-end processes. You can communicate excellently and at different levels in the company, both with your own team and internationally and cross company. You report to the Group Quality Director. Ons aanbod Ardo Group Ardo has 4000 employees and has 21 production sites in 9 countries. The family business sells in more than 100 countries and has a turnover of more than 1.1 billion euros. Ardo's mission is to preserve nature's gift as pure as possible. Ardo achieves this goal thanks to an integrated network of growing areas, production units, freezing units, packaging equipment, appropriate logistics and thorough quality control. It is Ardo's ambition to be a worldwide champion in the field of sustainable fresh-frozen plant-based foods by focusing on innovation and sustainability, by inspiring people and by contributing to a healthier lifestyle. These ambitions have been translated into our MIMOSA program, which stands for Minimum Impact & Maximum Output Sustainable Agriculture. Location Ardooie, occasional 10% travel in Europe, plus home office flexibility Offer A dynamic working environment and close-knit family corporate culture within an international company with a strong future-oriented sustainability strategy and vision. A varied job with responsibility in quality in the broadest sense, in which you make a direct impact on the business on a daily basis through improvements and in which you can spar with your colleagues from other countries. A job in an essential economy (food business). A permanent contract with a competitive salary package, supplemented with a company car and other benefits. Are you interested? Please then apply via www.ceresrecruitment.be . For more information, please contact Nathalie Platevoet, who can be reached by telephone on +32 (0) 483 596798 . Detailed information about the company can be found at www.ardo.com. Ardo has outsourced the recruitment and selection for the vacancy QA Project Manager exclusively to CeresRecruitment.
QA Engineer
Synergie Klein Brabant Careers, PUURS-SINT-AMANDS
Onze klant is als onafhankelijk, Belgisch familiebedrijf reeds actief sinds 1986 in de farmaceutische industrie. Zo zijn ze uitgegroeid tot dé partner bij uitstek voor de top 20 farma bedrijven in België. Vanop hun 2 sites in Puurs staan ze met onze 200 enthousiaste en gedreven medewerkers elke dag klaar om het veelzijdig aanbod aan niet-steriele geneesmiddelen te produceren en te verpakken. Ook verlenen ze diensten op vlak van onderzoek en ontwikkeling. Het familiale karakter zit in hun DNA. Daarom hechten ze veel belang aan de waarden betrouwbaarheid, collegialiteit en engagement.Taken: Opvolgen van incidenten en deviaties, impact analyse doen en root cause onderzoek waar nodig. Verantwoordelijk zijn voor de behandeling, opvolging en rapportering van klachten. Doen van de jaarlijkse evaluatie van elk farmaceutisch product en je bent mee verantwoordelijk voor het opvolgen van de kwalificatie van leveranciers. Instaan voor de verdere uitbouw van ons kwaliteitssysteem volgens de GMP in nauwe samenwerking met de QA supervisor aan wie je rechtstreeks rapporteert. Zeer actief meewerken/meedenken aan het opstellen en implementeren van procedures in het algemeen en in het bijzonder procedures met betrekking tot validatie, kalibratie en training. Geven van algemene trainingen zoals GMP-trainingen, lijnfasen binnen productie en verpakking, … Je neemt actief deel aan het aansturen, uitwerken en het opvolgen van projecten omtrent kwaliteitsverbetering van producten, processen en diensten binnen Purna.Wat zoeken we? Bachelor/Master diploma in een wetenschappelijke richting (Chemie, Farmaceutische wetenschappen,...) Een enthousiaste en professionele teamspeler die in staat is om het kwaliteitsbeleid over te dragen aan alle collega's. Initiatief nemen, zeer georganiseerd werken met een sterke mate van autonomie en engagement voor het bedrijf. Verbindende communicatieve vaardigheden met een uitstekende kennis van het Engels, zowel mondeling als schriftelijk. Je werkt voornamelijk in dagdienst maar kan indien nodig in 2-ploegen werken.Wat bieden we?Je maakt deel uit van een groeiende organisatie en je komt terecht bij ervaren professionals die elkaar enthousiast ondersteunen. Als team werken we constructief samen aan hetzelfde doel, in een open positieve sfeer, met respect voor elkaar, strevend naar een fijne, motiverende, inspirerende werkomgeving. Tegelijkertijd krijg je de kans om op een onafhankelijke manier te werken, waarbij je het vertrouwen krijgt om prioriteiten te stellen.Betrokkenheid, verantwoordelijkheid nemen, initiatief en continue verbetering zijn diep verankerd in onze bedrijfscultuur met daarnaast een competitief salarispakket.
QA Controller Alcon
Synergie Alcon Interim, Puurs
Heb jij ervaring in Quality Control en wil jij graag deel uitmaken van Alcon? Aarzel dan niet en solliciteer vandaag nog op onderstaande vacature!Takenpakket:Je staat in voor inkomende inspectie. De QA controller voert nauwkeurig en met oog voor detail de inspecties van binnenkomende componenten uit volgens de geldende procedures.Bijkomende testen en staalnames ook uitvoeren volgens het vastgelegde jaarlijks programma.In geval van componenten die geradieerd dienen te worden of dienen herverpakt te worden door externen, zal de coördinatie van deze activiteiten ook door jou gebeuren.Ook de controle van de DHR en afsluiten/ingeven van het werkorder; controle en vrijqave van prototypes , incl. steriele prototypes vallen onder jouw takenpakket.Wat zoeken we? Ervaring in Qa/ inspectie Diploma secundair onderwijs (ASO/TSO) Zeer goede kennis van Nederlands en Engels PC vaardigheid Profiel: Nauwkeurig, vlot, enthousiast, graag in team werken (doelen worden niet persoonlijk behaald maar via team), na opleiding vrij zelfstandig kunnen werken, bereid zijn om in drie ploegen te werken (vroeg/laat/nacht).Wat bieden we?Marktconform loon aangevuld met extralegale voordelenHoogtechnologische werkomgevingTewerkstelling op lange termijn (met kans op een vast contract)
QA Officer (H/F)
PaHRtners, Liège (Ville) (BE)
San’Up est une société en pleine croissance active dans la phytothérapie, les compléments alimentaires et l’homéopathie. L’entreprise est reconnue pour la qualité de ses produits qu’elle commercialise à l’international. La société, active en région liégeoise, dévoile des projets de développement ambitieux. Son site de production (environnement GMP) connait une phase de développement importante. L’équipe professionnelle et dynamique de San’Up a pour mission de contribuer à l’amélioration de la qualité de vie de nombreuses personnes à travers le monde. Pour plus d’information concernant l’entreprise, ses valeurs et sa vision, contactez recruitment@pahrtners.be.   Dans ce contexte de croissance, San’Up souhaite renforcer son équipe Qualité. Nous sommes dès lors activement à la recherche d’un(e) (h/f) : QA Officer.   Responsabilités : En tant que QA Officer, vous participez au bon fonctionnement du système de gestion de la qualité relatif aux activités de production. Vous contribuez au respect des normes GMP et GDP.  Les responsabilités suivantes vous sont confiées :  Participer et implémenter la stratégie qualité de l’entreprise. Etablir, documenter et maintenir à jour le système de gestion de la qualité (QMS).  Participer à la préparation des audits internes et externes : clients, fournisseurs et autorités. Contribuer à la libération des lots après analyse des dossiers de fabrication et d’analyse. Prendre en main les non conformités et implémenter les actions rectificatrices. Rédiger les procédures des activités de validation et qualification des équipements. Réaliser les revues annuelles de lots et mener des programmes d’amélioration continue.  Rapporter régulièrement l’évolution des activités vers le management. Profil :  Vous êtes titulaire d’un Master à orientation scientifique, ou équivalent par expérience.  Vous disposez d’une première expérience en QA dans l’industrie pharma/biotech.  Vous possédez une bonne connaissance des GMP. Une expérience avec la FDA est un atout.  Vous êtes rigoureux/se, méthodique, autonome, et disposez d’un bel esprit d’équipe. Vous avez une bonne capacité organisationnelle et communicationnelle. Vous avez une bonne connaissance du français. Une bonne maîtrise de l’anglais est un atout. Vous appréciez prendre des décisions et faites montre d’une capacité à fédérer les équipes.  Vous démontrez une belle envie de délivrer un travail de qualité, en équipe. Offre :  Une fonction diversifiée incluant des responsabilités et des projets intéressants.  Des défis professionnels, scientifiques et humains enrichissants. Des possibilités de développement et d’évolution stimulantes. Intégrer une structure industrielle conviviale et en pleine croissance.  Un salaire attractif reprenant des avantages extra-légaux, en ligne avec votre expérience.  Intéressé(e) ?  Envoyez votre CV accompagné d'une courte lettre de motivation via https://www.pahrtners.be/fr/offres-demploi/qa-officer-hf/ ou à : recruitment@pahrtners.be.  Votre candidature sera traitée en toute confidentialité. 
QA Automation Engineer
Dover Fueling Solutions, Grobbendonk, Flanders
As a QA and Automation Engineer you will work within a highly skilled development team. You will integrate and develop test automation tools for testing our Point-of-Sale solution. You are or will ... De vacatureAs a QA and Automation Engineer you will work within a highly skilled development team. You will integrate and develop test automation tools for testing our Point-of-Sale solution. You are or will become a specialist in test automation and seek continuously to optimize QA in the development process. Next to working on test automation you are aware that manual testing is also important for delivering the best solutions possible to our customers in an environment where quality and time-to-market are crucial. Therefore, you are open to take up your responsibility and help the team with manual tests.Functie eisenYou have a software engineering background (preferable C# knowledge)Selenium is more for you than a chemical elementYou know that Jira and qTest are working together seamlesslyYou always see opportunities to automate everyday tasks You are eager to learn about our productsYou are a QA automation specialistYou feel proud and responsible for what you deliverYou have a strong analytical mindset and can define test paths based on functional specifications, user stories or customer requirementsWe are a global company, so the English language does not have any secrets for youJouw belangrijkste taken1. You will integrate and develop test automation tools for testing our Point-of-Sale solution2. Vacature QA Automation Engineer | Cooder.be3. Optimize QA in the development process4. Manual testing5. Gedeeltelijk vanuit huisOver Dover Fueling SolutionsTokheim is one of the world’s leading manufacturers of fuel dispensing and automation equipment. With manufacturing centres and network of distributors in many countries around the globe, Tokheim offers customers a complete range of fuel dispensers and pumps, retail automation systems, payment terminals, media devices, replacement parts and upgrade kits. Tokheim has over 2,000 employees and is an operating company within Dover Fueling Solutions and the Dover Corporation.Tokheim remains a company committed to meeting the needs of customers around the globe. We pride ourselves in being able to meet the entire fuel dispensing needs of customers, whatever size or type of service stations they own, wherever in the world they operate.Opgericht in 18901 kantoor1000+ medewerkers36 is de gemiddelde leeftijdWat kan je?DevelopmentBachelor, Master denkniveauMedior werkniveauNederlands sprekendWat krijg je?Vast€ 2300 - € 4500 bruto per maandGlijdende werkurenLease autoTankkaartMobielLaptop13e maandPensioenNetto onkostenvergoedingWat doe je?Minimaal een 38-urige werkweekSamenwerken met 0-10 collega'sJe werkt samen metSales, IT, Klantenservice, HRFocus opB2BJe werkt voornamelijk met Informatietechnologie en -diensten
QA/QC ENGINEER
CTI Education Group, Brussel, Brussel Hoofdstad, Bruxelles
Job Description - QA/QC ENGINEER (NUC00000771) Job Description QA/QC ENGINEER [ NUC00000771 ] Tractebel is a global community of 5000 imaginative experts engineering a carbon-neutral future. Through our game-changing solutions for complex energy, urban, nuclear and water projects, we help our clients create a positive impact towards a sustainable world, where people, planet and profit collectively thrive. Work environment The Mechanical Equipment Department is in charge of the following tasks : expertise in mechanical components and related Codes & Standards; procurement and qualification of mechanical Equipment and Nuclear Fuel; quality Surveillance and manufacturing follow-up; management of repair and replacement activities; in service Inspection and Ageing Management; fuel Quality Control and Handling. Mission As a member of the “QA/QC” section you will ensure that Tractebel’s suppliers deliver and install their products with the highest level of quality to ensure nuclear safety at all times. You will have the opportunity to be involved in the full supply chain in a practical and industrial environment and this in an international setting. You will be mainly in charge of the following activities in collaboration with other sections within the mechanical department, and in close relation with the Contract Owner and the Customers. You are autonomous in the examination and approval of the Contractor technical manufacturing and installation files of various mechanical equipment (valves, pumps, heat exchangers, piping, …) for the nuclear fleet in Belgium and in an international context. As such you are experienced in the review and approval of material purchase specifications, non-destructive examination procedures, heat treatment procedures, special manufacturing procedures, You have an experience with ASME Boiler and Pressure Vessel Code Section III or RCCM or have at least a knowledge of the methodology of other code and standards for pressure equipment. Act as lead quality control engineer for one or multiple projects depending on the project scale where you will be the single point of contact for our internal and external clients requesting advice on quality related matter including quality issues, treatment of non-conformities and derogation requests. Knowledge of materials and their fabrication processes is a must. Conduct quality control missions during manufacturing and installation of mechanical equipment in an international context. You will assess the conformity of the fabrication during inspection missions at manufacturer's premises and/or during installation at the Nuclear Power Plants of Doel and/or Tihange. You will verify that the goods are meeting the requirements set forth in the technical and upfront approved technical and quality assurance documentation. You have experience in destructive and non-destructive testing of materials and welded structures. You are familiar with quality control aspects and methods, quality plans, fabrication procedures, non-destructive examination techniques, end of manufacturing records, material certificates, surface treatments, … Issue inspection reports following the templates of Tractebel. You will inform the contract owner or report directly to the project manager of the outcome of your missions. Qualifications Profile Mechanical Engineer or equivalent by experience in quality control of mechanical equipment; French or Dutch speaking with a professional knowledge of the English language; Able to work with limited supervision according to predefined methodologies; A strong interest in manufacturing processes of mechanical equipment for nuclear power plants; Ability to draft concise reports containing factual conclusions; Knowledge of quality control, fabrication processes, non-destructive testing, material technology & standards and manufacturing; Reliable and motivated to meet deadlines; Knowledge of the nuclear industry is a plus; Eager to work in an international context for short or long term inspection missions; Interested to perform quality control inspections on the site of Doel or Tihange Nuclear Power Plant located in Belgium; Flexible regarding time-schedule; resistant to stress .
QA / Automation Engineer - Silicon Valley - Brussels(remote) Nigel Frank International
Expat Network, Antwerpen
Expat Network | Supporting expats for more than 30 years This organization specializes in making the lives of people better. First, they created an amazing product that revolutionized the driving experience for millions of drivers globally. Now, they are launching a new product which is a global services platform that aims at bringing together likeminded people who share the same passions. So, if you want to be part of something new, something great and something lucrative, this is your chance. Soft Skills Requirements Being a good cultural fit is more important than being a good technical fit, that's why the Soft Skills are above the Hard Skills here. As you'll be part of an international team with a strong work ethic, you're expected to have the virtues of grit, integrity, and respect. You're also motivated, eager to improve yourself and help your team become better too with your creative mind and your energetic mentality. You need to be a passionate person who genuinely wants to be part of something new with a great potential. Technical Requirements You have relevant experience with Test Automation frameworks like Appium, Selenium, or WebDriver. We're looking for experience in mobile testing . You can run and automate mobile UI tests on emulators and real devices. You know about CI/CD pipelines. Your coding skills in scripting and automation are of sufficient quality. Nice Bonus Points Knowledge of microservices, web technologies, back-end architectures, and cloud infrastructure (AWS). Salary, Benefits & Allowances In addition to the opportunity to join an international team of specialists that manage to maintain a start-up mentality in their modern office, you may also expect an agile and flat company culture, full of growth opportunities, free coffee, and lots of food. Also, the following: Yearly gross salary range from €55000 for Mid-level up to, approximately, €70000 for Senior level. On top of this salary, you get the following: Monthly representation allowance of €150 - €250 net. Mobility allowance or a company car, whatever you choose. 26 paid holidays plus the extra ADV holidays (10/year) that come on top of these 26 days offered by the company. Monthly phone subscription. Health & Group Insurance. A 30% bonus on your annual gross salary and company stock options. Remote Work - You are supposed to visit the office 2-3 days per month. Application Process Reach out to me, George Christofakakis for a guaranteed interview with the hiring managers. I'll help you build a strong application and go all the way to the end and the employment offer. There are some questions provided by the company that need to be answered as part of the screening process that will determine whether or not you'll be invited. Write to my email at g.christofakakisjeffersonfrank.com Only registered members can apply for jobs. 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QA/QC Manager
Metagenics, Oostende
Fill out the online application or e-mail your CV and cover letter to HR (talentmetagenics.eu). Your application will be handled with strict confidentiality. Stay up to date by signing up to our newsletter
QA / QC ENGINEER
OFFRE D'UNE AUTRE REGION, Hamont-Achel, Maaseik
Geactualiseerd op 08 maart 2021via OFFRE D'UNE AUTRE REGION Jouw uitdaging: In deze functie word je de rechterhand van de Quality Manager en maak je deel uit van het Quality team met collega¿s in België en in Polen. Je werkt nauw samen met je collega¿s binnen Quality. Maar je hebt ook veel bredere contacten in de organisatie: je overlegt met R&D, Productie, Sales¿. Jij wordt binnen de organisatie de trekker voor alles wat met QA te maken heeft: je zorgt ervoor dat de procedures en kwaliteitssystemen optimaal geïmplementeerd worden. Zo zorg je er pro-actief voor dat alle producten conform de kwaliteitseisen van de band rollen. En draag jij je steentje bij aan de groei van dit warme bedrijf. Je krijgt de verantwoordelijkheid om klachten van klanten (die rechtstreeks binnenkomen, of via Sales) te analyseren en onderzoeken. Daartoe doe je ¿ in samenspraak met de Quality Manager en je QC collega de nodige testen en analyses. Je neemt elke klacht serieus en bezorgt de klant een gefundeerd antwoord. Want elke klacht biedt je de mogelijkheid om dingen weer anders en beter te doen. Op basis van je analyses en doorgedreven testing kom je met een onderbouwd rapport en advies: voor productie, voor R&D, voor logistiek¿ Maar daar stopt het natuurlijk niet: op basis van je verbeteradviezen zullen er weer nieuwe verbeterprojecten moeten worden opgestart in de betrokken afdelingen. Je overlegt dan ook nauw met je QC collega en met de mensen op de vloer. Op die manier krijg je helder hoe de controles gebeuren en de systemen ingesteld zijn. En wat er beter kan. Je formuleert voorstellen tot correctieve acties en je bekijkt samen met QC en de manager van de betrokken afdeling hoe je de juiste controlesystemen best op de vloer geïmplementeerd krijgt. Je zorgt voor de input voor heldere en duidelijke werkinstructies. Het is dan ook belangrijk dat je heel regelmatig op de vloer vinger aan de pols houdt en dat je vlot contacten legt met heel wat verschillende mensen in het bedrijf. Spaas is ook een bedrijf dat, samen met zijn klanten, sterk wil inzetten op duurzaamheid. De wetgeving (REACH, CLP, Product Safety¿) en certificeringen hierrond (denk aan ISO 9001:2015, BRC CP¿) worden hoe langer hoe belangrijker en strikter. Het zal ook jouw taak zijn om deze regelgeving continu op te volgen. En te bekijken hoe je dit in de interne organisatie moet vertalen, want hier komen natuurlijk nieuwe verbeterprojecten uit voort. Ook hier is het belangrijk dat je je advies helder rapporteert en grondig overlegt met de betrokken afdelingen. Je neemt ook je verantwoordelijkheid voor een stuk Quality administratie: elk kwaliteitssysteem staat of valt met de correcte en up-to-date procedures en instructies. Het updaten en herzien van procedures zal dan ook een deel van je taak zijn. Daarnaast kan het ook voorkomen dat je betrokken wordt bij administratieve projecten rond regelgeving. Zo zorg je bijvoorbeeld voor correcte UK REACH registraties (heel actueel na de Brexit). Waar nodig leg je ook contact met federaties en externe instanties die je meer informatie kunnen bezorgen. Zo groeit jouw kennis en kun je deze ook weer doorgeven in het bedrijf. Op termijn zul je ook mee audits in goede banen leiden. Kortom een mooie en veelzijdige QA functie waar je in kennis enorm zult groeien en kunt rekenen op een fijne samenwerking met een enthousiaste Quality Manager die graag haar kennis met je deelt. En heel wat uitdagende projecten, vandaag en in de toekomst. Je hebt een master in biowetenschappen of gelijk(w)aardig. Je hebt minimaal al een paar jaar werkervaring in een QC en/of QA functie in een productiebedrijf. Je bent communicatief sterk. Je hebt een analytische geest en werkt nauwkeurig; je gaat tot aan het gaatje. Je hebt een basiskennis van chemie en chemische processen. Je hebt een creatieve en probleemoplossende spirit. Je bent sterk in het planmatig en projectmatig werken. Je Nederlands en Engels zijn vlot (mondeling en schriftelijk). Je bent een echte teamspeler Talenkennis Beheer van ondernemingen en diensten / Beheer van diensten Naam van de werkgever Presentatiewijze een motivatiebrief en een C.V. te versturen via e-mail Opgelet Het is niet nodig om Actiris te contacteren voor deze werkaanbieding. De vacature werd opgesteld door de werkgever. Actiris is niet verantwoordelijk voor de inhoud ervan en eventuele inbreuken tegen de wetgeving. Toch een opmerking over deze werkaanbieding? Aarzel dan niet om Actiris in te lichten.
QA/QC Project Engineer
OneJob, Arendonk, Turnhout
Vanaf de start van het project maak je deel uit van het projectteam en je analyseert de contractuele specificaties. In deze functie ben je verantwoordelijk voor de organisatie en coördinatie van alle kwaliteitsaspecten- en procedures van de aan jou toevertrouwde projecten. Je bent het aanspreekpunt van de klant voor alle kwaliteitgerelateerde items. Je beheert het projectkwaliteitsdossier, zowel van de eigen vestigingen als van de subcontractors, maw je stelt de ITP procedures en QC procedures op, in overeenstemming met constructiecodes en klanteneisen. Dit omvat voornamelijk lastechnieken, oppervlaktebehandeling en electrical package. Je garandeert de tijdige realisatie van het as-built dossier. Bij vragen en problemen zoek je daadkrachtig naar de beste oplossingen. Je behaalde een Master diploma Industriële Wetenschappen (of gelijkwaardig). Je kunt terugkijken op minimaal 3 jaren werkervaring in relevante sectoren, bvb de staalindustrie, bouw of offshore wereld. Je hebt een excellente kennis Engels, zowel mondeling als geschreven. Je stelt u flexibel op naar werkuren en -locatie, voornamelijk in het binnenland en soms in het buitenland. Je kunt zelfstandig werken én werken in een team. Je blijft bijleren. Je behaalt objectieven omwille van een gedreven mentaliteit. Je communiceert duidelijk en direct. Je biedt zowel praktische als theoretische situaties het hoofd. Je werkt vlot samen met anderstalige collega’s. Je denkt analytisch en je hebt ruimtelijk inzicht. Je bent handig met MS Office toepassingen en navigeert vlot in een ERP omgeving. Je kunt u terugvinden in onze waarden : Daadkracht – Respect – Klantgerichtheid – Teamwork Wij bieden je naast een grote dosis fun, avontuur en uitdaging een internationale omgeving waarin initiatief en eigen inbreng echt een verschil maken. Je kan meewerken aan tot de verbeelding sprekende constructies voor de offshore windindustrie, civiele markt en olie & gas, en dit binnen een groeiende bedrijvengroep. Verder bieden we je uiteraard ook nog: een aantrekkelijk salarispakket extralegale voordelen zoals maaltijdcheques, groepsverzekering en hospitalisatieverzekering opleidingsmogelijkheden en potentiële groeikansen – we willen dat je vooruit gaat tal van leuke evenementen zoals onze jaarlijkse kerstborrel, vakantieborrel, nieuwjaarsreceptie, teambuilding, familiedag…
QA Manager (M/F) (H/F
PaHRtners, Luik, Luik (Provincie), Liège
QA Manager (M/F) (H/F/X) LIEGE Mise à jour le 15/04/2021 - Réf . : 3668643 Cadre technique de contrôle-qualité (53212) [CADRES TECHNIQUES DE PRODUCTION] Recherche et développement fr, en Non spécifié Poste(s) : 1 Situé en région liégeoise, notre client est une entreprise active dans le domaine de la santé. Présente depuis de nombreuses années, l’entreprise dispose d’une gamme de produits reconnus sur le marché international et d’un potentiel de croissance intéressant. Afin de compléter l’équipe QA, nous sommes activement à la recherche d’un (h/f) : QA Manager. Responsabilités : En tant que QA Manager, vous coordonnez et assurez le bon fonctionnement du Syste`me de Management de la Qualite´ relatif aux activite´s de production et de QC en vue de respecter les normes GMP et GDP. Les responsabilite´s suivantes vous sont confie´es : Participer à la Strate´gie Qualite´ de l’entreprise. Coordonner la gestion des de´viations, des CAPA et des change controls. Re´aliser les audits internes et externes : clients, fournisseurs et autorite´s. Superviser la libe´ration des lots apre`s analyse des dossiers de fabrication et d’analyse. Coordonner les activite´s de rappel, le cas e´che´ant. Rédiger et approuver les proce´dures des activite´s de validation et qualification des équipements. Coordonner les programmes d’ame´lioration continue. Superviser la re´daction des revues annuelles de lots. Coordonner la gestion des risques. Gérer l’équipe qualité. Rapporter re´gulie`rement l’e´volution des activite´s vers le top management. Profil : Vous êtes titulaire d’un Master en Pharmacie. Vous disposez de minimum 5 anne´es d'expe´rience QA en industrie pharma/biotech. Vous maitrisez les GMP. La connaissance des normes FDA ainsi que le numéro QP sont des atouts. Vous faites montre de leadership, dote´(e) d’un esprit fe´de´rateur, vous e^tes convaincant(e). ? Vous e^tes rigoureux/se, me´thodique, autonome. Vous e^tes dote´(e) d’une forte capacite´ organisationnelle et communicationnelle. Vous avez une bonne connaissance du franc¸ais et de l’anglais. Offre : Une fonction diversifie´e incluant des responsabilite´s et des projets inte´ressants. Des de´fis professionnels, scientifiques et humains enrichissants. Des possibilite´s de de´veloppement et d’e´volution stimulantes. Inte´grer une structure industrielle conviviale et en pleine croissance. Un salaire attractif reprenant des avantages extra-le´gaux, en ligne avec votre expe´rience. Inte´resse´(e) ? Envoyez votre CV accompagne´ d'une courte lettre de motivation via https://www.pahrtners.be/fr/offres-demploi/qa-manager/ ou a` : recruitmentpahrtners.be. Votre candidature sera traite´e en toute confidentialite´. Votre profil Langue(s) Langue Niveau Français Très bonne connaissance Anglais Bonne connaissance VOTRE CONTRAT Régime de travail : Autre régime Commentaire additionnel : Début du contrat : au plus vite Type : Non spécifié POSTULER / CONTACT PaHRtners PaHRtners Site web : https://references.lesoir.be/postuler/9868941/qa-manager-m-f-/?utm_sourceLeforem&utm_mediumaggregator
QA/QC Data Analyst
Imerys, Willebroek, Flanders
The Company The world leader in mineral-based specialty solutions for industry, with over 16,000 employees and over 200 sites worldwide, Imerys delivers high value-added, functional solutions to diversified set of industrial sectors, from processing industries to consumer goods. The Group draws on its knowledge of applications, technological expertise and its material science know-how to deliver solutions based on beneficiation of its mineral resources, synthetic minerals and formulations. These contribute essential properties to customers’ products and performance, including refractoriness, hardness, conductivity, opacity, durability, purity, lightness, filtration, absorption and repellency. Imerys is determined to develop responsibly, in particular by fostering the emergence of environmentally-friendly products and processes. If you want to grow your skills and develop your career, find out more at The Position QA/QC Data Analyst Job Summary This person is highly committed to Quality and thinks in terms of Continuous Improvement and Collaboration. He/she reports to the Quality Manager and will work closely with the QA Engineer. He/she is responsible for translating raw data of process parameters and QC results into clear reports with the usage of statistical techniques. He/she will coordinate practical action plans in order to increase stability of production quality output and reduce process variation and production costs.  POSITION RESPONSIBILITIES  Creates reports of process parameters in order to optimize production processes Creates and maintain SPC dashboards with department leaders Performs trend analysis Prepares and defines action plans, identifies and resolves problems, completes audits and define improvement actions Takes part in root cause analyses Ensures QA/QC activities are properly implemented and communicated Maintains and improves product and process quality by completing system compliance and process audits. Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions and revalidations. Validates product quality by issuing Certificates of Analysis for each shipment Supports the Imerys Safety System Together with the local I³ Champion (Imerys Industrial Improvement), implements and drives the Imerys Operational Excellence program called I³ within your area. IDEAL PROFILE A minimum of 3 years QA systems experience within Operations. Being a certified Internal / external Auditor is an asset. Strong knowledge SPC, good analytical skills Familiar with different statistical methodologies Good knowledge ISO9001:2015 Experience with following disciplines is an asset: Minitab IATF16949 Lean and 6Sigma TQM Change Management Fluent in both Dutch and English, written and oral. Good oral communication and administrative reporting skills. Ability to work effectively across multiple departments. Influential leadership skills. Very at ease with IT tools.
QA SYSTEM SPECIALIST - AUDIT EXPERT (H/F) (h/f)
MASTHERCELL, Charleroi
QA SYSTEM SPECIALIST - AUDIT EXPERT (H/F) (h/f) Ref 1347856 Based in Gosselies, the mission of Catalent Cell and Gene Therapy is to deliver optimized process industrialization capacities to cell therapy organizations, and speed up the arrival of their therapies onto the market. From technology selection to business modeling, through GMP manufacturing, process development, quality services, Catalent's teams are fully committed to helping their clients fulfill their objective of providing sustainable and affordable therapies to their patients. To lead its increasing number of development and manufacturing projects, Catalent Cell and Gene Therapy is looking for a highly motivated QA System Specialist. The Role The QA System Specialist (audit expert) will ensure the maintenance and the improvement of the Quality Management system and the compliance with applicable US/EU regulations, guidances and Catalent's policies/procedures. In life cycle phase, the QA System Specialist is focus in the maintenance of the following system : Update, in compliance with the current regulation the QA quality system documents.With the collaboration of concerned department, establish annually the Annual Quality Review (AQR).Review, challenge and approve, in compliance with GMP, Deviation, CAPA, Complains, Audits, Change Control, Risk.Update, analyze the process of deviation, capa, change control, risk analysis with KPI. Propose and realize adapted action.Ensure the internal audit program is compliant to current regulations as required. Plan, coordinate (scheduling, and reporting) and perform audits of the plant systems and procedures.Update and take adapted action to ensure the CAPA follow up.Update and realise the Self Inspection quality system documents and take adapted action to ensure the CAPA follow up.Quality Risk Management The Candidate Master degree or Bachelor degree in biology, pharmacy, clinical chemistry, etc., or relevant.Experience in a similar position in the sector of biotech/Pharma/cell therapy.Fluency in French and English is a must.Good knowledge of cGMP and audits.Experience of minimum 2-3 years in Quality Assurance, preferably in a biopharmaceutical company.Microsoft office ( Word, Excel, Power Point) , TrackWise and ComplianceWire. Soft skills Rigourous, consciencious, flexible and honest.Critical mind.Autonomous and organized (good time management skills).Efficient communicator, quality minded and customer oriented.Quality mindset Catalent's standard leadership competencies that are used to interview and for Performance & Development: Delivers Results.Leads with Integrity and Respect.Demonstrates Business Acumen.Fosters Collaboration and Teamwork.Champions Change.Engages and Inspires.Coaches and Develops Profiel - Talenkennis Français : Bon Anglais : Moyen Hoe solliciteren? MASTHERCELL Contactpersoon
QA / QC Data Analyst (SPC)
OneJob, Willebroek, Mechelen
Onze klant is een wereldmarktleider in oplossingen op basis van mineralen voor de industrie. Met de oplossingen in koolstof (carbon black) dragen wij bij tot de ontwikkeling van tal van producten in tal van sectoren.Verspreid over meer dan 200 locaties vormen we een hechte familie van meer dan 16.000 medewerkers.De organisatie maakt een sterke groei door. Om die groei te ondersteunen en nieuwe producten en materialen te ontwikkelen, is onze afdeling Kwaliteit momenteel op zoek naar een QA / QC data analist (SPC). Deze persoon is zeer toegewijd aan Kwaliteit en denkt in termen van Continuous Improvement en Collaboration.Hij/zij rapporteert aan de Quality Manager en zal nauw samenwerken met de QA Engineer.Hij/zij is verantwoordelijk voor het vertalen van ruwe data van procesparameters en QC resultaten naar duidelijke rapporten met behulp van statistische technieken.Hij/zij coördineert praktische actieplannen om de stabiliteit van de productiekwaliteit te verhogen en procesvariatie en productiekosten te verminderen. Je verantwoordelijkheden: -Rapporten maken van procesparameters om productieprocessen te optimaliseren -Creëren en onderhouden van SPC dashboards met afdelingsleiders -Trendanalyses uitvoeren -Actieplannen opstellen en definiëren, problemen identificeren en oplossen, audits voltooien en verbeteracties definiëren -Deelnemen aan root cause analyses -Ervoor zorgen dat QA/QC activiteiten correct worden uitgevoerd en gecommuniceerd -Handhaven en verbeteren van product- en proceskwaliteit door het uitvoeren van systeem compliance en proces audits. -Voorbereiden van kwaliteitsdocumentatie en -rapporten door het verzamelen, analyseren en samenvatten van informatie en trends, waaronder mislukte processen, stabiliteitsstudies, recalls, correctieve acties en revalidaties. -Valideren van de productkwaliteit door het afgeven van analysecertificaten voor elke zending. -Het veiligheidssysteem ondersteunen Minimaal 3 jaar ervaring met QA-systemen binnen Operations. Een gecertificeerde interne / externe auditor is een pluspunt. Sterke kennis SPC, goede analytische vaardigheden Vertrouwd met verschillende statistische methodologieën Goede kennis ISO9001:2015 Ervaring met volgende disciplines is een pluspunt: Lean en 6Sigma Vloeiend in zowel Nederlands als Engels, schriftelijk en mondeling. Goede mondelinge communicatie en administratieve rapportage vaardigheden. Vermogen om effectief over meerdere afdelingen heen te werken. Invloedrijke leiderschapsvaardigheden. Zeer vertrouwd met IT-tools. Een unieke kans om deel uit te maken van een wereldleider waar je de kans hebt om substantieel bij te dragen aan de creatie van nieuwe koolstofproducten en -materialen en om productieprocessen te verbeteren.Een competitief salarispakket gebaseerd op je kennis en ervaring, inclusief een aantrekkelijk pakket extralegale voordelenEen uitdagende en innovatieve werkomgevingLeuke collega's, zowel lokaal als internationaal.
QA Automation Engineer Bluetooth Configurator
Infineon Technologies AG, Львів, Lvivska, Ukraine
Job Description & How to Apply BelowPosition:  QA Automation Engineer for Bluetooth Configurator (f/m/div)*Location: ЛьвівWould you like to be part of the creation of the next generation’s state-of-the-art technologic solutions? Developing software for you is like creating a masterpiece? Join us as a Senior QA Automation Engineer and show us your mastery! Responsibilities You’ll be responsible for developing automated tests for software solutions, like Bluetooth Configurator, in order to ensure the best product solutions for our customers.In your new role you will:Take part in new test methodologies and test systems development;Perform Test feasibility  and planning tasks;Collaborate with other colleagues from different expert areas , namely software, digital hardware, operations, and marketing;Test cases  automation  via writing scripts  in Python ;Debug  issues and triage the  failures ;Support  Quality reporting ;Enable continuous improvement and innovation;Define  test strategy  and have test ownership of projects during their execution;Working in  Agile teams  and  executing assigned tasks  during sprints.Your ProfileYou have a structured working style and seek high quality standards for yourself and for others. You demonstrate strong communication skills, know how to establish lasting relationships, coordinate your work with colleagues, even across borders, and regularly share your insights with them. Moreover, you use all of your potential and capacity and challenge yourself and others to produce top performance.You are best equipped for this task if you have:Previous  e  xperience in Software/Firmware  development or  QA automation ;Programming skills in  Python ;Experience with  Test Planning, Test Case Development, and Test Methodologies ;Knowledge of  bug tracking tools  (like Jira) and  debugging methods ;Scripting language experience Bash is a plus;Fluency in  English  would be a plus.Benefits:Coaching, mentoring networking possibilitiesWide range of training offers & planning of career developmentInternational assignmentsDifferent career paths: Project Management, Technical Ladder, Management & Individual ContributorFlexible working conditionsMedical coverageOn-site gym, jogging paths, beachvolleyball, tennis & soccer courtOn-site canteenPrivate insurance offersWage payment in case of sick leaveAccess for wheelchairsTap HERE to APPLY → Go to Job Application Site ←   Search for further Jobs Here:Search here through 5 Million+ jobs:CV Search (Enter less keywords for more results. Suggestions may be selected)Location - Select a country -AlbaniaAlgeriaAndorraAngolaArgentinaArmeniaAustraliaAustriaAzerbaijanBahrainBangladeshBelarusBelgiumBeninBosnia HerzegovinaBotswanaBrazilBruneiBulgariaCambodiaCameroonCanadaCanary IslandsCaribbeanChannel IslandsChileChinaColombiaCosta RicaCroatiaCyprusCzech RepublicDenmarkDominican RepublicEcuadorEgyptEstoniaEthiopiaFijiFinlandFranceFrench PolynesiaGambiaGeorgiaGermanyGhanaGibraltarGreeceGuatemalaHondurasHong KongHungaryIcelandIndiaIndonesiaIranIraqIrelandIsraelItalyJamaicaJapanJordanKazakhstanKenyaKuwaitKyrgyzstanLatviaLebanonLibyaLiechtensteinLithuaniaLuxembourgMacedoniaMalaysiaMaldivesMaltaMauritiusMexicoMicronesiaMongoliaMontenegroMoroccoMozambiqueMyanmarNamibiaNepalNetherlandsNew ZealandNicaraguaNigeriaNorwayOmanPakistanPanamaPeruPhilippinesPolandPortugalQatarRomaniaRussiaSaudi ArabiaSenegalSerbiaSingaporeSlovakiaSloveniaSouth AfricaSouth KoreaSpainSri LankaSudanSwedenSwitzerlandSyriaTaiwanTajikistanTanzaniaThailandTrinidad TobagoTunisiaTurkeyUAE/DubaiUKUSAUgandaUkraineUzbekistanVenezuelaVietnamYemenZambiaZimbabwe - Any State -- Any City -BerehoveBilhorod-DnistrovskyiCherkassyChernigovChernivtsiChernobylDniproDonetskKerchKharkovKhersonKhmelnitskiyKhustKievKirovogradKomsomolskKryvyi RihLuganskLvivMariupolMukacheveMykolaivNikolaevOdessaPoltavaSevastopolSimferopolSumyTernopilTruskavetcUzhgorodUzhhorodVinnitsaVynohradivZaporozhyeZhytomyrEmployment Category- Select a category -AccountingAdministrative/ClericalAdvertisingAirport/AirlineArchitectureAutomotiveBankingBeauty/HairdressingBusinessChild Care/NannyingConstructionCreative Arts/MediaCustomer Service/Help DeskDentalDesign/Web/MultimediaDoctor/PhysicianESL/TEFLEducationEnergy/Power GenerationEngineeringEntertainment/GamingFinanceFreelanceGovernmentHR/RecruitmentHealthcareHospitality/CateringHotelIT/TechInsuranceLanguage/BilingualLaw/LegalMaintenance/CleaningManagementManufacturingMarketing/PRNon-ProfitNursingOil & Gas IndustryOnlineOutdoor/Nature/AnimalPharmaceuticalProductionQuality ControlReal Estate/PropertyResearch/DevelopmentRestaurant/Food ServiceRetailSalesScienceSecuritySkilled Labor/TradesSocial WorkSoftware DevelopmentSports/Fitness/WellnessSupply Chain/LogisticsTeachingTourism/TravelTransportationWarehouseFiltersEducation (minimum level)- Unspecified -High SchoolTech SchoolCollegeBachelorMastersDoctorateFiltersEducation Level Any High School Tech School College Bachelor Masters DoctorateExperience Level (years) Less than 1 Year 1 to 2 Years 3 to 4 Years 5 to 6 Years 7 to 8 Years 9 to 10 Years 10 to 15 Years More than 15 YearsPosted in last: Day Week Month Any  Only Jobs that accept applications from my present countryAdvanced Search ×
QA Automation Engineer Bluetooth Configurator
Infineon Technologies AG, Львів, Lvivska, Ukraine
Job Description & How to Apply BelowPosition:  QA Automation Engineer for Bluetooth Configurator (f/m/div)*Location: ЛьвівWould you like to be part of the creation of the next generation’s state-of-the-art technologic solutions? Developing software for you is like creating a masterpiece? Join us as a Senior QA Automation Engineer and show us your mastery! Responsibilities You’ll be responsible for developing automated tests for software solutions, like Bluetooth Configurator, in order to ensure the best product solutions for our customers. In your new role you will: • Take part in new test methodologies and test systems development; • Perform Test feasibility and planning tasks; • Collaborate with other colleagues from different expert areas, namely software, digital hardware, operations, and marketing; • Test cases automation via writing scripts in Python; • Debug issues and triage the failures; • Support Quality reporting; • Enable continuous improvement and innovation; • Define test strategy and have test ownership of projects during their execution; • Working in Agile teams and executing assigned tasks during sprints. Your Profile You have a structured working style and seek high quality standards for yourself and for others. You demonstrate strong communication skills, know how to establish lasting relationships, coordinate your work with colleagues, even across borders, and regularly share your insights with them. Moreover, you use all of your potential and capacity and challenge yourself and others to produce top performance. You are best equipped for this task if you have: • Previous experience in Software/Firmware development or QA automation; • Programming skills in Python; • Experience with Test Planning, Test Case Development, and Test Methodologies; • Knowledge of bug tracking tools (like Jira) and debugging methods; • Scripting language experience Bash is a plus; • Fluency in English would be a plus.Benefits:• Coaching, mentoring networking possibilities • Wide range of training offers & planning of career development • International assignments • Different career paths: Project Management, Technical Ladder, Management & Individual Contributor • Flexible working conditions • Medical coverage • On-site gym, jogging paths, beachvolleyball, tennis & soccer court • On-site canteen • Private insurance offers • Wage payment in case of sick leave • Access for wheelchairsTap HERE to APPLY → Go to Job Application Site ←   Search for further Jobs Here:Search here through 5 Million+ jobs:CV Search (Enter less keywords for more results. Suggestions may be selected)Location - Select a country -AlbaniaAlgeriaAndorraAngolaArgentinaArmeniaAustraliaAustriaAzerbaijanBahrainBangladeshBelarusBelgiumBeninBosnia HerzegovinaBotswanaBrazilBruneiBulgariaCambodiaCameroonCanadaCanary IslandsCaribbeanChannel IslandsChileChinaColombiaCosta RicaCroatiaCyprusCzech RepublicDenmarkDominican RepublicEcuadorEgyptEstoniaEthiopiaFijiFinlandFranceFrench PolynesiaGambiaGeorgiaGermanyGhanaGibraltarGreeceGuatemalaHondurasHong KongHungaryIcelandIndiaIndonesiaIranIraqIrelandIsraelItalyJamaicaJapanJordanKazakhstanKenyaKuwaitKyrgyzstanLatviaLebanonLibyaLiechtensteinLithuaniaLuxembourgMacedoniaMalaysiaMaldivesMaltaMauritiusMexicoMicronesiaMongoliaMontenegroMoroccoMozambiqueMyanmarNamibiaNepalNetherlandsNew ZealandNicaraguaNigeriaNorwayOmanPakistanPanamaPeruPhilippinesPolandPortugalQatarRomaniaRussiaSaudi ArabiaSenegalSerbiaSingaporeSlovakiaSloveniaSouth AfricaSouth KoreaSpainSri LankaSudanSwedenSwitzerlandSyriaTaiwanTajikistanTanzaniaThailandTrinidad TobagoTunisiaTurkeyUAE/DubaiUKUSAUgandaUkraineUzbekistanVenezuelaVietnamYemenZambiaZimbabwe - Any State -- Any City -BerehoveBilhorod-DnistrovskyiCherkassyChernigovChernivtsiChernobylDniproDonetskKerchKharkovKhersonKhmelnitskiyKhustKievKirovogradKomsomolskKryvyi RihLuganskLvivMariupolMukacheveMykolaivNikolaevOdessaPoltavaSevastopolSimferopolSumyTernopilTruskavetcUzhgorodUzhhorodVinnitsaVynohradivZaporozhyeZhytomyrEmployment Category- Select a category -AccountingAdministrative/ClericalAdvertisingAirport/AirlineArchitectureAutomotiveBankingBeauty/HairdressingBusinessChild Care/NannyingConstructionCreative Arts/MediaCustomer Service/Help DeskDentalDesign/Web/MultimediaDoctor/PhysicianESL/TEFLEducationEnergy/Power GenerationEngineeringEntertainment/GamingFinanceFreelanceGovernmentHR/RecruitmentHealthcareHospitality/CateringHotelIT/TechInsuranceLanguage/BilingualLaw/LegalMaintenance/CleaningManagementManufacturingMarketing/PRNon-ProfitNursingOil & Gas IndustryOnlineOutdoor/Nature/AnimalPharmaceuticalProductionQuality ControlReal Estate/PropertyResearch/DevelopmentRestaurant/Food ServiceRetailSalesScienceSecuritySkilled Labor/TradesSocial WorkSoftware DevelopmentSports/Fitness/WellnessSupply Chain/LogisticsTeachingTourism/TravelTransportationWarehouseFiltersEducation (minimum level)- Unspecified -High SchoolTech SchoolCollegeBachelorMastersDoctorateFiltersEducation Level Any High School Tech School College Bachelor Masters DoctorateExperience Level (years) Less than 1 Year 1 to 2 Years 3 to 4 Years 5 to 6 Years 7 to 8 Years 9 to 10 Years 10 to 15 Years More than 15 YearsPosted in last: Day Week Month Any  Only Jobs that accept applications from my present countryAdvanced Search ×
QA/QP Team Supervisor
Viatris, Hoeilaart, Halle-Vilvoorde
At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access – Providing high quality trusted medicines regardless of geography or circumstance; Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and Partnership – Leveraging our collective expertise to connect people to products and services. Every day, we rise to the challenge to make a difference and here’s how the QA Team Supervisor & RP role will make an impact: Key Responsibilities for This Role Include: The QA Team Supervisor provides substantial support to the QP/QA Director in all matters related to GMP/GDP processes and product quality for Viatris Belgium and all related entities. This person provides supervision to the appointed QA team within the QA Department. This is a key role to ensure products could be marketed in accordance with Health Authorities and Internal requirements and guidelines. EU Batch & Products Releases Preparing batch release by collecting all necessary information from suppliers as well as preparing bulk batch release and perform the first screening of the documents. Updating batch and electronic register. Interacting with external warehouse contractor to perform necessary activities. Act as RP deputy if needed. Order QC analysis with registered analytical labs and follow-up. Initiating investigation and preparing, if required, deviation reports. Organizing the collection of samples. SOP Development & Implementation according to Regional Guidelines Preparing draft SOPs. Follow-up and maintain the Viatris Global SOP System. Updating register for psychotropics and narcotics. Requesting import and export licenses. Monthly reporting to FAGG / AFMPS. Ordering sequential barcodes on request of manufacturing sites for reimbursed products. Trimonthly reporting to RIZIV / INAMI. Product Quality Complaints & Change Control Handling product quality complaints. Archive the related documentation. Coordinate change control activities, complaints and deviation process. Update technical files after approval change control. People Management & People Development Define team’s objectives and targets in order to support the business strategy together with the QA Director. Set the Yearly Objectives per team member based on yearly applicable recommendations from Europe, local General Management and Human Resources. Coach and Develop competencies & leadership expectations of the different team members by organising regular follow up moments such as: face-to-face, team meetings. Actively participate with HR to the Annual Development Plan of team members. Performance & Compensation Management: Lead the mid-year & end-year review process and participate closely with HR and QA Director to the Compensation Planning Process. Assist in organizing trainings. Follow-up on the overall training compliance status of all staff members. Update and archive training records. Qualifications and knowledge Minimum 6 to 10 years of experience within QA A few years in a leadership role is an asset Minimum of a Master of Science Degree Knowledge of national and international QA requirements and guidelines on pharmaceutical products (GDP/GMP) Software knowledge: Microsoft Office, SAP, Trackwise Fluent in English, French and Dutch, in speaking, reading, writing and presenting. Outstanding business acumen with an advanced ability to analyze business needs and transformation needs into QA actions and initiatives Able to function in a matrix environment, within a global organization, and to work closely within a local team Demonstrated ability to develop solid business partnerships with stakeholders inside and outside the company Ability to achieve results through cross-functional / cross-organizational teams Strong sense of responsibility A t Viatris, we offer competitive salar ies , benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. Viatris is an Equal Opportunity Employer. Viatris is a global healthcare company formed in 2020 through the combination of Mylan and Upjohn, a legacy division of Pfizer. By integrating the strengths of these two companies, including our global workforce of 45,000, we aim to deliver increased access to affordable, quality medicines for patients worldwide, regardless of geography or circumstance. We believe in healthcare as it should be – empowering people worldwide to live healthier at every stage of life. Because of our unwavering belief that better access leads to better health, we leverage our best-in-class manufacturing and scientific expertise and proven commercial capabilities to bring quality medicines to patients when and where they need them.