Aktuelle Jobs im Zusammenhang mit QA Operation Specialist - CorsiersurVevey - Randstad
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QA Operation Specialist
vor 2 Monaten
Corsier-sur-Vevey, Schweiz Randstad VollzeitDescription du postePour notre client basé à Corsier-sur-Vevey, au seinde l'équipe QA Operations, nous sommes à la recherche de plusieursQA Operations Specialist pour une durée de 12 à jusqu'à 24 mois.En tant que membre de l'équipe, vous assurez laconformité et la documentation des activités de lié à lafabrication sur le site. Vous travaillerez...
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Quality Assurance Specialist
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Corsier-sur-Vevey, Schweiz Randstad VollzeitJob DescriptionWe are seeking a highly skilled Quality Assurance Specialist to join our team at Randstad. As a key member of our Quality Unit, you will provide QA expertise for Process Validation and Analytical Validation.You will develop qualification/validation strategies, review and approve protocols and reports, participate in risk analysis, identify...
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Quality Assurance Specialist
vor 1 Monat
Corsier-sur-Vevey, Schweiz Randstad VollzeitJob DescriptionWe are seeking a highly skilled Quality Assurance Qualification & Validation Expert to join our team at Randstad. As an integral member of the Quality Unit, you will provide QA expertise for Process Validation and Analytical Validation:You will develop and implement qualification/validation strategies, review and approve protocols and reports,...
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QC Project
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Corsier-sur-Vevey, Schweiz Randstad VollzeitJobdescriptionAs part of the QC Project & Equipment team , yourwill be able:To coordinate QCactivities related to outsourcing Technology transfer and/orroutine analytical activities .To ensure thatall QC testing related to Tech Transfert are performed according tothe established plan, good manufacturing practices, registrationproduct files and site quality...
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Director, Engineering
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Quality Assurance Specialist
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Villars-sur-Glâne, Freiburg, Schweiz Corden Pharma - A Full-Service CDMO Vollzeit{"h2": "Join Our Team as a QA Specialist CordenPharma International (CPI) is a leading Contract Development and Manufacturing Organization (CDMO) that develops and produces active pharmaceutical ingredients, medicines, and associated packaging services on behalf of its customers as a full-service provider. We are seeking a highly skilled QA Specialist to...
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Quality Assurance Specialist
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Gmpl-0, Scientist
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Corporate Engagement
vor 3 Wochen
Vevey, Schweiz Nestlé SA VollzeitPress Tab to Move to Skip to Content Link Corporate Engagement & Events Specialist Position Snapshot Location: Vevey, Switzerland Company: Société des Produits Nestlé S.A.Act. Rate: Full-Time Type of contract: Temporary contract, 9 months What we offer at Nestlé Flexible work arrangements. Please talk to us during the recruitment process...
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Quality Assurance Specialist
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Corporate Engagement
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Vevey, Schweiz Nestlé VollzeitPosition SnapshotLocation: Vevey, SwitzerlandCompany: Société des Produits Nestlé S.A.Act. Rate: Full-TimeType of contract: Temporary contract, 9 monthsStart date: 1.12.2024What we offer at NestléFlexible work arrangements. Please talk to us during the recruitment process about what flexibility could look like for you!Genuine opportunities for career and...
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Quality Assurance Specialist
vor 2 Wochen
Villars-sur-Glâne, Freiburg, Schweiz Corden Pharma - A Full-Service CDMO VollzeitQuality Assurance Specialist - Fixed-Term 4 MonthsCordenPharma, a leading Contract Development and Manufacturing Organization (CDMO), is seeking a Quality Assurance Specialist to join their team on a fixed-term basis for 4 months. The successful candidate will be responsible for ensuring compliance with data protection regulations, reviewing batch records,...
QA Operation Specialist
vor 2 Monaten
Description du poste Pour notre client basé à Corsier-sur-Vevey, au sein de l'équipe QA Operations, nous sommes à la recherche de plusieurs QA Operations Specialist pour une durée de 12 à jusqu'à 24 mois. En tant que membre de l'équipe, vous assurez la conformité et la documentation des activités de lié à la fabrication sur le site. Vous travaillerez en étroite collaboration avec la Production, les fonctions Supports (Data, Engineering, Maintenance, Supply…) ou le partie Process libération. Votre rôle : Être le référent QA pour les déviations et donner les requis pour les les enquêtes/investigation associées Évaluer et clôturer les déviations mineures/majeures et identifier les récurrences Assister et approuver à la définition des actions correctives et préventives (CAPA) Examiner et approuver les documents GMPs lié à votre role. Examiner, approuver et suivre la documentation cGMP et les propositions de changement (CCP) Participer aux inspections des autorités de santé et aux audits corporatifs et internes Respecter les indicateurs qualité afin de libéré les lot à temps pour nos patients et nos clients. Functie-eisen Votre profil : Formation scientifique (master de préférences) en biologie, chimie, ingénierie pharmaceutique ou équivalent 3 ans d'expérience dans l'industrie pharmaceutique ou biopharmaceutique sur un site de fabrication GMP Excellente connaissance des Bonnes Pratiques de Fabrication (cGMP) et des environnements contrôlés Compétence processus qualité et utilisation avec les outils d'investigation (exemple: Trackwise et SAP) Doté.e d'un bon niveau de français et d'anglais, vous êtes reconnu pour votre assertivité, votre capacité à collaborer en équipe et votre proactivité dans la mise en ?uvre d'améliorations. Orienté résultats
