21 Temporary jobs found for you

Au sein du département Engineering & Maintenance, vous intégrerez l'équipe E&M Compliance & Qualification en tant que compliance. L'équipe, performante et dynamique, assure la compliance GMP au sein du département E&M.Vos Tâches :En tant que compliance, vous aurez principalement la charge de la gestion des déviations du départementVous avez la charge de la mise en place d'actions de corrections et de prévention efficacesVous serez point de contact privilég

As a MOS Compliance Expert at Merck, you will play a pivotal role in the Production department, especially in the Compliance field, by conducting critical and transversal complex investigations, ensuring data integrity, leading Corrective and Preventive Actions (CAPA), maintaining compliance with Good Manufacturing Practices (GMP), and overseeing classified environment monitoring activities. Your responsibilities will also include overseeing project qualit

Key Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scr

Caring for the world, one person at a time. inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of Johnson & Johnson work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 265 operating companies in more than 60 countries employing approximatel

Nous sommes à la recherche d’un.e Compliance Specialist Biotech pour notre client, Merck, pour une mission d’une durée de 12 mois. Votre rôle : Le/la Compliance Specialist Biotech aide à assurer la compliance au sein de l’équipe Compliance au Manufacturing Operational Support, en respectant les cGMPs, et en assurant l’exactitude de la documentation. Il contribue à maintenir les exigences qualité en participant aux Déviations, CAPAs, Change control et la re

We are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related to quality control issues, deviations, and non-conformances in our manufacturing processes.Key Resp

Für die Firma Jabil Switzerland Manufacturing GmbH in Grenchen suchen wir Betriebsmitarbeiter (m/w/d) für den Bereich Finish.In dieser Position hast du folgendes Aufgabengebiet:Bereitstellen von Werkzeugen, Kontrollmitteln und Vorrichtungen gemäss Anweisung und/oder UnterlagenAbarbeiten von Aufträgen nach Anweisung des Vorgesetzten gemäss QSKorrektes und vollständiges Ausfüllen der Produktionsunterlagen gemäss GMPKennen und Befolgen der Richtlinien bezügli

Caring for the world, one person at a time. Inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of Johnson & Johnson work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 265 operating companies in more than 60 countries, employing approximate

Für die Firma Jabil Manufacturing GmbH suchen wir in Grenchen per sofort einen CNC-Operateur 100% (m/w/d):Deine täglichen Hauptaufgaben:Einrichten, Bedienen und Überwachen von CNC Kurz- und/oder LangdrehmaschinenBereitstellen von Werkzeugen, Kontrollmitteln und Vorrichtungen gemäss Anweisungen Termin- und sachgerechte Abarbeitung nach Fertigungsaufträgen, Prüfanweisungen, Verfahrensanweisungen und ZeichnungenReinigen von Maschinen und Ausführen einfacher W

Are you looking for a challenging job as an Automation Engineer?Do you have experience working with MES Syncade? Would you like to work in the pharmaceutical sector? Our client is looking for an Automation Engineer, who would be a part of a disciplinary team. This role plays a key part in designing, testing, and troubleshooting recipes in Syncade, ensuring compliance with regulatory standards during the design, start-up, qualification, and production phase

For our client Merck in Aubonne, we are looking for a QA Specialist for QC (m/f/d) for a period of 12 months from 1st September 2024.Your role: To ensure the quality oversight and compliance of QC activities and the data integrity of QC analytical data in timely manner. QA Oversight on QC analytical data:To perform the QA review on QC analytical data, on QC documentation. Manage QC deviation, CCP and CAPA as QA.Compliance of QC activities:QA support for QC

Are you ready to bring your mechanical skills to a large healthcare manufacturing services company in Switzerland? If so, we have the perfect opportunity for you.For Jabil Manufacturing GmbH we are urgently seeking for CNC Machinists (100%) (m/f/d) for long term temporary missions (crossborder talents from neighbouring countries are welcome).Your main daily responsibilities include:Setting up, operating, and monitoring CNC short and/or long turning machine

"Die Arbeit, die du heute machst, könnte morgen Leben retten."Möchtest auch du deine mechanischen Fähigkeiten im weltweit grössten Unternehmen für Healthcare-Design und Herstellungsdienstleistungen einbringen? Dann haben wir genau die richtige Stelle für dich.Für die Firma Jabil Manufacturing GmbH suchen wir in Grenchen per sofort einen CNC-Mechaniker 100% (m/w/d):Zu deinen täglichen Hauptaufgaben gehören:Einrichten, Bedienen und Überwachen von CNC Kurz- u

Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und vereint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.DePuy Synthes Companies of Johnson & Johnson ist das größte und umfassendste Orthopädie- und Neurologieunternehmen der Welt. DePuy Synthes bietet eine beispiellose Breite und Tiefe unterschiedlicher Technologien, Produkte, Dienstl

Joining our Manufacturing Department, you will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells.As Support Technician, you will take part in this exciting adventure by supporting the Manufacturing Shared Services in our development and clinical suites.Your role: Support Operational Activities:Be the expert in the processes under our responsibility (r

An exciting new opportunity has arisen to join us as Quality Assurance Qualification & Validation Engineer for our Biotech drug substance plant in Corsier-sur-Vevey.As an integral member of the Quality Unit, you provide QA expertise for Process Validation and Analytical Validation: You elaborate the qualification/validation strategies, review and approval of protocols and reports, participates to risk analysis, identifies gap and purposes remediation plan

Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und vereint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.DePuy Synthes Companies of Johnson & Johnson ist das größte und umfassendste Orthopädie- und Neurologieunternehmen der Welt. DePuy Synthes bietet eine beispiellose Breite und Tiefe unterschiedlicher Technologien, Produkte, Dienstl

Tasks:Lead and execute medium-sized customer projects and internal projects, ensuring complianceProject planning and technical detailing of gas-insulated switchgear, including preparation of all necessary documents for orders, fabrication, assembly, and customers.Discuss and align technical solutions with customers and internal stakeholders.Manage all technical communication channels, both internally and externally.Oversee project execution and material pr

For our client, a pharmaceutical company based in canton Lucerne, we are looking for a Labelling Coordinator. General Information: Start Date: ASAPDuration: 1 yearExtension: possibleWorkload: 100%Workplace: canton LucerneHome office: up to 2 days/week, but mainly onsite The primary activities include, but are not limited to: Creation of label text translations using a translation database and approval of the translations regarding study-specific, company-i

For our client, an international biotech company based in Baar, we are looking for a Regulatory Affairs Senior Manager to join the Biosimilars Business Unit. The person will be responsible for leading regulatory affairs activities for assigned projects and programs and for leading affiliate RA to identify and complete national regulatory requirements for assigned projects and programs, to support commercialisation.General Information: Start date: ASAP / 02

For our client, an international company in Zürich, we are looking for a Quality Manager.General Information: Start date: ASAP/30.09.2024End date: 31.03.2026Extension: to be discussedWorkplace: ZürichHome office: possible, hybrid roleWorkload: 100%Responsibilities: Drive and support analytical method life cycle management (LCM) strategy for in-process, release and stability testing of commercial productsLeads multisite assay transfers via providing assay t