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​ Established in 1948 in Milwaukee, Wisconsin (USA), Manpower is a global leader in the human resources industry. Operating in 82 countries with a network of over 3,900 offices, the company supports the workforce needs of more than 400,000 clients worldwide. As specialists in the recruitment and selection of permanent and temporary professionals across all major economic sectors, we have been operating in Switzerland for over 60 years, employing more than 260 professionals across 37 locations nationwide. On behalf of our client, we are looking for a QA Specialist. ​ Tasks and responsibilities: - Take ownership of all Quality Assurance aspects within company projects, with a strong focus on qualification and validation (e.g., moulding and assembly processes, new/modified manufacturing processes and environments, software systems). - Lead and support quality-related activities in projects by motivating collaborators, working across cross-functional and cross-site teams, and documenting decisions with clear justifications. - Apply relevant compliance standards (FDA, GMP, ISO 13485, ISO 15378, ICH) to ensure alignment with internal requirements and customer expectations. - Ensure the preparation, accuracy, and integrity of quality documentation related to qualifications and validations, maintaining traceability and compliance across all records. - Plan and prioritize qualification/validation project phases (e.g., DQ/IQ/OQ/PQ, risk assessments, protocols/reviews, Validation Master Plans) to meet critical deadlines, applying project management skills. - Investigate and resolve deviations and anomalies using a structured problem-solving approach, proactively proposing effective solutions. - Evaluate process data objectively with statistical tools to support risk-based and compliance-driven decisions. - Act as a key representative in managing qualification/validation strategies and activities with customers, notified bodies, regulatory authorities, and internal stakeholders. - Support the Quality Assurance team in other QA activities and processes (e.g., CAPA, Change Control, Complaints) as well as in Continuous Improvement initiatives. QUALIFICATIONS - Technical background (ideally with a degree in Mechanical Engineering or a related field) - Background in validation and qualification within pharmaceutical and/or medical devices environments - Good knowledge of pharmaceutical regulations such as GMP, ISO 13485, ISO 15378, FDA, ICH - Experience in industrial manufacturing processes (preferably components assembly and plastic moulding), quality control, and project management - Ability to use statistical and data analysis tools - Strong quality mindset with a risk-based decision-making approach - Proven leadership, teamwork and communication skills - Good command of English, both spoken and written ​ PLEASE REGISTER YOURSELF AND UPLOAD YOUR CV AT OUR OFFICIAL WEBSITE: WWW.MANPOWER.CH, IN ORDER TO PROCESS YOUR APPLICATION.

​ Notre partenaire, une société biopharmaceutique privée, leader dans les domaines de la santé reproductive, l'urologie, la gastro-entérologie, l'endocrinologie et l'orthopédie, est à la recherche de candidats qualifiés pour le poste de QC Lab Analyst.  ​ Vos missions : En tant que QC Lab Analyst, vous jouerez un rôle essentiel dans le maintien de la qualité des produits de l'entreprise. Vous serez en charge des responsabilités suivantes : - Effectuer des analyses physico-chimiques sur les produits intermédiaires et semi-finis ; - Assurer la revue analytique des données brutes des tests et des dossiers de lot QC ; - Rédiger et mettre à jour la documentation QC ; - Participer à la déclaration et aux investigations de laboratoire ; - Contribuer à l'amélioration continue et Lean en proposant et en mettant en ?uvre des solutions ; - Participer à l'implémentation de CAPA et de change control ; - Garantir un environnement de laboratoire sûr et conforme aux normes 6S.   Profil recherché : - Titulaire d'un CFC en Chimie ou équivalent, avec 3 à 5 ans d'expérience en Industrie Pharmaceutique ; - Connaissances des méthodes chromatographiques (HPLC et GC) ; - Expertise en méthodes d'analyse physico-chimique, en particulier la dissolution ; - Excellentes capacités de communication, de rédaction, et un sens aigu de la rigueur ; - Aptitude à travailler en équipe et à rechercher le compromis. ​ Poste basé à St-Prex (Vaud, Suisse)  Date d'entrée : janvier ou février 2026 Durée : 6 mois (contrat temporaire)