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​ Notre client, une société biopharmaceutique privée leader dans les domaines de la santé reproductive, l'urologie, la gastro-entérologie, l'endocrinologie et l'orthopédie, recherche activement un(e) QC Validation Specialist.   ​ Responsabilités : - Réaliser des revues périodiques, des validations analytiques et des transferts de méthodes. - Rédiger la documentation liée aux activités de validation analytique (évaluation des écarts, protocoles, rapports, procédures, documentation de transfert, etc.). - Traiter les données statistiques et interpréter les résultats. - Effectuer des analyses de validation. - Collaborer avec le département d'assurance qualité réglementaire pour la rédaction des documents réglementaires. - Gérer les déviations, les CAPA et les changements selon les procédures applicables. - Mettre à jour les SOP internes. Votre profil : - Bachelor en Chimie, Pharmacie ou CFC Chimie avec minimum 3 à 5 ans d'expérience dans l'industrie pharmaceutique. - Expérience en Validation Analytique, transfert analytique ou développement de méthodes. - Compétences techniques en procédures analytiques, notamment spectrophotométrie, HPLC, GC, titrage. - Connaissance pratique avérée des pharmacopées (Ph.Eur., USP, JP) et des directives BPF et ICH. Des connaissances en affaires réglementaires sont un plus. - Langue : français et anglais (courant, parlé et écrit). - Informatique : Excellente connaissance d'Office 365 (Word, Excel), LIMS, Empower et Minitab. - Compétences générales : capacité à prendre des initiatives et à travailler de manière indépendante tout en développant et en maintenant une communication efficace avec les parties prenantes sans autorité formelle ; capacité à travailler en « mode projet » et à faire face aux changements ; réflexion stratégique. ​ Poste basé à : St-Prex (Vaud, Suisse) Contrat temporaire  Durée : jusqu'au 31 août 2026

​ MANPOWER AG ? Your Career, Our Focus! Become part of our network and take advantage of countless opportunities! ManpowerGroup is the leading global company for staffing solutions. With our three brands ? Manpower, Experis, and Talent Solutions ? we assist companies across various industries with their recruitment needs. For 75 years, we've operated in over 75 countries, and throughout Switzerland, we support our clients in successfully completing their tasks and projects. We are looking for a Data Scientist (m/f/d) (LSW) - BS   ​ Location: Basel | Workload: 100% | Start: asap (latest 1st April 2026) | Duration: 12 months | Home office: 50% |  Background Roche is seeking a skilled and proactive Temporary R&D Data Scientist to cover a maternity leave. In this position, you will maintain and further develop the internal data integration platform, support ongoing AI/ML model development, and ensure the seamless continuation of all R&D data workflows. We are looking for someone who can quickly get up to speed on complex topics, take ownership, and contribute effectively from day one. The Ideal Candidate The ideal candidate brings 3?5 years of industry experience and combines strengths in data science, data engineering, and machine learning. You are highly proficient in Python and SQL, familiar with ETL concepts, and committed to high-quality documentation and FAIR data principles. Tasks & Responsibilities - Maintain and troubleshoot existing data integration and ETL pipelines - Support AI/ML model training, validation, and optimization - Conduct data analyses, generate insights, and prepare clear research reports - Troubleshoot technical issues related to data access, software constraints, or model behavior - Ensure smooth project continuity throughout the contract period - Document all processes and system modifications in a structured and transparent manner Must Haves - Bachelor's or Master's degree in Computer Science, Data Science, Engineering, or a related quantitative field - 3?5+ years of hands-on experience in Data Science or Data Analytics - Strong proficiency in Python (Pandas, NumPy, Scikit-learn) - Experience with SQL and relational database environments - Familiarity with ETL concepts and pipeline management - Foundational understanding of machine learning models - Strong problem-solving skills and ability to work independently - Excellent communication and collaboration skills - Knowledge of FAIR data principles - Experience with image analysis techniques Next Steps - Interview process: ? 1st interview: Remote screening ? 2nd interview: Onsite - Important: The job posting will be halted on 05 March 2026 at 14:40. ​ Are you feeling unsatisfied, underchallenged, or simply ready to discover something new? What are you waiting for? Apply now, unlock your potential, and strive for greater job satisfaction. With my expertise, I am here to support you throughout the entire application process. I look forward to meeting you and hearing your story! MANPOWER AG ? Together, we shape your future!

​ 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.