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​ We are looking for a Scientist for one of our Pharma clients based in Visp.  ​ Description: Role: Timely and cGMP-compliant execution of projects within the defined area of responsibility Tasks: - Interface to the analytics representative - Correction approval in ProNas and creation of label data - Project preparation (special materials for aliquoting, checking packing lists, folders, etc.) - Assistance with and execution of trainings - Issuing reserve and stability samples - Ordering of laboratory material Responsibility: compliance with quality (SOP and GMP) and safety regulations Interfaces: QC (Quality Control), QA (Quality Assurance), AD (Analytical Development), PD (Process Development), MSAT (Manufacturing Science and Technology), Operations and Logistics - Language: English and German needed! - Experience in the needed field would be great (min. 1-2 years) - Home-office possible -QC software experience (a plus, not a must have): LIMS, Trackwise - Candidate close to Visp (Bern etc.) would be preferred / or candidates willing to relocate ​ Contact: Alba Jansa +41 61 282 22 13 alba.jansa(at)experis.ch

​ Depuis 1948, ManpowerGroup libère le potentiel des femmes et des hommes en fournissant des opportunités d'emploi, d'expérience et de formation. Fort d'un réseau mondial de 3'500 bureaux dans 80 pays du monde, ManpowerGroup vous accompagne dans votre développement professionnel. ​ Votre mission :  - Conception 3D sur logiciel CAO/FAO  - Calculs et dimensionnements (systèmes mécaniques, électriques, pneumatique, ?)  - Simulation FEM - Etude de faisabilité - Calculs et optimisation des coûts  - Gestion de projets Votre profil :  Vous êtes au bénéfice d'une formation d'ingénieur en mécanique ou microtechnique Vous assumez une expérience confirmée dans un poste similaire Vous êtes autonome, proactif-ve et faite preuve d'une bonne capacité analytique Parfaite maîtrise du français ; Allemand ou/et Anglais un atout Maîtrise d'un logiciel ERP un atout ​ Candidature :  CV, Certificats de travail, Diplômes, Permis de travail, Annexes Nous nous réjouissions de recevoir votre candidature !

​ 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 Scientific Researcher (m/w/d) (LSB) - BS - BS ​   The Ideal Candidate: The Perfect Candidate: holds a BSc or MSc in Biomedical Research and brings at least two years of relevant industry experience as a Lab Technician or Research Associate. They have hands-on experience with LIMS, biological sample reception, registration, storage and shipment, and are familiar with GCP requirements, BSL-2 laboratory environments, and ethical considerations related General Information: - Start date: 01.02.2026 - Latest Start Date: 16.02.2026 - Planned duration: 6 months - Extension: not likely (maternity leave) - Max. Bill Rate: 48.98 CHF (Depends on the experience) - Workplace: Basel - Workload: 100% - Home Office: No - Travel: No - Team: 5-10 people - Working hours: Standard Key Responsibilities: - Responsible for performing laboratory-based activities and processes - Tracking, inventory, sample processing, and transport of biological samples from clinical and non-clinical trials - Manage associated metadata, and ensuring that lab activities fulfill customer needs - Achieve operational excellence in quality, service levels, cost and compliance Must-Haves: - BSc or equivalent degree in the area of Biomedical Research (BSc/ MSc highest possible degree, no PhDs)  - 2 years relevant industry experience as a Lab Technician; Research Associates  - Demonstrated experience in the use of LIMS (Laboratory Information Management System) and related sample data handling systems  - Familiarity with GCP requirements, BSL2 (Biosafety Safety Level 2) laboratories and awareness of the ethical considerations for the use of biological samples  - Experience with biological sample reception, registration, storage and shipment  - Fluent in English - Ability to understand complex processes and recommend solutions - Team player with strong interpersonal skills and the ability to build effective working relationships - Experience assessing, tracking and fulfilling research customer needs on an operational level in an efficient and timely way with a high degree of customer orientation and ability to communicate with stakeholders on multiple levels   ​ Dissatisfied, underchallenged, or eager to discover something new? What are you waiting for? Apply now, unlock your potential, and aim for greater job satisfaction. I am here with my expertise to support you through the entire application process. I look forward to meeting you and am excited to hear your story! MANPOWER AG ? Together, we shape your future!

​ Our client Philip Morris is looking for a Sensory Evaluation Coordinator as contracted for a temporary position until 31.12.2026   ​ You are the good candidate if you recognise yourself in this job description : Purpose of the Job - Coordinate internal sensory panel(s) and store sensory data to guide and support CC product development activities and competitive intelligence assessments - Coordinate sensory training/evaluation sessions - Track, store and prepare samples & sensory data to ensure full traceability - Perform all the statistical analysis of the internal sensory evaluation activities for CC portfolio - Interpret the results from the statistical analysis and conduct the reporting for all the internal sensory evaluation panels for CC portfolio - Recommend & implement sensory methodologies improvement Skills: Must have: - Fluency in English, both written and spoken - Strong communication and collaboration skills - Demonstrating agility and effective stakeholder management - Good organizational skills and attention to detail - Proficiency in Microsoft Office tools (Word, Excel, PowerPoint, Outlook) - Proficiency in XLStat for statistical analysis Nice to have: - Background in sensory science is considered a strong asset - Familiarity with the EyeQuestion tool is a plus ​ We are looking forward your application ! 

​ MANPOWER AG ? Ihre Karriere, unser Fokus! Werden Sie Teil unseres Netzwerks und nutzen Sie unzählige Chancen! ManpowerGroup ist das weltweit führende Unternehmen für Personallösungen. Mit unseren drei Marken ? Manpower, Experis und Talent Solutions ? unterstützen wir Unternehmen in verschiedenen Branchen bei ihren Personalbedarfen. Seit 75 Jahren sind wir in über 75 Ländern tätig und unterstützen unsere Kunden in der ganzen Schweiz dabei, ihre Aufgaben und Projekte erfolgreich umzusetzen. Wir suchen einen Junior Process Data Scientist (m/w/d) ? Drug Substance Manufacturing ​ Hintergrund Für unseren Bereich Drug Substance Manufacturing in Basel suchen wir einen engagierten Junior Process Data Scientist, der sich auf die technische Umsetzung und Betreuung von Multivariater Datenanalyse (MVDA) spezialisiert. In dieser Funktion arbeitest du an der Entwicklung, Validierung und nachhaltigen Pflege statistischer Modelle, welche einen wesentlichen Beitrag zur Qualitätssicherung leisten. Gesucht wird eine Person am Anfang ihrer beruflichen Laufbahn mit fundierten Kenntnissen in MVDA sowie einem guten Verständnis biopharmazeutischer Herstellungsprozesse. Allgemeine Rahmenbedingungen - Start: schnellstmöglich - Spätester Start: 01.04.2026 - Einsatzdauer: 2 Jahre - Verlängerung: möglich - Arbeitsort: Basel - Pensum: 80?100 % - Home Office: idealerweise max. 50 % - Teamgrösse: ca. 10 Personen (Projektteam) - Arbeitszeitmodell: Standardarbeitszeit Aufgaben und Verantwortlichkeiten Modellentwicklung - Konzeption und Implementierung von MVDA-Modellen für Prozesse der Wirkstoffherstellung - Verantwortung für den gesamten technischen Aufbau der Modellarchitektur Datenaufbereitung und -strukturierung - Anwendung strukturierter Methoden zur Datenmodellierung - Sicherstellung einer sauberen Vorverarbeitung von Prozessdaten zur Vermeidung von Fehlklassifikationen Validierung und Modellpflege - Durchführung formaler Validierungsaktivitäten zur Absicherung der Modellqualität - Laufende Betreuung des Modell-Lebenszyklus und Anpassung an veränderte Prozess-Baselines Muss-Anforderungen - Bevorzugt Promotion in Chemieingenieurwesen, Chemometrie, Statistik oder Biotechnologie alternativ: Bachelor- oder Masterabschluss mit relevanter Berufserfahrung (*****) - Mindestens 2 Jahre Erfahrung im Bereich Statistik (*****) - Erste Industrie- oder Berufserfahrung (*****) - Deutsch und Englisch mindestens auf Niveau B2/C1 (*****) Wünschenswerte Zusatzqualifikationen - Erfahrung mit Open-DCP oder vergleichbaren Modellierungsplattformen (z. B. SIMCA) - Kenntnisse in R für statistische Analysen - Umgang mit Aveva PI System Explorer (OSIsoft) zur Datenabfrage ​ Unzufrieden, unterfordert oder neugierig auf etwas Neues? Worauf warten Sie noch? Bewerben Sie sich jetzt, entfalten Sie Ihr Potenzial und streben Sie nach größerer Zufriedenheit in Ihrer Karriere. Ich stehe Ihnen mit meiner Expertise zur Seite und begleite Sie durch den gesamten Bewerbungsprozess. Ich freue mich darauf, Sie kennenzulernen, und bin gespannt auf Ihre Geschichte! MANPOWER AG ? Gemeinsam gestalten wir Ihre Zukunft!

​ 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.