JobCourier annunci per settore: Industria farmaceutica

​ Description: Der Standort in Visp, Schweiz wächst kontinuierlich und für unsere Biologics Organisation sind wir derzeit auf der Suche nach einem Bioprocess Engineer für die pharmazeutische Produktion. In dieser Rolle sind Sie zuständig für die Abwicklung von Produktionskampagnen im Produktionsbetrieb zur Herstellung von Biokonjugaten PCP (Potent Compound Production). ​ Ihre Aufgaben: · Als Bioprocess Engineer/Biotechnologe/Chemiker (w/m/d) sind Sie für die korrekte Durchführung von Produktionskampagnen nach cGMP-Richtlinien zuständig · Review der Risikoanalyse und Umsetzung der daraus resultierenden Maßnahmen · Sicherstellung der Chargenausführung, Auswertung der Testergebnisse, Behebung von Problemen, Fehlerbehebungen von Fertigungsanlagen, sowie die Abgabe von Lösungsvorschlägen · Vollständige Dokumentation der Prozesse und des Prozess Know-hows, sowie vollständige GMP-Dokumentation · Erstellung der Kampagnenberichte und die Mitarbeit an Annual Product Review's · Kontinuierliche Verbesserungsmöglichkeiten der Prozesse, Anlagen und Abläufen, in Zusammenarbeit mit verschiedenen Projektteams wie R&D, MSAT zur Steigerung der Prozesseffizienz und zur ökonomisch Nutzung der Anlagen · Verantwortlich für die Ausbildung der Mitarbeiter bei den zugewiesenen Produkten (Kampagnenschulung), sowie die Mitverantwortung für die Schulung der Mitarbeiter, bei projektübergreifenden Themen (Quartalsschulungen, Spezialthemen) und im täglichen Betrieb Ihr Anforderungsprofil: · Bachelor-/Masterabschluss (Uni / FH) oder Promotion ? bevorzugt in Biotechnologie, Biochemie, Chemie o.ä. · Erste Berufserfahrung in der pharmazeutischen, biotechnologischen oder in der industriellen Produktion wünschenswert · Fließende Deutsch- und Englischkenntnisse · Gutes GMP-Verständnis · Team- und Führungsqualitäten, sowie sehr gute Kommunikationsfähigkeiten · Cross-funktionale, strukturierte und fokussierte Arbeitesweise · Talent für Organisation, Proaktivität und Aufgeschlossenheit für neue Ideen und Anregungen Fliessend Deutsch & Englisch min. C1 ​ Kontakt: Alba Jansa alba.jansa(at)experis.ch +41 61 282 22 13  

​ General Information: Tasks & Responsibilities: Clear description of responsibilities: owning the E2E schedules for programs (Operational readiness) including workload, updating the resources workload for PCP operation (manufacturing building in Visp) , Lead the meeting with internal stakeholders (QA, QC, Ops, MSAT, Plant. Eng, support team,...) for E2E schedule update and tracking Project background / context: support/own the planification of the different projects (operational readiness NOT CAPEX) and support others tasks not only related to scheduling Key internal and external stakeholders: No external stakeholders only internal (Lonza and especially PCP team)   ​ Must-Haves: Years of relevant industry experience: 5 years minimum Specific tools/systems (e.g., Primavera P6): full autonomy P6 and good practice on excel Mindset or working style (e.g., data-driven) open mindset, curious on data, develop schedule on primavera and excel Nice-to-Haves: Soft skills (e.g., strategic agility, feedback culture): confortable in challenging people, pro-active, lead meeting for building schedule and execution, knowledge of pharmaceutical environment is a plus (operation/manufacturing) Project methodology / leadership experience: Leadership to support the team to build a realistic schedule, need to have a good methodology knowledge, able to accept to go in the detailes schedule at tasks level as needed ​ If you are interested and believe you are a great fit, do not hesitate to contact me directly:  alba.jansa(at)experis.ch +41 61 282 22 13

​ Nous recherchons pour notre client spécialisé dans l'industrie chimique, un technologue en production chimique (H/F) ayant un diplôme en chimie.  ​ Tâches :  - Assurer la conduite des réacteurs de synthèse et/ou équipements de distillation lors d'opérations batch - Travail en zone ATEX dans le strict respect des règles HSE - Chargement manuel des matières dans les appareils à partir de fûts, conteneur mobiles et sacs - Différentes opérations a réalisé : dosage de réactifs, décantation, distillation, concentration, transfert, filtration, lavage, etc ... - Surveillance et ajustement des appareils - Contrôle des produits en cours de fabrication (prise d'échantillon, interprétation des résultats) - Utilisation de SAP  Vous êtes : - Diplomé en chimie ( CFC, TFIC, CAIC...) - Autonome sur les différents process de la chimie - Mobile sur le canton de Genève - Disponible sur des horaires de journée ou d'équipe ​ Si vous êtes intéressé(e) et correspondez au profil recherché, vous pouvez vous inscrire directement en transmettant votre dossier complet (CV - diplômes - certificat de travail).

​ Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers.   ​ On behalf of our global Pharmaceutical client based in Basel, we are looking for a technically strong data professional with solid experience in data engineering, data warehousing, and database management, including hands-on expertise with NoSQL databases such as MongoDB. Strong Python scripting skills and practical experience with ETL orchestration tools are essential. The ideal candidate has a good understanding of Text Analytics, Text and Data Mining (TDM), and Large Language Models (LLMs), and is familiar with applying FAIR principles in data workflows. Experience with scientific or other text-based data, high-performance computing environments, and API development (e.g., GraphQL) is highly desirable. A biomedical background is a plus. General Information: ? Start Date: asap ? Latest Possible Start Date: 01.06.2026 ? Planned Duration of Employment: 12 months ? Extension (for temporary contracts): Likely if budget gets approved ? Workplace: Basel ? Workload: 100% ? Home Office: partially possible Tasks & Responsibilities: ? Designing and implementing the ETL pipeline and MongoDB scheme. ? Managing the document database, data curation, and FAIRification (cleaning, parsing, disambiguation, deduplication, data harmonization etc.), including ongoing database maintenance. ? Integrating new data sources, including the development of robust parsers and text cleaning workflows. ? Enhancing the user experience (e.g., building a data warehouse and APIs). ? User support for utilizing RoMine datasets (documentation, training, use case support). Must Haves: ? Data engineering, data warehousing, and database experience  ? Experience with NoSQL/MongoDB database.  ? Good understanding in the area of Text Analytics/Mining, TDM, and LLMs. ? Experience or knowledge of ETL orchestration tools, such as Airflow.  ? Strong proficiency in Python scripting. ? Knowledgeable on the FAIR principles and associated methodology. ? Familiarity with scientific literature/published content/literature or/and other text-based data ? Excellent communication and interpersonal skills in English (fluent), German is nice to have. ? Interdisciplinary teamwork, ability to explain technical concepts to non technical stakeholders ? Exposure to high-performance computing environments. ? Experience with API development (e.g., GraphQL API) is a plus. ? Biomedical background/education is a plus ​ If you are interested in this opportunity, please apply with a copy of your CV or feel free to reach me at +41 61 282 2223

​ Founded in 1948 in Milwaukee, Wisconsin, USA, Manpower is a leading international human resources company. Located in 75 countries worldwide, with over 3'000 branches, Manpower responds to the needs of its 400'000 customers. Specialists in the recruitment and selection of permanent and temporary personnel in various economic sectors, we have been existing in Switzerland for over 60 years with more than 300 employees in more than 40 branches. For our estimated client, we are looking for an experienced Executive Assistant available part-time. ​ Main Responsibilities: - Manage the Event Sponsorship trackers, ensuring information is always up to date and assist in the production of sales/logistics information for sponsors - Collection of POs for invoicing and successful administrative processing of sponsorship assignment emails. - Send out preliminary reminders for the marketing content/materials related to the purchased sponsorship products and services and keep track of the follow-ups in the respective trackers. - Involved in level 1 evaluation phase of the marketing content/materials related to the purchased sponsorship products and services. - Answer promptly to general email queries concerning sponsorship activities and acknowledge receipt and process marketing materials  - Prepare Industry Site Visit ? Document creation support, send invitations, collect requests and setup meetings on site. - Compile accurate minutes after each industry meeting for the assigned congress or Industry Site Visit. - Provide administrative support namely: travel bookings, expense claim consolidation and relevant PO generation. - Report back to Head of Events Sponsorship Department. Experience & Skills: - Good interpersonal communication skills and ability to work effectively in an international team - Proficiency in MS Office programs and MS Outlook - Proven work experience within the Events and Healthcare Industries a plus - Strong project management and time management skills are essential - Desire to work in the sponsorship and events arena - Willingness to take ownership and responsibility for all allocated tasks - Customer orientated and commitment to customer satisfaction Ability to: - multi-task and consistently to deliver high-quality work to timescale - build and maintain strong working relationships with clients, partner suppliers and colleagues - think around issues by providing solutions, not problems - Might be required to travel in Europe/other regions in order to attend congresses and industry meetings up to 2 weeks per annum with overnight stays (With one stay of at least 4 consecutive nights). - C2 written and spoken English ​ PLEASE REGISTER YOURSELF AND UPLOAD YOUR CV AT OUR OFFICIAL WEBSITE: WWW.MANPOWER.CH, IN ORDER TO PROCESS YOUR APPLICATION.

​ Mandaté par notre client spécialisé dans le domaine de la stérilisation sur le Canton de Vaud, nous sommes activement à la recherche d'un(-e) Assistant(-e) technique en stérilisation.   ​ Votre mission : Au sein d'une structure experte dans le domaine de la stérilisation, vous jouez un rôle central dans la gestion opérationnelle et la qualité des prestations délivrées. À ce titre, vous serez amené(-e) à : - Coordonner et sécuriser les flux de transport ainsi que la circulation des analyses entre les différents sites clients - Veiller à la mise à disposition, dans les délais définis, de dispositifs stériles conformes et opérationnels pour l'ensemble des services et partenaires - Accompagner et sensibiliser les équipes aux bonnes pratiques et aux exigences liées à la stérilisation - Apporter votre expertise en matière de retraitement des dispositifs médicaux et agir comme interlocuteur(-trice) de référence auprès des services internes et des structures externes - Gérer les flux logistiques liés aux lits, au linge, aux tenues professionnelles ainsi qu'à l'organisation des vestiaires Votre profil : - Expérience dans le domaine de la stérilisation et du lavage - Sens des responsabilités et respect strict des procédures - Rigueur, organisation et esprit d'équipe - Bonne capacité de communication et aisance dans la transmission d'informations - Capacité à travailler dans un environnement exigeant et structuré ​ Cliquer sur le bouton en ligne pour postuler en toute simplicité. Nous nous réjouissons de recevoir votre candidature et prendrons contact avec vous dans les plus brefs délais.

​ Welcome to a leading company in the pharmaceutical manufacturing industry, recognized for its commitment to quality, compliance, and operational excellence. We offer you the opportunity to work in a highly regulated and professional environment where your expertise is valued and your attention to detail makes a real impact on patient safety and product quality. Our organization places strong emphasis on GMP standards, teamwork, and continuous improvement. You will collaborate closely with cross-functional teams to ensure timely and compliant batch release while contributing to a culture built on precision, accountability, and open communication. Join our dedicated team in Visp and help ensure the highest standards in pharmaceutical manufacturing. ​ Description Making sure the batch was made properly, according to procedure and regulatory requirements. Reviewers should have great attention to detail, be able to work independently, and have a thorough knowledge of the manufacturing process they are reviewing. Tasks - Review paperbased executed batch records within the specified timeframe. - Track, report and monitor batch record review and other relevant critical metrics to ensure on-time batch release. - Raise meetings with Ops related observations in a timely manner. Skills - Professional experience in GMP production environment, quality procedures and SOP execution and/or Bachelor's/Master's Degree or equivalent experience. - Preferred area of study: Pharmaceutical Technology, Biotechnology, Chemistry, Pharmacy or equivalent scientific degree. - Experience in batch record review is highly preferred. - GMP experience (min. 2 years) - Great communication skills Additional Information - On-Site in Visp (no home office) ? Paper based - Business fluent German is a MUST - English preferred ​ Due to Swiss Employment regulations, for this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport. Interested? I look forward to receiving your application!

​ Nous recherchons pour notre client spécialisé dans l'industrie chimique, un cariste avec SUVA (H/F). ​ Vous allez : - travailler sur le quai d'arrivage ou d'expedition  - procéder à la palettisation et l'emballage des palettes  - procéder au chargement/déchargement des camions  - Remplissage des citernes (contrôle des vannes, prise d'échantillon) - trier des déchets - gérer les stocks (FIFO) - respecter des règles de sécurités  - être polyvalent sur un poste en équipe - Expérience professionnelle idéalement  dans le secteur de l'industrie       pharmaceutique, chimique ou agroalimentaire - Connaissance en logistique  - Connaissance SAP un atout - Français courant - Habitué au travail en équipe (2*8 / 3*8) - Vous devez OBLIGATOIREMENT détenir le permis cariste SUVA ​ Si vous êtes intéressé(e) et correspondez au profil recherché, vous pouvez vous inscrire directement en transmettant votre dossier complet (CV - diplômes - certificat de travail).

​ Background: The assignment will be for the Computational Sciences Center of Excellence (CS-CoE) organization of a leading Pharmaceutical company in Basel. They are conducting the award-winning ?Target Evaluator? project, in close collaboration with colleagues from Translational Medicine Neuroscience, focusing on the implementation of the requirements from the project. The project is integrating select open-source multi-agent systems towards a comprehensive, unbiased ranking framework for new target proposals. The perfect candidate: We are looking for someone with a Bachelor's or Master's degree in Computer Science, Engineering, Information Systems, Bioinformatics, or equivalent professional experience. The ideal candidate has 5+ years of Python programming, 3+ years of REST API design experience, and excellent English communication skills. The perfect candidate is proactive, analytical, highly adaptable, and thrive in cross-functional teams, quickly learning new technologies to tackle complex technical challenges. General Information: ? Start date: asap ? latest Start Date: 1.5.2026 ? Planned duration: 31.12.2026 ? Extension (in case of limitation): possible ? Workplace: Basel ? Workload: 100% ? Home Office: 2 days max. remote Tasks & Responsibilities: ? Provide agile software development services for the ?Target Evaluator? project according to the project plan. ? Provide technical consulting services to support the project team. ? Develop and implement robust backend functionalities that meet defined business needs ? Design and implement APIs for the "Target Evaluator" ? Integrate with other applications, working out technical details independently with other teams ? Research and apply new data processing and analysis techniques ? Improve quality through performance evaluation, implementation of testing strategies, and tooling Must Haves: ? Bachelor/Master degree in a relevant field such as Computer Science, Computer Engineering, Mathematical Engineering, Information Systems, or Bioinformatics is preferred. Candidates with extensive professional experience in the field can also be considered. ? Python programming (5+ years) ? Experience in REST API design (3+ years) ? Some experience in ML engineering in e.g. life sciences ? Experience in CI/CD using GitLab ? Experience in GitOps ? Experience in Kubernetes for hosting of services ? Experience in implementing user interfaces ? Working in HPC environments ? Knowledge of LLMs and LLM-based multi agent frameworks ? Excellent communication skills in fluent English, both written and verbal ? Strong collaborative approach and a desire to work effectively within a cross-functional team environment. ? Proactive and analytical mindset for identifying, troubleshooting, and resolving complex technical issues. ? High adaptability and a commitment to quickly learning new technologies and methodologies to meet evolving project needs and priorities.   ​ If you are interested, please rea y ​ Due to Swiss Employment regulations, for this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport. Interested? I look forward to receiving your application!    

​ Wir suchen einen Polymechaniker für einen unserer Pharma-Kunden mit Sitz in Visp, Schweiz. ​ Description: Am Standort Visp wird zur Verstärkung der Werkstätten ein Polymechaniker (m/w/d) gesucht. Ihre Aufgaben: ?Fachgerechte und wirtschaftliche Instandhaltung von Maschinen und Anlagenteilen nach technischen Zeichnungen und Skizzen ?Behebung von Störungen an den Anlagen ?Koordination der Arbeitsabläufe in Abstimmung mit dem Team und den Auftraggebern Ihr Anforderungsprofil: ?Abgeschlossene Ausbildung zum Polymechaniker EFZ oder einem artverwandten Beruf ?Automatikkenntnisse von Vorteil ?Bereitschaft zu kontinuierlicher Weiterbildung ?Freude an abteilungsübergreifender Arbeit sowie selbstständiges und flexibles Arbeiten im Team ?Zuverlässigkeit, Belastbarkeit sowie unternehmerisches Handeln und offene, direkte Kommunikation ?Deutschkenntnisse in Wort und Schrift sowie Englischkenntnisse. ​ Kontakt: Alba Jansa +41 61 282 22 13 alba.jansa@experis.ch

​ Nous recherchons pour notre client spécialisé dans l'industrie chimique, un technologue en production chimique (H/F) ayant un diplôme en chimie.  ​ Tâches :  - Assurer la conduite des réacteurs de synthèse et/ou équipements de distillation lors d'opérations batch - Travail en zone ATEX dans le strict respect des règles HSE - Chargement manuel des matières dans les appareils à partir de fûts, conteneur mobiles et sacs - Différentes opérations a réalisé : dosage de réactifs, décantation, distillation, concentration, transfert, filtration, lavage, etc ... - Surveillance et ajustement des appareils - Contrôle des produits en cours de fabrication (prise d'échantillon, interprétation des résultats) - Utilisation de SAP  Vous êtes : - Diplomé en chimie ( CFC, TFIC, CAIC...) - Autonome sur les différents process de la chimie - Mobile sur le canton de Genève - Disponible sur des horaires de journée ou d'équipe ​ Si vous êtes intéressé(e) et correspondez au profil recherché, vous pouvez vous inscrire directement en transmettant votre dossier complet (CV - diplômes - certificat de travail).

​ Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers. ​ Implementation Workstream Lead Background: The Overall Implementation Lead is the central orchestrator responsible for the successful end-to-end rollout of the new customer engagement platform. As the leader of the Implementation Squads Workstream, you will provide strategic direction, managing its integrated plan, budget, and resources, and representing the workstream in key leadership forums. You will own the integrated Implementation strategy and master rollout plan, coordinating the sequence, timing, and dependencies for all affiliates and functions. A key part of this is to drive stakeholder alignment, acting as the primary point of contact for affiliate leadership and global stakeholders to ensure Implementation readiness, manage expectations, and communicate progress. You will also champion a "globally consistent, locally relevant" approach, establishing the process for managing local requirements and variations without compromising the core global solution. As the primary driver of execution, you will provide cross-squad oversight for all Business Implementation Squads, ensuring they have clear plans and are executing effectively. This requires you to proactively manage all program-level risks, issues, and dependencies, driving resolution and owning the escalation path to leadership. To ensure a seamless transition from "build" to "live" operations, you will define, manage, and track the comprehensive 'go-live' readiness criteria and checklist. This is achieved by working in lock-step with the ECL, Business Process, and RDT (IT) workstreams to ensure all training, communications, and support plans are fully aligned and executed in time with the Implementation schedule. The perfect candidate brings several years of experience in large-scale program deployment or hands-on project management, with a proven track record of managing technology implementation projects. Also we are looking for someone with an outstanding stakeholder engagement and communication capabilities, with a proven ability to foster trust and ensure clear, consistent communication with both local teams and central program leadership. General Information: ? Start date: asap ? latest Start Date: 15.04.2026 ? Planned duration: 2.5 years ? Extension (in case of limitation): yes ? Workplace: Basel ? Workload: 100% ? Home Office: 2 days onsite minimum ? Travel: 20% global Tasks & Responsibilities: ? Hold accountability for the successful execution of the deployment plan in your assigned affiliate, including the on-time delivery of all local milestones from pre-launch to hypercare exit. ? Build and maintain a strong, trusted partnership with affiliate leadership and their project team, acting as their single point of contact and strategic guide. ? Lead the performance of the local implementation squad, ensuring the team is motivated, aligned, and effectively resolving all on-the-ground challenges. ? Manage the accurate tracking and reporting of all local business and technical readiness, and proactively mitigate all local risks and issues. ? Consider the local business continuity plan, ensuring that the cutover and go-live phases cause minimal disruption to critical business operations. ? Ensure the local change and training plan is delivered effectively, partnering with ECL and local champions to drive user adoption. ? Represent the affiliate's unique needs and challenges back to the central program, ensuring they are clearly communicated and appropriately addressed. Must Haves: ? University Degree in Business, IT, or a related field. ? 5-7 years of experience in large-scale program deployment or hands-on project management, with a proven track record of managing technology implementation projects. ? Experience in the pharmaceutical/biotechnology industry is strongly preferred, with a deep understanding of affiliate/local market operations, business processes, and culture. ? 3 years of matrix leadership of distributed teams; you must be able to lead and motivate a local squad without direct authority. ? A "roll-up-your-sleeves" mindset with a proven ability to identify, analyze, and resolve on-the-ground challenges and roadblocks in a fast-paced environment. ? Excellent stakeholder engagement and communication skills, with the ability to build trust and maintain clear, consistent communication with both local teams and central program leadership. ? Hands-on experience in supporting the delivery of local training and change activities to drive user adoption. ? VACC mindset and an openness to new ways of working. ? Able to travel to affiliate/market sites as needed for key milestones (e.g., go-live). ? English fluent is a MUST, other languages are a big PLUS (e.g. French, Spanish, Italian, German)   ​ For this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport. If you are interested, kindly send us your CV today through the link in the advert.

​ Fondata nel 1948 a Milwaukee, Wisconsin, USA, Manpower è una società internazionale leader nel settore delle risorse umane. Presente a livello mondiale in 82 paesi con oltre 3'900 filiali risponde ai bisogni dei suoi 400'000 clienti. Specialisti nel reclutamento e nella selezione di personale fisso e temporaneo in diversi settori dell'economia, siamo presenti in Svizzera da oltre 60 anni con più di 260 collaboratori in più di 37 sedi.  Il nostro cliente ci ha incaricato di selezionare il seguente profilo professionale: Regulatory Affairs Specialist ​ Requisiti  - Esperienza minima di 3 anni nel ruolo di Regulatory Affairs Specialist in ambito farmaceutico - Esperienza comprovata di interazione diretta con Autorità Regolatorie internazionali quali: FDA, Swissmedic, Health Canada, SFDA - Pregressa esperienza nella preparazione del modulo 1, inclusi stampati e mock-ups - Buona conoscenza dei principali strumenti informatici e software di Regulatory Affairs - Must have: e-CTD Manager Extedo  Competenze tecniche  - Gestione di procedure di Lifecycle Management di una MA application (esempio: renewal, promotional review, compliance) - Gestione di procedure regolatorie quali: MAA, Variations, Scientific Advice, Orphan Designation, Paediatric Requirements - Gradita esperienza nella gestione delle sezioni pre-cliniche e cliniche dei dossier registrativi (Moduli 4 e 5) Formazione e competenze  - Laurea in discipline scientifiche (CTF, Farmacia, Biotecnologie o affini) - Ottima conoscenza della lingua inglese scritta e parlata - Precisione, autonomia organizzativa e capacità di interfacciarsi con stakeholder internazionali ​ SE RITIENE DI POSSEDERE TUTTI I REQUISITI RICHIESTI, NON ESITI AD ISCRIVERSI E A CANDIDARSI SUL NOSTRO SITO UFFICIALE: WWW.MANPOWER.CH, ALLEGANDO IL SUO CURRICULUM VITAE.

​ Synergie Production Operator Expérience dans l'industrie pharmaceutique en inspection visuelle ou dans l'industrie horlogère requise. Information complémentaire : travail en horaires d'équipe 2x8. ​ Le technicien de production a pour objectif principal de réaliser les activités liées au processus d'inspection visuelle manuelle d'une substance pharmaceutique active. Il doit être capable de : ? Respecter les normes cGMP, BDP et EHS ? Réaliser les activités process de routine et hors routine (complétion planning) d'inspection visuelle manuelle ? Remonter les problématiques techniques et/ou organisationnelles ? Assurer le partage de connaissance avec les collègues ? Proposer des idées d'amélioration continues ? Assurer le maintien de l'état des zones de production Responsilities - Responsable de respecter les normes cGMP, BDP et EHS - Responsable du suivi de sa formation - Responsable de la bonne exécution de son travail - Responsable de remonter les problèmes rencontrés - Être à 100% autonome sur les activités de sa zone de travail - Être impliqué dans l'amélioration continue - Respect et application des leaderships behaviors - Respect des processus organisationnels Qualifications - BAC + 2 (options biotechnologie, chimie, biologie, biochimie) ou équivalent - Bonnes connaissances dans le procédé suivant : inspection visuelle manuelle ou contrôle sur loupe binoculaire - Idéalement CFC de technologue en production chimique et pharmaceutique ou diplôme équivalent. - Idéalement, une première expérience réussie dans l'industrie pharmaceutique, agroalimentaire, chimique ou horlogère. - Connaissance des règles de Bonne Pratiques de Fabrication (cGMP) - Connaissance de l'environnement de travail en zone à atmosphère contrôlée - Connaissances des logiciels du pack office (Outlook, Excel, Word, PWP) - Bonne communication verbale et écrite en français (niveau minimum B2) Soft Skills - Bonne communication verbale et écrite - Méthode et rigueur dans le travail - Disponibilité et flexibilité - Sens de l'organisation - Caractère dynamique et volontaire - Esprit d'équipe - Ownership   ​ Please Contact: elaine.kanwar@experis.ch +41 61 282 22 23

​ Services The objective of this resource within the Quality Ops organization is to provide support as a Quality Assurance Senior Expert in the frame of implementation of a new Fill and Finishing. He/she could also be involve in routine GMP operations for Fill and Finishing area. He/she must ensure the quality of information reported within the various systems and documentation with respect to current guidelines, compliance and regulatory requirements.   ​ This resource will be specifically responsible for the following tasks: - Approve on the floor aseptic interventions performed by manufacturing during Aseptic Process Simulation. - Review Master Batch Records. - Attend all meetings relevant to perform the above-mentioned tasks. - Respect the escalation process. - Other tasks related to conventional quality oversight might be occasionally requested to support the team (e.g. continuous improvement initiatives, GMP tour in classified areas, etc.). The above-mentioned tasks are site-based and on-site presence is expected. Home office might be allowed occasionally for specific tasks upon request. Profil recherché - Formation académique technique et scientifique (bac +5) - 2?3 d'expériences opérationnelles cGMP dans un département Qualité Ops sur un site de production Pharmaceutique de produits stériles injectables. - Connaissances holistiques des procédés de production (de la culture cellulaire à la répartition aseptique) : étapes unitaires, équipements, gowning, contrôles d'environnement, tests laboratoires physicochimiques et biologiques, etc. - Connaissance des référentiels Qualité (cGMP) et des Systèmes Qualité (Déviations, CAPA, Change Control, Training, Documentation, etc.) - Capacité rédactionnelle pour des documents en français et/ou anglais - Langues : français et anglais - Travail sur PC et connaissances pack Microsoft - Travail en équipe - Agilité et autonomie Mode de travail - Minimum 4 jours sur site - Reporting au QA manager, mais travail en interaction quotidienne avec Manufacturing, Engineering, Sterility Assurance, Quality Ops, Training, etc. - Horaire de 2*8 à prévoir pendant les tests de simulation aseptique ​ If you are interested, please apply with a copy of your CV at the earliest. This job will halt to accept applications end of February. Interviews will be online and 2 rounds.