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.
As a Quality Assurance Associate, you will contribute to maintaining and strengthening the Quality Management System at the Solothurn site. In this role, you‘ll support core quality activities, help coordinate routine governance processes, and assist in maintaining inspection readiness. You will collaborate with various site or global functions to ensure smooth execution of essential quality tasks. This position allows you to play an important part in sustaining a strong culture of compliance without carrying full ownership of operational responsibilities.
The holder of this position will be responsible for the following activities:
1. Audit and Inspection Support
Coordinate and monitor audit and inspection commitments to ensure timely closure and proper documentation in line with Biogen QMS requirements.
Organize and facilitate meetings with SMEs to review action status, gather updates, and maintain alignment on deliverables.
2. Site Meeting Governance
Schedule and manage logistics for site governance meetings ( , Investigation Review Board), including agenda preparation, pre‑read collection, and documentation of decisions.
Support governance forums related to deviations, change controls, CAPAs, and other QMS review boards to ensure consistent application of Biogen standards.
Contribute to improving and optimizing governance meetings in line with site objectives
3. Self‑Inspection Program Execution
Assist in planning, implementing, and tracking the Self‑Inspection Program, including scheduling activities with SMEs and ensuring timely documentation and follow‑up of observations.
Maintain tools and trackers supporting inspection readiness and compliance monitoring.
4. QMS Administration & Operational Support
Support QMS processes including deviations, CAPAs, change controls, training assignments, and quality risk management in accordance with Biogen procedures.
Collaborate with cross‑functional stakeholders (QA, QC, Manufacturing, Engineering, etc.) to ensure compliance and timely completion of required actions.
Support on KPIs reporting and monitoring
5. Documentation & Data Management
Ensure accurate and compliant documentation of QMS activities in systems such as TrackWise, Veeva, and myCIMS.
Maintain logs, trackers, meeting minutes, dashboards, and metrics related to QMS processes and governance activities.
Identify opportunities to streamline QMS processes, improve documentation quality, and enhance visibility of compliance commitments.
This position requires co-operation with people at every level of the organization and from multiple functions, including engineering, automation, validation, Manufacturing personnel, SME‘s on equipment and knowledge of biotechnology API production.
Good communication skills in English, verbally and written.
Self-driven and take ownership and responsibility for own assignments. Value teamwork at all levels, performs work with an open-mind and ability to value input from colleagues and peers. Able to drive discussion to solve problems with cross functional teams.
Be confident in making technical decisions. In addition, must be able to prioritize tasks, be flexible and able to keep many activities running at a time.
If you are interested in this opportunity, we look forward to receiving your CV or if you have any questions, contact Elaine Kanwar at .
Check out all open positions at Experis at
Due to Swiss work permit restrictions, we can only consider applications from EU citizens or holders of valid working permit in Switzerland.
Vedi dettagli
Industria farmaceutica
Risorse umane
Mappa
47.20813557.5384045
Altri annunci di lavoro pubblicati da questa azienda
Planificateur/trice-électricien/ne CFC ? Lausanne, Suisse
Dans le c?ur de la Suisse romande, nous concevons et réalisons des installations électriques fiables, performantes et durables. Notre culture repose sur la qualité d'exécution, la précision des dossiers et un travail d'équipe solide entre les bureaux d'études et le terrain. Nous croyons aussi à une approche inclusive : chaque parcours compte, et nous encourageons la diversité des profils à contribuer à des projets concrets. Vos responsabilités
Réaliser et mettre à jour les plans et schémas électriques (courants forts et/ou faibles) selon les besoins du projet
Concevoir les dossiers de planification : implantation, cheminements, schémas unifilaires, nomenclatures et schémas de câblage
Préparer la documentation technique pour les phases d'étude, d'exécution et de mise en service
Garantir la cohérence des plans avec les exigences techniques, les normes applicables et les contraintes chantier
Collaborer avec les ingénieurs, chefs de projet et équipes terrain pour assurer la faisabilité et la conformité
Participer aux revues techniques et contribuer à la résolution des écarts entre conception et réalisation
Assurer le suivi de l'avancement documentaire et la traçabilité des versions et des modifications
Contribuer à l'optimisation des solutions (choix des composants, organisation des câbles, simplification des dossiers)
Compétences et qualifications requises
CFC d'installateur-électricien
Maîtrise approfondie du logiciel Revit
Maîtrise des logiciels informatiques usuels, Autocad, Polylog, Office, Relux, etc. ;
Expérience confirmée en planification électrique et production de plans conformes aux exigences projet
Maîtrise des outils de conception et de documentation (CAO/DAO) pour la création de schémas et plans
Connaissance des normes et exigences techniques applicables en Suisse (lecture et application)
Capacité à lire, interpréter et exploiter des schémas électriques et des plans d'exécution
Rigueur, sens du détail et aptitude à travailler avec des dossiers structurés et des versions maîtrisées
Bon niveau de français, à l'oral comme à l'écrit, pour communiquer efficacement avec les équipes
Autonomie, sens des responsabilités et respect des délais avec une qualité constante
Connaissance des principes de gestion documentaire (naming, versions, contrôles) pour assurer la traçabilité
Esprit d'analyse pour identifier les incohérences et proposer des ajustements pragmatiques
Ce que vous trouverez chez nous
Des projets concrets, avec une forte exigence de qualité et de clarté dans la documentation
Un environnement collaboratif, où l'amélioration continue est encouragée
Une culture inclusive et respectueuse, ouverte à des profils aux parcours variés
Des échanges techniques réguliers pour progresser et consolider vos compétences
Postulez dès maintenant
Si vous souhaitez mettre votre expertise de planification au service de projets électriques exigeants et contribuer à une équipe qui valorise la diversité et la qualité, nous serions ravis de recevoir votre candidature. Envoyez votre dossier et indiquez votre disponibilité pour rejoindre notre équipe à Lausanne.
Verkaufsleiter Industrie (m/w/d) 100% | Deutschschweiz
Für ein erfolgreiches Industrieunternehmen mit starker Marktposition suchen wir im Rahmen einer exklusiven Suche eine unternehmerisch denkende Führungspersönlichkeit für die Leitung des Vertriebs.
In dieser Schlüsselrolle übernehmen Sie die Verantwortung für die strategische und operative Weiterentwicklung des Verkaufs, führen ein bestehendes Team und tragen massgeblich zum weiteren Wachstum des Unternehmens bei. Ihre Verantwortung
Führung, Coaching und Weiterentwicklung des Vertriebsteams
Ausbau bestehender Kundenbeziehungen auf strategischer Ebene
Akquisition und Entwicklung neuer Geschäftsmöglichkeiten
Verantwortung für Umsatz, Budget und Vertriebsergebnisse
Entwicklung und Umsetzung von Markt- und Verkaufsstrategien
Zusammenarbeit mit Geschäftsleitung und relevanten Stakeholdern
Identifikation von Markttrends und Wachstumspotenzialen
Ihr Profil
Technische oder betriebswirtschaftliche Ausbildung mit entsprechender Weiterbildung
Mehrjährige Führungserfahrung im Vertrieb eines Industrieunternehmens
Nachweisbare Erfolge im Business Development und Key Account Management
Unternehmerische Denkweise und hohe Eigenverantwortung
Sicheres Auftreten auf Management-Ebene
Sehr gute Deutschkenntnisse, weitere Sprachen von Vorteil
Das erwartet Sie
Schlüsselposition mit direktem Einfluss auf die Unternehmensentwicklung
Hoher Gestaltungsspielraum und kurze Entscheidungswege
Etabliertes, innovationsstarkes Industrieunternehmen
Attraktive Anstellungsbedingungen
Moderne und flexible Arbeitsmodelle
Diese Position richtet sich an ambitionierte Verkaufsleiter, Senior Key Account Manager oder Vertriebsleiter mit Führungsverantwortung, welche den nächsten Karriereschritt in einem anspruchsvollen industriellen Umfeld suchen.
Vertrauliche Kontaktaufnahme
Aziz Cakan
Senior Branch Manager | Executive Search
Manpower Schweiz
ž +41 79 477 63 05
✉️ aziz.cakan@manpower.ch
La posizione:
La risorsa si occuperà delle attività di fusione e trasformazione dei metalli attraverso impianti e forni industriali, contribuendo al corretto svolgimento del processo produttivo nel rispetto degli standard qualitativi e di sicurezza. Principali responsabilità:
Conduzione e monitoraggio di forni industriali per la fusione di metalli;
Preparazione delle materie prime e gestione delle fasi di lavorazione;
Pulizia, manutenzione ordinaria e cura delle attrezzature e dell'area di lavoro;
Supporto alle attività del reparto e collaborazione con il team di produzione;
Requisiti richiesti:
Esperienza pregressa in contesti produttivi;
Disponibilità al lavoro su turni;
Disponibilità a lavorare in ambienti caratterizzati da elevate temperature;
Capacità di lavorare sia in autonomia sia all'interno di un team;
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.
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.
For one of our Pharma clients based in Visp, we are looking for an
EI&C PI Engineer
JOB DESCRIPTION
Key Responsibilities
Administer and maintain PI Data Archive, interfaces, connectors, and supporting infrastructure.
Configure and support PI Asset Framework (AF), templates, hierarchies, attributes, and Event Frames (EF).
Develop and maintain PI Analytics, KPIs, calculations, and data evaluation solutions.
Design, implement, and troubleshoot interfaces between PI and systems such as DeltaV, PLCs, MES, LIMS, and enterprise applications.
Develop integrations and applications using PI SDK, AF SDK, PI Web API, REST APIs, and SQL-based solutions.
Support data sharing and reporting platforms including Power BI and other analytics tools.
Ensure system reliability through monitoring, troubleshooting, lifecycle management, upgrades, and patching.
Create and maintain GxP-compliant documentation, support validation activities, and ensure data integrity compliance.
Collaborate with Automation, Manufacturing, Engineering, Data Analytics, and IT teams on initiatives.
Required Qualifications
Degree in Automation Engineering, Electrical Engineering, Computer Science, Information Technology, or similar.
Strong IT background including servers, databases, networking, virtualization, and system integrations.
Hands-on experience with:
PI Data Archive
PI Asset Framework (AF)
Event Frames (EF)
PI Interfaces & Connectors
PI Analytics
PI SDK / AF SDK / PI Web API
Experience in GMP-regulated environments and GxP documentation.
Strong analytical, troubleshooting, and problem-solving skills.
Fluent English and/or German.
Preferred Qualifications
Experience in pharmaceutical or biotech manufacturing.
Knowledge of DeltaV, MES, SCADA, and industrial automation systems.
Experience with Power BI, SQL databases, and data analytics platforms.
Understanding of OT cybersecurity and data governance principles.
Key Competencies
Cross-Functional Collaboration
Additional Information:
100% Site based VISP
1-year contract with possibility of extension
Digital Manufacturing & Industry 4.0
Troubleshooting & Root Cause Analysis
IT/OT Infrastructure
GMP Documentation & Validation
System Integration & APIs
Data Analytics & Reporting
PI AF & Event Frames
Process Data Historian Management
PI System Administration
If you are interested and believe you are a good fit, do not hesitate to contact me directly: alba.jansa@experis.ch
JOB DESCRIPTION
EI&C Software Application Engineer
Key Responsibilities
Develop, configure, and maintain automation and manufacturing software applications.
Design, implement, and integrate solutions connected to DCS, MES, historians, databases, and related manufacturing systems.
Develop software solutions using technologies such as VBA, PowerShell, C#, SQL, and Git-based version control systems.
Create software design specifications, functional specifications, and other engineering documentation in accordance with GMP and company standards.
Support system interfaces, data exchange, and integration between OT and IT platforms.
Execute software testing, commissioning, qualification, and deployment activities.
Participate in troubleshooting, root cause investigations, and resolution of software and system issues.
Maintain and enhance existing applications to improve reliability, performance, and user experience.
Collaborate with Automation, Manufacturing, Validation, Quality, and IT teams throughout the project lifecycle.
Ensure compliance with cybersecurity, data integrity, and change management requirements.
Required Qualifications
Degree in Automation Engineering, Electrical Engineering, Computer Science, Information Technology, or a related discipline.
Strong IT background with knowledge of software development, databases, networking, and system integrations.
Experience with automation and manufacturing systems such as DCS, MES, or data historian platforms.
Knowledge of programming and scripting languages including VBA, PowerShell, C#, and SQL.
Understanding of software lifecycle management and application support.
Experience working in GMP-regulated environments and creating GxP-compliant documentation.
Strong analytical, troubleshooting, and problem-solving skills.
Fluent English and/or German.
Preferred Qualifications
Experience in pharmaceutical, biotechnology, or life sciences manufacturing.
Knowledge of DeltaV, Syncade, PI System, or similar industrial software platforms.
Familiarity with software validation, CSV/CSA methodologies, and data integrity requirements.
Understanding of OT infrastructure and cybersecurity principles.
Key Competencies
Software Development & Application Support
DCS & MES Integration
Database Management & SQL
VBA, PowerShell & C# Development
GxP Documentation & Validation
System Testing & Commissioning
Troubleshooting & Root Cause Analysis
IT/OT System Integration
Change Management & Version Control
Cross-Functional Collaboration
Additional Information:
100% Site based VISP
1-year contract with possibility of extension Contact: Alba Jansa
alba.jansa@experis.ch
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.
Location: Solothurn
Start date: ASAP
Duration: 12 months Key Responsibilities The Warehouse Operator/Materials Handler performs and documents daily Materials Management operations and internal material flow activities in a cGMP environment. The role involves all floor operations in the Warehouse & Weigh & Dispense department. The associate maintains a safe, efficient, and productive environment across warehouse and dispensary operations, with strong attention to detail and documentation while maintaining required trai ning levels. The Material Handler is expected to support cross-functional operations, with movement between the Warehouse and Weigh & Dispense areas determined by business needs and Supervisor direction.
Other information:
-Team structure: The team consists of 17 members.
-Languages: English is mandatory.
-Certifications: Forklift license is required.
-Tools: Experience with Oracle and Syncade is required.
-Schedule: Standard hours; no shift work is expected.
If you are interested in this opportunity, we look forward to receiving your CV or if you have any questions, contact Elaine Kanwar at +41 61 282 22 23
Check out all open positions at Experis at www.experis.ch
Due to Swiss work permit restrictions, we can only consider applications from EU citizens or holders of valid working permit in Switzerland.
The role:
The Associate III within the Integrated Downstream Quality Operations team is being part of the Quality Department at the new Large-Scale Manufacturing facility located at the Solothurn/Switzerland site. He/She focuses on Quality Operations and Quality Engineering activities for downstream manufacturing and equipment. The Solothurn site is intended to operate with a fully integrated electronic batch record for all commercial, clinical and PPQ campaigns.
General Information:
Start Date: 01.11.2026
End Date: 31.03.2027 (extension planned)
Location: Solothurn
Department: Quality Assurance, Integrated Downstream Quality Operations
Responsibilities:
- Executes QA activities related to downstream operations, GMP manufacturing, and downstream equipment to ensure the safety, efficacy and purity of the products manufactured by Biogen
- Reviews and approves GMP Engineering and Manufacturing documents during both project and operational phases of the site, specifically related to procedures, work instructions, CAPAs, deviations, change control, equipment (work orders, P&IDs, qualification protocols, calibration deviations..,) etc.
- Partners with Manufacturing, Manufacturing Sciences, Process Engineering, Automation SMEs during deviation management and investigations.
- Take part to the monitoring and release activities for Column Packing / Unpacking and Chromatography Review.
- Ensures adherence to internal procedures during downstream manufacturing operations or for equipment controls and release before and during GMP CAPEX and OPEX project (i.e., shutdowns, construction projects) or New product introduction
- Take part of the Quality On-Call duty rotation for Quality
- Participates in batch record review and close out in the view of batch release.
- Experience with Quality Assurance, Equipment Qualification, Downstream Process is preferred.
- Demonstrated ability to work autonomously with cross-functional team members.
- Strong presentation and organizational skills
- Demonstrated writing skills
- Demonstrated problem solving skills
- English B1 as a minimum.
If you are interested, please apply with a copy of your CV.
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
General Information:
Start Date: 21.09.2026
End Date: 28.02.2027
Location: Luterbach, Solothurn
Shift work: 5 Shift rotation (including nights)
- Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents.
- Ensuring compliance to cGMP as well as maintaining equipment and facilities.
- The Manufacturing Associate is detail-oriented with strong documentation skills. Maintain training level to the required level and support other functions on site.
- Assist with daily manufacturing operations in manufacturing facility. Typically requires 3-5 years of experience.
- The employee will be responsible for executing manufacturing related work within Solothurn as per procedures and policies.
- The employee will be accountable for maintaining and complying with the environmental, health and safety regulations.
- The employee will be responsible for maintaining his/hers training curriculum and not perform tasks that the employee is not trained to perform.
- Be able to work independently and with minimal direction. Has moderate responsibility.
- The employee will be responsible for maintaining equipment and perform manufacturing activities. Erroneous work can impact product integrity result in batch failures and consequently harm patients.
- The employee must be able to demonstrate the ability to independently document and record information related to their job functions.
- The employee must at all times make sure that if the employee is in doubt that the employee's supervisor or manager is consulted. Good verbal and written skills are required to ensure proper description of any issues.
- Employee must collaborate well with supporting functions and seek to define best outcomes for patients and the facility.
- A basic knowledge of biopharmaceutical technology and processes. The employee must be able to follow and comply with procedures and protocols.
- The employee should occasionally be able to make routine decisions based on gained experience. The employee must have a solid understanding of the requirements within correct and timely documentation within a cGMP environment.
- The employee must be trained and skilled in all operational and regulatory procedures of manufacturing department.
- Employee understands importance of safety and can teach saftey principles to less experienced colleagues.
If you are interested, please reply with a copy of your CV.
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.
Location: Solothurn
Start date: ASAP
Duration: 12 months Key Responsibilities The Warehouse Operator/Materials Handler performs and documents daily Materials Management operations and internal material flow activities in a cGMP environment. The role involves all floor operations in the Warehouse & Weigh & Dispense department. The associate maintains a safe, efficient, and productive environment across warehouse and dispensary operations, with strong attention to detail and documentation while maintaining required trai ning levels. The Material Handler is expected to support cross-functional operations, with movement between the Warehouse and Weigh & Dispense areas determined by business needs and Supervisor direction.
Other information:
-Team structure: The team consists of 17 members.
-Languages: English is mandatory.
-Certifications: Forklift license is required.
-Tools: Experience with Oracle and Syncade is required.
-Schedule: Standard hours; no shift work is expected.
If you are interested in this opportunity, we look forward to receiving your CV or if you have any questions, contact Elaine Kanwar at +41 61 282 22 23
Check out all open positions at Experis at www.experis.ch
Due to Swiss work permit restrictions, we can only consider applications from EU citizens or holders of valid working permit in Switzerland.
