Trova lavoro per Industria farmaceutica in Svizzera, Solothurn:4
29/09/2026 Nuovo!
| Svizzera, Soletta, Solothurn - Manpower |
| 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 (e.g., 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 +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. |
23/09/2026
| Svizzera, Soletta, Soloithurn - Manpower |
| 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. |
18/09/2026
| Svizzera, Soletta, Solothurn - Manpower |
| 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. |
09/09/2026
| Svizzera, Soletta, Solothurn - Manpower |
| 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. |