deviation

Kinetics Process Consulting GmbH is seeking experienced Commissioning, Qualification, and Validation professionals for pharmaceutical and biopharmaceutical projects in Switzerland. You will develop strategies, prepare and review lifecycle documentation, and provide technical leadership across the project lifecycle.Responsibilities include supporting DQ, IQ,...

Cilag AG in Schaffhausen, part of Johnson & Johnson Innovative Medicine, seeks an Operations Specialist - Non-Conformances Coordinator to manage deviations, investigate root causes, and implement corrective actions to ensure product quality.You will collaborate with production, QA, MSAT and other functions to drive continuous improvement, develop trainings,...

pLonza Basel is seeking an experienced quality compliance specialist in analytical chemistry to drive compliance and operational excellence within our QC laboratories supporting biopharmaceutical manufacturing. /ppYou will lead end-to-end deviation investigations, root-cause analysis (RCA) and CAPA plans, write and manage Quality Change Requests, and act as...

Studer Cables AG in Däniken is transforming its ERP landscape for cable manufacturing. You will provide technical and disciplinary leadership to a production team, plan shifts and vacations, and monitor quality to remedy deviations quickly.Training staff on machinery and processes completes your day, with a focus on continuous improvement. You combine...

Lonza in Visp, Switzerland, is seeking a Senior Qualifying Specialist to contribute to commissioning, qualification, and validation of new process equipment and facilities. You will drive continuous improvement, support audits, and ensure compliant operations in a fast-paced GMP environment.Responsibilities include developing qualification documents,...

Werthenstein BioPharma GmbH in Schachen, Lucerne, is seeking a Specialist Compliance Excellence to support GMP compliance and quality systems for biologics manufacturing. The role focuses on deviation investigations, change controls, risk management, and continuous improvement, with collaboration across Manufacturing, Quality, Engineering, and MSAT.The ideal...

The QA Validation Manager is responsible for ensuring all critical GMP processes are validated and maintained in compliance with product requirements, process parameters, and global regulatory guidelines. The role works closely with MSAT, Manufacturing, and clients to provide scientifically sound, documented evidence that processes will perform as required,...

bOverview /b pIn this role you will serve as the primary Quality and Compliance representative for the Disposable Kits RD team, ensuring Design Control and QMS requirements are applied across development and lifecycle activities. You will advise on engineering changes, product modifications, and sustaining work, while supporting VV planning and execution....

bOverview /b pIn this role, you ensure QA oversight for Lonza’s Visp facilities, focusing on shared utility systems, logistics, and cGMP-compliant operations. You will collaborate with cross-functional teams to uphold quality standards across utilities, cold-chain, warehousing, and product movement. You lead deviation review processes and assess CAPAs,...

pBavarian Nordic in Bern, Switzerland seeks an experienced Head of QA Operations, Product Batch Flow to lead eight QA specialists and ensure compliant, timely batch readiness. You will partner with Manufacturing, QC, Supply Chain, MSAT, and Compliance to drive quality excellence and operational efficiency. /ppThe role emphasizes risk-based decision making,...

gloor&lang AG seeks an experienced MSAT professional for a 6‑month contract in Biologics Drug Product manufacturing, focused on sterile Fill & Finish. The role requires hands‑on expertise, strong deviation handling, and collaboration with CMOs to maintain GMP standards.You will apply CPV, trending, and risk tools while supporting process robustness and...

pLonza in Visp, Switzerland seeks a QA professional to review electronic batch records (eBRs) and ensure GMP-compliant, complete batch data for QA release. You will verify process steps, identify deviations, and support CAPAs and investigations while collaborating with cross-functional teams. /ppThe role requires a Bachelor’s degree in a technical field,...

bOverview /b pAs Director, Project Controls you will lead the preparation and monitoring of complex schedules for large-scale data centre construction projects. You will ensure schedule accuracy and deliver progress reports to stakeholders, and identify deviations with corrective actions. You’ll coordinate internal and external schedules, evaluate...

bOverview /b pIn this role you coordinate with cross-functional teams to qualify and validate analytical equipment, support maintenance and calibration, and handle initial troubleshooting for laboratory instruments. You will author and support SOPs, change controls, and deviation investigations, ensuring accurate documentation and adherence to quality...

bOverview /b pIn this role you drive validation testing of engine components across development phases, translating test needs into structured cycles and overseeing result reporting. You collaborate with technicians and cross-functional teams to ensure robust validation, continuous improvement of test procedures, and transparent handling of deviations. Based...

bOverview /b pAs a Senior QA Specialist, you will ensure GMP-compliant API production and advise multiple departments on quality requirements. You will support contract manufacturing and act as a quality focal point during client GMP audits. You’ll drive deviations investigations, change controls, and continuous improvement of the Quality Management...

pulli12 months contract with extension optionbr/ /li /ululliInternational biotech company /lili12 months contract with extension optionbr/ /li /ulh3About Our Client /h3pFor our client, an international biotech company in Lucerne area, we are looking for a Solution Supply Specialist (a). This role offers a perfect balance between technical office work...

ppRoche Schweiz schlägt die Brücke zwischen Pharmazie und Diagnostik. Wichtige Forschungs- und Entwicklungsfunktionen sind hier angesiedelt. Für unsere langjährige Kundin, die F. Hoffmann - La Roche AG in bBasel /b, suchen wir eine/n /p h3bLabor Spezialist/in biotechnologische Wirkstoffproduktion /b /h3 pbHintergrund: /bbr/Am Standort Basel Drug...

Kanadevia Inova in Zürich seeks an experienced Project Scheduler to lead and manage scheduling across the full EPC lifecycle, from tendering to closeout, ensuring on-time delivery and contractual alignment.You will develop integrated schedules for engineering, procurement, construction and commissioning, monitor CPM performance, and provide progress...

Novartis Pharma Stein AG is seeking a temporary 12-month role located in Stein to support deviations, complaints, CAPAs, and production issue decisions. You will assist in creating manufacturing instructions, maintain BOMs, and ensure GMP‑compliant documentation while contributing to SOP development and validation activities.Fluency in English and German...