deviation

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...

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...

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...

Liebherr Group is seeking a highly skilled engineer to drive engine component testing both in the workshop and on test benches, across development phases. You will analyze results, prepare standardized reports, and work closely with component technicians and cross-functional teams.You will collect validation plans, translate requirements into test cycles,...

Merck & Co., Inc. in Lucerne (Schachen/Werthenstein) seeks a Specialist Upstream Operations to support GMP manufacturing of early-stage biologics and to integrate with an existing team.You will set up and execute upstream processes, manage deviations and CAPAs, and drive continuous improvement while collaborating with QA, IT systems, and manufacturing...

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...

QA Validation Manager – Visp, Switzerland Contract: Until the end of 2026 Extension: Option to renew The Role We are looking for an experienced QA Validation Manager to join a pharmaceutical/biotechnology environment in Visp. The successful candidate will provide QA oversight across validation activities, ensuring critical GMP processes remain compliant...

MSD in Switzerland (Schachen site) is seeking an experienced compliance professional to lead GMP deviation resolution, change controls, and risk management within manufacturing. The role emphasizes cross-functional collaboration with Manufacturing, Quality, Engineering and MSAT, ensuring inspection readiness and robust CAPA definitions.Fluent German and...

Lonza Stein is seeking an experienced QA professional to provide direct oversight of the Quality Control Microbiology team, ensuring GMP-compliant operations and ongoing improvement of cGMP processes on site.You will drive the gLIMS implementation, review SOPs, manage deviations and changes, and support regulatory inspections with a pragmatic, data-driven...

Associate Scientist - QC – Laboratory Investigations & Deviations Are you ready to play a key role in maintaining the highest quality standards in pharmaceutical manufacturing? We are looking for a Temporary Associate Scientist - QC to lead lab investigations and manage minor deviation reports at our Visp site. This is a fully site‑based role. Working...

ppWir sind ein junges, dynamisches Consulting-Unternehmen mit Fokus auf die Life-Science-Industrie und arbeiten täglich an hochwertigen, praxisnahen Lösungen für unsere Kundinnen und Kunden. /ppWir bieten fundiertes Engineering-Quality-Know-how für die Implementierung oder Verbesserung des gesamten technischen Qualitätskonzepts in der...

ph31-Year Temporary Assignment | Pharmaceutical Industry | Boudry /h3 /brpFor an international pharmaceutical company in the Neuchâtel area, we are looking for a motivated QA Specialist who would like to further develop their expertise in Quality Operations and External Manufacturing. /p /brpThis is an excellent opportunity for a QA professional with first...

Lonza in Visp, Switzerland, seeks a QC professional to lead and coordinate quality control activities within the Ibex Solutions complex. You will work with manufacturing, QA and external customers, supporting campaigns and deviations under GMP.Proven expertise in GMP, QC operations and project coordination is expected, with strong communication in English...

Lonza in Stein, Switzerland, is seeking a Process Expert to lead technical troubleshooting on an aseptic filling and lyophilization line. You will drive process improvements, train operators, manage deviations, and shape a new line from PQ through Swissmedic approval with significant autonomy.You will collaborate with MSAT, QA and Engineering, ensuring...

Lonza's Basel site is offering a fix-term contract as QA Expert Analytics DP within Drug Product Services (DPS). Based in Basel and Stein, Switzerland, the role focuses on QA support for GMP-compliant analytical testing laboratories, including physicochemical and bioassay testing.You will review and approve deviations, OOS investigations, CAPAs, Change...