deviation

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...

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...

TheQC Department must ensure the Quality Control of all materials, intermediates, final products, according to established specifications and GMP rules. The release of the product is done according to the mentioned rules and to support the QP release. Responsibilities Execution of microbiological release analyzes for raw materials and finished...

TheQC Department must ensure the Quality Control of all materials, intermediates, final products, according to established specifications and GMP rules. The release of the product is done according to the mentioned rules and to support the QP release. Responsibilities Execution of microbiological release analyzes for raw materials and finished...

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,...

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,...

bOverview /b pIn this role you ensure GMP-compliant QA operations for Investigational Medicinal Products, focusing on documentation and quality systems. You will work with CMOs and internal stakeholders to keep batch documentation accurate, inspection-ready, and timely. You shape quality by reviewing GMP records, handling deviations, and supporting QA...

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...

Aperçu The Senior Specialist QC Compliance supports the Manager QC Compliance & Support in ensuring that QC processes are compliant with regulatory and Incyte requirements, and in contributing to their continuous improvement based on industry best practices. The activities include support related to key QC compliance processes, including deviations,...

Did you ever want to work for a company placing human at the heart of its DNA? Are you ready to make a difference? Do you feel excited about the opportunity to collaborate and share your expertise with our industry leaders? YES? SO DO WE!GXP CONSULTING Switzerland is a Swiss company with a passionate team of Life Sciences professionals. Since 2014 we deliver...

Work ScheduleFlex with On Call DutyEnvironmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety StandardsCleanroomNo hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair, etc. are not allowed. Office environment allowed. Some degree of PPE (Personal Protective Equipment) required: safety glasses, gowning,...

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...

Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of our Madrigal team is connected by our shared purpose: leading the fight...

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...

ppAre you an experienced quality compliance specialist in analytical chemistry looking to make a direct impact on life‑saving biopharmaceutical products? Join our Quality Control team in Basel to drive critical laboratory compliance, deviation investigations, and root‑cause analyses. /p h3Fully site‑based roles /h3 pThis is a fully site‑based role....

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...

Join our client and play a key role in maintaining top-tier quality standards! If you have a keen eye for detail and a passion for compliance, this could be your perfect opportunity. Proclinical is seeking a QA Associate III to join the Integrated Downstream Quality Operations team at a large-scale manufacturing facility. In this role, you will focus on...

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,...