deviation

Senior Deviation Specialist 80%-100% (m/w/d) Senior Deviation Specialist The actual location of this job is in Visp, Switzerland. Join Lonza's Quality organization in Visp and play a critical role in ensuring the quality, compliance, and reliability of life-saving therapies. As a Senior Deviation Specialist, you will lead complex investigations, drive...

Lonza in Visp, Switzerland, is seeking a Senior Deviation Specialist for a fully site-based role. You will lead complex GMP deviation investigations, drive CAPAs, and partner with Manufacturing, Quality, and Engineering to ensure product quality and regulatory compliance.You will author clear deviation reports, monitor CAPA effectiveness, and participate in...

Senior Deviation Specialist Location: Visp, Switzerland The actual location of this job is in Visp, Switzerland. Join Lonza's Quality organization in Visp and play a critical role in ensuring the quality, compliance, and reliability of life-saving therapies. As a Senior Deviation Specialist, you will lead complex investigations, drive continuous...

pCTC is supporting a global leader in pharmaceuticals in their search for a QA Specialist in the Valais region, Switzerland. This 7-month contract focuses on material receipt services, ensuring GMP compliance, and maintaining accurate raw material data within the LIMS system. /ppYou will collect KPIs, manage deviations and changes, and escalate quality...

ppDie We make it GmbH ist ein national tätiges Unternehmen in der Schweiz, das dank langjähriger erfolgreicher Erfahrung über eine hohe Kompetenz im Bereich der Personaldienstleistungen verfügt. Die Rekrutierungsaktivitäten sind auf die Kernbereiche Industrie, Technik, Büro/Verwaltung, Engineering, Pharma und IT fokussiert. Die We make it GmbH stellt...

Swisslinx AG in Bern is seeking two GMP Compliance Specialists to support deviation management, change control, documentation and risk assessments within a GMP-regulated environment. The roles start on 1 December 2026, run for about seven months, with a workload of 100% (41 hours per week) and possible remote work. Two positions available; ideal candidates...

pAt Consultys Switzerland, we empower Life Sciences innovation. We are offering a permanent opportunity for a Quality Systems Specialist (GMP) to support key quality activities in a regulated environment, contributing to compliance, continuous improvement, and operational excellence within the pharmaceutical, chemical, or food manufacturing industry....

PurposeEmbed onsite QA support into GMP shop-floor operations and automation-related batch quality oversight.Revised responsibilitiesReview batch records and automation-generated batch exceptions, escalating unexplained gaps or discrepancies.Support deviations, root cause, CAPAs, change control and effectiveness checks.Conduct GMP walkdowns and assess...

Quality Assurance Associate III role in Solothurn, Switzerland, focusing on downstream manufacturing and equipment. Responsibilities include reviewing GMP documents, managing deviations, and participating in batch release.

Für ein führendes Pharmaunternehmen in Basel suchen wir einen qualifizierten Laboratory Specialist QC Mikrobiologie (m/w/d) Allgemeine Informationen: Standort:Kaiseraugst Pensum:65%, vor Ort Start:01.01.2027 Dauer:6 Monate mit Option auf Verlängerung Pikett-/Wochenendarbeit: Punktuell Ihre Aufgaben: Eigenständige Bearbeitung und Nachverfolgung von...

pI'm currently supporting a leading biotechnology organisation in Switzerland seeking an experienced bQA Specialist /b to support GMP quality activities at its manufacturing site in Visp. /ph3Key Responsibilities: /h3ulliSupport day-to-day QA operations within a GMP-regulated manufacturing environment. /liliManage deviations, CAPAs, change controls and...

Für ein führendes Pharmaunternehmen in Basel suchen wir einen qualifiziertenAllgemeine Informationen:Pensum: 65%, vor OrtDauer: 6 Monate mit Option auf VerlängerungPikett-/Wochenendarbeit: PunktuellIhre Aufgaben:Eigenständige Bearbeitung und Nachverfolgung von Deviation Reports (DRs) und Assessments in enger Zusammenarbeit mit Quality Assurance und...

Main Responsibilities: Support and consulting in the area of aseptic manufacturing and microbiological laboratories (no performance of activities within manufacturing or the laboratory) Review and ensure compliance with GMP requirements in production Control, review, and documentation of work steps, review of processes in aseptic production. Participation...

RUAG sucht in Luzern/Emmen einen Quality Engineer, der die Produktion bei qualitätsrelevanten Fragestellungen unterstützt und eng mit Manufacturing Engineering, Configuration Management, Produktion, Supply Chain und dem Kunden zusammenarbeitet, um die Produktqualität sicherzustellen.Sie erstellen Qualitätspläne, Prüfanweisungen und Nachweise,...

I'm currently supporting a leading biotechnology organisation in Switzerland seeking an experienced QA Specialist to support GMP quality activities at its manufacturing site in Visp.Key Responsibilities:Support day-to-day QA operations within a GMP-regulated manufacturing environment.Manage deviations, CAPAs, change controls and quality documentation.Review...

ppAdryan is an internationally operating services group. From our offices in The Netherlands and Switzerland, we offer a full range of services for the life sciences industry. We are specialised in the areas of project management, engineering, CQV and compliance. /p h3Key responsibilities: /h3 ul liHolds all quality related responsibilities for daily...

Acino Pharma AG in Liesberg sucht einen Betriebsingenieur (100%) zur Unterstützung der Solida-Produktion und Verpackung. Sie optimieren Prozesse, sichern GMP-konformen Betrieb und leiten kleinere Investitionsvorhaben.Sie arbeiten eng mit Produktion, Qualität, Instandhaltung und externen Dienstleistern zusammen. Sie bringen ein abgeschlossenes...

pRoche sucht einen GMP-Experten (m/w/d) im Kalibrier-Team am Standort Basel. Sie fungieren als zentrale Schnittstelle für klare, audit-sichere Dokumentation, erstellen SOPs, Arbeitsanweisungen und technische Dokumente und pflegen Stammdaten in CCMS und SAP. /ppSie unterstützen Deviations- und Change-Management, RCA und FMEA und arbeiten eng mit...

pbStart date: /b 1 December 2026, or 1 January 2027 at the latest /ph3About the Role /h3pWe are recruiting a bLogistics Warehouse Compliance Specialist /b for a contract assignment with our client in the pharmaceutical industry. /ppYou will support bGxP compliance across logistics and warehouse operations in Basel and Kaiseraugst /b, including a global...

h3About Us /h3pten23 health is a human-centric and sustainable strategic partner of choice for the pharmaceutical industry and biotech start-ups for the development, manufacture, and testing of tomorrow’s medicines. We support our clients in developing differentiated, stable, usable, and safe injectable treatments for patients. /ph3Your mission...