Jobs für gmp documents bei Basel

Bachem Holding AG in Bubendorf sucht eine/n Project Document Manager Lead (PCM) mit Schwerpunkt Dokumentenmanagement im GMP/GxP-Umfeld. Sie verantworten Aufbau, Pflege und Governance des projektweiten DMS sowie Standards, Templates und Freigabeprozesse.Sie führen interne und externe Mitarbeitende, koordinieren Audits, Reporting und Change-Management....

Bachem AG in Bubendorf sucht eine/n Project Document Manager Lead in der Global Engineering Abteilung. Sie bauen das projektweite DMS auf, definieren Standards und steuern Workflows, um eine revisionssichere Dokumentation über alle Phasen sicherzustellen.Sie führen Teams, koordinieren interne/externe Mitarbeitende, unterstützen PMO-Berichte, Audits und...

GXP CONSULTING Switzerland seeks a Technical Writer with GMP experience to turn complex manufacturing processes into clear, compliant, inspection-ready documentation. You will author, revise and own GMP documents for aseptic manufacturing, including SOPs and work instructions, collaborating with Engineering, Manufacturing, Quality and Compliance.The role...

Um unser kontinuierliches organisches Wachstum voranzutreiben, suchen wir ständig nach hochqualifizierten Fachkräften. Zur Verstärkung unseres Teams in der Global Engineering Abteilung suchen wir eine/n engagierte/n Project Document Manager (PCM) Lead (a), 100%. Ihre Aufgaben Aufbau, Pflege und Steuerung des projektweiten Dokumentenmanagementsystems...

Um unser kontinuierliches organisches Wachstum voranzutreiben, suchen wir ständig nach hochqualifizierten Fachkräften. Zur Verstärkung unseres Teams in der Global Engineering Abteilung suchen wir eine/n engagierte/n Project Document Manager (PCM) Lead (a), 100%.Ihre Aufgaben:Aufbau, Pflege und Steuerung des projektweiten Dokumentenmanagementsystems (DMS)...

Um unser kontinuierliches organisches Wachstum voranzutreiben, suchen wir ständig nach hochqualifizierten Fachkräften. Zur Verstärkung unseres Teams in der Global Engineering Abteilung suchen wir eine/n engagierte/n Project Document Manager (PCM) Lead (a), 100%. Ihre Aufgaben: Aufbau, Pflege und Steuerung des projektweiten Dokumentenmanagementsystems...

Bachem in Bubendorf sucht eine/n Project Document Manager Lead, um das DMS projektweit zu steuern und GMP/GxP-Standards sicherzustellen. Sie führen interne/externe Mitarbeitende, definieren Dokumentationsprozesse und unterstützen das PMO.Sie bringen mehrjährige Erfahrung im Dokumentenmanagement in der Pharma/Biotech-Branche mit, arbeiten detailgenau und...

Senior QA Expert for QC – 7084 URAOur client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a Senior QA Expert for QC The Sr. QA Expert for QC role is a 6M contract with 60% workload. QA responsible for QC oversight to support departmental...

What if your expertise could contribute to work that ultimately makes a difference for patients? Are you looking for an environment where collaboration, expertise, and meaningful challenges come together? Would you value the opportunity to work alongside experienced life-science professionals and contribute to projects across the industry? YES? So let's...

The actual location of this job is in Basel Stücki, Switzerland. For our successful Drug Product Services (DPS) focused branch located in Basel and Stein, Switzerland, we have exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for the fix-term...

Nous recherchons un Ingénieur qualification DQ/IQ/OQ/PQ (Qualification de Conception, d'Installation, Opérationnelle et de Performance) pour accompagner nos clients industriels et pharmaceutiques dans la qualification de leurs équipements et installations.Rédiger et exécuter les protocoles de qualification DQ, IQ, OQ et PQAnalyser les spécifications...

QA Specialist – 7079Our client, a global pharmaceutical company, is looking for a QA Specialist to support Quality Assurance activities related to Investigational Medicinal Products (IMPs).The role focuses on GMP documentation review, quality system activities, batch documentation, and coordination with Contract Manufacturing Organizations (CMOs). The...

Roche Basel/Kaiseraugst recherche un/une Validation/Qualification Engineer pour les systèmes informatisés (CSV). Vous concevez et validez des qualifications, rédigez des documents (VMP, SOP) et soutenez les audits réglementaires.Vous collaborez avec les partenaires internes et les fournisseurs externes, en assurant la conformité GMP et le respect des...

Discover your exciting role Shape innovative projects in the pharmaceutical industry and take on responsibility in exciting qualification and validation projects within a dynamic environment at Exyte. Explore your tasks and responsibilities Preparation of qualification and validation plans Preparation and review of specifications, risk analyses, design...

Commissioning, Qualification & Validation Professionals – SwitzerlandKinetics Process Consulting GmbH Vacant since : 22.07.2026 Number of jobs : 5 4000 Basel (BS) 100% By agreement Permanent Registration requirement Location: Switzerland – project locations may include Basel, Visp and other major pharmaceutical manufacturing hubsEmployment Type:...

GXP CONSULTING Switzerland is a Swiss company made up of a passionate team of life-science professionals. Since 2014, we have been providing our clients with cutting-edge expertise and support covering the entire product life cycle. Join a team where your skills will have a real impact on patients’ lives. We are looking for an Engineering Project Manager...

Contract Type: Temporary Fixed-Term Contract (2-Year Assignment / 100%)Your ResponsibilitiesDocumentation & Batch Review: Perform initial intake and completeness checks of manufacturing and packaging records for investigational medicinal products (IMPs), compiling all required documentation packages to support QA batch release.Quality Event Management: Log,...

Discover your exciting role Whether working on engineering or GMP compliance projects, you will contribute to the design and delivery of Clean Utilities systems for clients in the pharmaceutical and biotechnology industries. From concept development through detailed design and project execution, you will support project teams in delivering high-quality...

Whether working on engineering or GMP compliance projects, you will take a leading role in the design and delivery of Clean Utilities systems for clients in the pharmaceutical and biotechnology industries. From concept development through detailed design and project execution, you will provide technical leadership, coordinate project teams, and ensure...

CTC Resourcing Solutions seeks a Technical Testing Lab Assistant for our client in Basel, Switzerland. The role focuses on preparing dental materials for testing and supporting mechanical and material property evaluations in a GMP/regulated lab.You will document results, maintain organized archives for traceability, and assist with calibration and equipment...