NetTemps

Project Manager - Medical Devices, Pharma QA long term contract opportunity for our Basel based client in the Pharma sector. Your tasks: Lead and support global TRD project teams on quality-related topics, questions and issues Develop project quality strategies in alignment with TRD and cross-functional stakeholders Provide quality oversight for assigned development projects, including scientific and technical guidance Prepare and guide project teams for Mock-PAI, PAI and submission readiness activities Support quality agreements, contract input and amendments with third parties Contribute to...  more ->

S olution Engineer/Expert: Linux Mastery/MedTech/Distribution Engineering/Debian Packaging/Make/CMake/Docker/Kubernetes/CI/CD/English/German Projekt: For our client, a major pharmaceutical company based in Rotkreuz, we are looking for a Solution Engineer Background: The Opportunity: Build the Foundation for Life-Saving Technology! Are you driven by a deep need to understand how systems work, from the Kernel to the application layer? Do you see a working system not as an endpoint, but as a baseline for improvement, optimization, and hardening? We are a specialized team of software and hardware...  more ->

Construction Manager: EMSR/Automationsanlagen/Baustellensicherheit/GMP/Normen NIN/NIV/Projektmanagement/Elektroinstallationsbereich/Deutsch/English Hintergrund: Als Mitarbeiter im Kreis "Construction Site Services" sind Sie im Bereich "Operate and Maintain Assets" des Standortes Basel/Kaiseraugst tätig. Der Bereich Operate and Maintain Assets der Roche Pharma am Standort Basel/Kaiseraugst hat den Sinn und Zweck "We do asset care - für einen reibungslosen Betrieb von Areal, Gebäuden und Anlagen" Als Mitarbeiter im Kreis Construction Site Services arbeiten Sie in einem Team von dreizehn Kolleg:...  more ->

Network Supply Manager: ERP (S4Hana)/Supply Chain Planning systems/APICS/JMT/Drug Product/Contract Manufacturing Organizations (CMO)/Drug Substance/English/German Background: The Global Supply Chain Operations Organization seamlessly connects markets to the global manufacturing network by centrally managing supply, inventory and replenishment planning for drug products and drug substances. We orchestrate the value streams between sites and affiliates by balancing the demand and supply equations across markets, products, manufacturing assets and inventory points. We ensure right first-time...  more ->

Responsibilities : Plan, direct, and monitor regulatory affairs activities so the organization has the permits, licenses, certificates, authorizations, and other approvals needed to conduct current and future business activities; and produce, sell, and distribute its goods and services. Support development of consistent roles and work processes. Oversee development of plans, cost estimates, and schedules. Acquire the necessary permits and approvals. Monitor regulatory developments and advise management on the potential impact of regulations on the organization. Establish and maintain positive...  more ->

Responsibilities: Develop global regulatory CMC strategies for enterprise-wide CAPEX and compliance projects through collaboration with functional leaders in Global Regulatory Affairs CMC, Global Regulatory Affairs, R&D, Quality, Global Operations, and other business functions. Assess and facilitate the use of digital innovation for Global Regulatory Affairs CMC, including AI/ML applications that manage or support regulatory submission, notification, assessment and intelligence activities. Collaborate with Procurement, IT, external vendors, and R&D Global Regulatory Affairs to implement...  more ->

Associate Director, Analytical Strategy (m/f/x) The Associate Director, Analytical Strategy will lead the development and execution of analytical strategies to support biopharmaceutical development programs. This role requires deep molecular knowledge, expertise in analytical testing and molecule characterization, and a strong understanding of Quality by Design (QbD) principles and regulatory requirements. The successful candidate will drive analytical decision-making, ensure robust characterization of molecules, and support regulatory submissions with scientific rigor. Main Responsibilities...  more ->

We are currently looking for a Senior Laboratory Specialist to join our team in St. Gallen. Your main responsibilities will include the independent execution and documentation of syntheses and analytical tests; process development and production support for existing and new products; qualification and maintenance of laboratory equipment; compliance with technical, organizational and staff safety measures etc. Key Tasks Independent synthesis, characterization and documentation of synthetic compounds (eg. complex iron compounds, ) in lab and pilot scale Performing analytical method development...  more ->

We are currently looking for an experienced analytical science professional specializing in analytical method validation and transfer to contract manufacturing organizations (CMOs/CDMOs). Strong focus on troubleshooting, root-cause investigation, and ensuring robust analytical performance across external laboratories and CMOs under GMP conditions. In this position you will be directly reporting to the CMC Strategy and Technology Transfer Lead. Key Responsibilities Lead and coordinate analytical method transfer activities to or between Quality Control laboratories and external contract...  more ->