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Global Clinical Order Manager: Clinical Supply chain/GMP/CAPA/Masterdata Deployment/Veeva/ERP system/German/English Background: As part of PTDS Global Clinical Supply Chain Management, the Production Enablement function ensures that packaging operations can produce material required by Roche's clinical trials seamlessly, on-time, and while optimizing cost/quality. Within Production Enablement the Global Clinical Order Management team is responsible for preparing any kind of packaging orders that will be produced at our clinical packaging facilities in Kaiseraugst and South San Francisco. The... more ->
S enior Principal Scientist, TechOps (CMC Science) - Recombinant This role is Global and can be based in Bern, CH, Marburg DE, King od Prussia, PA USA or Kankakee IL USA Job Purpose The Senior Principal Scientist is a recognized technical expert within the Recombinant Integrated Product Team (IPT), providing advanced scientific expertise and leading complex technical activities to support product lifecycle management. The role contributes to the execution of product strategies by delivering high-quality scientific input, leading defined technical initiatives, and supporting cross-functional... more ->
CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. As Principal Biostatistician you will provide high level expertise in the specialist area of Research Biostatistics. You will support research activities in alignment with the respective Therapeutic Area (TA) Research Strategies. In... more ->
Principal Scientist, Tech Ops (Tech Transfer and Outsourcing) R-275563 Fullltime/Permanent/CF Level 7 Locations available: Bern Position Description Summary? Lead and oversee technology transfer activities for processes and/or QC analytical methods, including transfer between development, manufacturing, and external partner laboratories. Define and execute transfer strategies, protocols, acceptance criteria, and readiness assessments to ensure successful implementation at receiving sites. Serve as the primary technical point of contact for external partners, including CDMOs and contract... more ->
Researches and develops new medicines for unmet medical needs through innovative medical science from inception, through clinical trials to commercialization. Assesses, monitors and ensures products meet clinical safety standards. Conducts sophisticated analysis, manages research information systems and technical documentation. May be involved in providing para-professional laboratory support for product testing after collection. Establishes relationship with regulatory authorities to establish and maintain registration licenses to sell products globally.? Designs and implements business... more ->
Position Description Summary? Researches and develops new medicines for unmet medical needs through innovative medical science from inception, through clinical trials to commercialization. Assesses, monitors and ensures products meet clinical safety standards. Conducts sophisticated analysis, manages research information systems and technical documentation. May be involved in providing para-professional laboratory support for product testing after collection. Establishes relationship with regulatory authorities to establish and maintain registration licenses to sell products globally.? ?... more ->
Global Product Leader Some roles exist to manage processes. This one exists to make consequential decisions about medicines that matter to patients with serious diseases - and to ensure those decisions are made well, at pace, and with the full weight of evidence behind them. CSL Behring is seeking a Global Product Leader (GPL) to take end-to-end ownership of a late-stage development asset, from late research transition through development, commercialization, and lifecycle management. The accountability is real: for strategy, for delivery, and for the value the asset creates across its... more ->
The Analytical Strategy Director is a key scientific and strategic leadership role. In this position you will be responsible for developing and driving analytical strategies that support drug discovery, development, and regulatory approval. The position ensures the implementation of robust, compliant, and innovative analytical approaches across preclinical and clinical development programs, as well as throughout product life cycle management (LCM). Main Responsibilities & Accountabilities? Strategic Leadership? Develop and lead the global analytical strategy aligned with program and corporate... more ->
At CSL, we're committed to delivering life changing therapies with the highest standards of quality, safety, and reliability. We're seeking a Senior Scientist (m/f/x) Continued Process Verification (CPV) Comparability & Statistics to play a critical role in ensuring consistent product quality and robust manufacturing performance across the product lifecycle. This role sits at the intersection of statistics, manufacturing science, and regulatory compliance, applying advanced data analytics to support decision making, process understanding, and continuous improvement in a regulated... more ->
Position Description Summary: The Scientist PK is responsible for monitoring of non-clinical PK/TK studies conducted internally and externally both in a GLP and non-GLP environment and support modelling activities Main Responsibilities: Design, oversee, and interpret nonclinical PK/QSP studies (GLP and non-GLP) to support regulatory submissions and drug development. Conduct PK, PBPK, QSP modelling and/or work with external collaborators. Prepare and review regulatory nonclinical submission documents. Collaborate with internal stakeholders including pharmacology, toxicology, clinical,... more ->
Instandhaltungsspezialist (m/w/d) - Automation/Troubleshooting/GMP/2-Schicht/Deutsch Projekt: Für unseren Kunden Roche Diagnostics International AG mit Sitz in Rotkreuz suchen wir einen Instandhaltungsspezialist (m/w/d) Hintergrund: Wir bieten Dir die Chance, Deinen eigenen Fussabdruck in unserer automatisierten Produktion zu hinterlassen. Als Teil unseres hochqualifizierten Production Maintenance Teams unterstützt Du die Fertigungslinien unserer Reinraumproduktion (ISO Klasse 7). Bei Roche handeln wir nach unseren Werten Mut, Leidenschaft und Integrität. Du bist der Dreh- und Angelpunkt für... more ->