219 English-speaking jobs in Basel

Analytical Chemist responsible for managing external CDMOs, defining analytical strategies, reviewing data, and authoring documentation. Requires expertise in small molecule chemistry, CDMO management, and technical data review.

As a Senior Quality Lead within Pharma Development Quality, you will design and deliver risk-based Quality Assurance strategies, audits, and conclusions for post-approval products, affiliates, and processes. You will act as a trusted partner to senior business stakeholders, guiding cross-functional collaboration to ensure global quality standards are met.

Research Associate to design, develop, and optimize surface display libraries for protein engineering and biotherapeutic development. Requires experience with epitope surface display technology, molecular biology techniques, and flow cytometry.

Analytical Chemist responsible for managing external CDMOs, defining analytical strategies, reviewing data, and collaborating with process chemists. Requires PhD in Small Molecules/Synthetic Chemistry with CDMO management experience and proficiency in HPLC/MS data review.

Review and approve physico-chemical QC analytical data packages under cGMP, ensuring compliance with SOPs and Good Documentation Practices. Ensure timely tracking and closure of QC testing activities. Coordinate sample lifecycle activities and manage documentation. Support investigations of deviations, OOX events, and CAPAs. Contribute to customer or regulatory audits.

Designs and delivers IRT systems for clinical trials, ensuring patients receive correct study drugs. Analyzes study protocols, translates requirements into system specifications, and oversees implementation. Manages project timelines, prepares reports, and coordinates cross-functional teams. Requires substantial IRT system design experience and strong communication skills.

Senior Manager responsible for strategy, implementation, and lifecycle management of digital Quality Systems. Serves as a liaison between Quality, IT, and business stakeholders, ensuring technology solutions align with business requirements and industry best practices. Leads system implementations, gathers business needs, and drives process optimization. Manages project scope, timeline, and risks, ensuring GxP compliance. Oversees governance and administration of digital quality tools. Requires 7+ years of experience in Quality Systems, project management, and business analysis. Strong understanding of GxP requirements, Quality System Regulations (QSR), and validation practices. Proven experience managing enterprise system implementations (e.g., Veeva Vault, SAP). Experience in business administration for Veeva QMS.

Senior CAPEX Project Engineer to lead scoping, planning, budgeting, and execution of OSD/FG manufacturing upgrades and expansions in GMP environments.

Senior Statistical Methodology Data Scientist will provide expert methodological guidance on study design, analysis, and decision-making. Develop and implement innovative statistical approaches and translate insights into scalable solutions. Support portfolio-level analyses and represent Roche externally through collaborations and publications. Requires a PhD in a quantitative discipline and 2+ years of experience applying advanced statistical methods to biomedical data.

Leads global supply chain strategy and execution across manufacturing, logistics, and distribution networks. Builds systems, partnerships, and organizational clarity to drive simplification, scalability, and operational excellence. Transforms a largely manual supply chain into a system-enabled model. Builds and leads a global supply chain team.

Leads and transforms Lonza's global marketing strategy across all business platforms. Shapes global brand positioning, drives integrated marketing programs, and oversees the full global marketing ecosystem.

Leads global technology strategy and architecture for development and manufacturing operations in a highly regulated life sciences environment. Responsible for digital manufacturing, data & AI, cybersecurity, and scalable growth.

Senior HEOR Manager leads the development and execution of strategic COA plans for products across therapeutic areas. The role involves guiding internal teams on COA selection, leading scientific execution of projects, and ensuring adherence to regulatory requirements. Requires a master's degree in a relevant field and 5+ years of experience in health outcomes research with expertise in COA/PRO methodology.

IT Support Engineer provides Level 2 support for hardware and software issues, manages user accounts in Active Directory and Azure AD, and assists with Windows and Microsoft 365 environments. Troubleshoots network connectivity issues, handles incidents through an ITSM tool, and contributes to maintaining secure IT systems.

Senior HEOR Manager leads the development and execution of strategic COA plans for products across therapeutic areas. The role involves guiding internal teams on COA selection, leading scientific execution of projects, and ensuring adherence to regulatory requirements. Requires a master's degree in a relevant field and 5+ years of experience in health outcomes research with expertise in COA/PRO methodology.

Clinical Development Director to lead and support clinical development strategy for ophthalmology programs, focusing on gene therapy for anterior and posterior segment eye diseases.

Research Associate to join DeepIR initiative focusing on cell engineering and characterization of T-cell receptor (TCR) and peptide-MHC (pHLA) interactions. Will support workflows for TCR discovery, immune cell engineering, and functional characterization of antigen-specific immune responses.

Lead and manage pharmaceutical projects within commercial QC, authoring and reviewing GMP documents. Ensure timely delivery of QC work packages, including close out, authorization, and provision of documents and reports. Act as a single point of contact for assigned projects and represent commercial QC in internal and customer meetings.

Senior HEOR Manager leads the development and execution of strategic COA plans for products across therapeutic areas. The role involves guiding internal teams on COA selection, leading scientific execution of projects, and ensuring adherence to regulatory requirements. Requires a master's degree in a relevant field and 5+ years of experience in health outcomes research with expertise in COA/PRO methodology.

Leads the development of analytical control packages for synthetic molecules, including intermediates and APIs. Requires a Master's or Ph.D. in chemistry or pharmacy and 5+ years of experience in analytical development of synthetic drug substances. Expertise in HPLC, UHPLC, and MS is essential. Strong communication, project management, and collaboration skills are needed. Must be fluent in English.