72 English-speaking jobs in Canton of Basel-Landschaft

Chemist / Conjugation Expert to lead development, optimization, and scale-up of bioconjugation processes for antibody therapeutics. Requires PhD and 5+ years in bioconjugation, process development, or CMC.

Senior Director, Clinical Development Oncology provides medical leadership for clinical programs. Responsibilities include strategy, trial design/execution, safety oversight, and regulatory support. Requires MD or equivalent, oncology experience, and 8+ years in clinical drug development.

Senior Clinical Trial Leader Oncology manages complex global clinical trials, acting as the primary lead for external vendors and partners. Responsibilities include overseeing trial execution, regulatory submissions, and ensuring compliance with GCP. Requires 8+ years of clinical study management experience.

The CMC Program Lead supports CMC strategy execution for pipeline products, overseeing outsourced development from cell line to drug product. This role manages timelines, budgets, and ensures GMP compliance while preparing regulatory CMC documentation.

mAb Technical Lead provides technical oversight of late-phase monoclonal antibody manufacturing by CDMO partners. This role manages manufacturing, testing, and supply to ensure timely clinical supply. Requires a PhD and 5+ years in biologics manufacturing and CMC.

CMC Operation Manager and Regulatory Affairs Support role at Viatris. This position supports global healthcare operations, bridging generics and brands to address worldwide healthcare needs.

PhD Student in Bioprocess Technology focusing on downstream purification of biologics. Design, build, and automate unit operations using pump, filtration, and sensor technology. Requires MSc in a relevant engineering/science field and hands-on experience.

PhD Student in Bioprocess Technology focusing on antibody and viral vector production. Responsibilities include designing, building, and automating cell culture setups, developing upstream processes, and running mammalian cell cultivations. Requires an MSc and technical experience.

0 title: Manager RAC (Regulatory Affairs and CMC) (m/w/d) Manager RAC (Regulatory Affairs and CMC) (m/w/d) We are offering a new challenge as Manager RAC (Regulatory Affairs & CMC) at our site in , Switzerland. You will be a member of the corporate RAC and part of local Swiss regulatory affairs and CMC team dedicated to Drug Substance Business Unit.

Manage congresses, trade shows, and customer events while coordinating end-to-end public and private tender management. Requires 3-5 years in event/project management within MedTech or Life Sciences.

Lead end-to-end product launch excellence for the Gastroenterology portfolio. Develop distributor marketing strategies to accelerate market adoption and international growth. Requires 5+ years in product marketing within MedTech or Diagnostics.

Provides strategic regulatory leadership across the product lifecycle, overseeing all regulatory activities. Key member of the Regulatory Strategy Leadership Team, driving execution for complex programs. Requires 17+ years of biopharma/regulatory experience with ex-US CTA experience.

Develop strategic plans as the statistical lead for Real World Evidence (RWE) strategies. Serve as the analytical methodology expert, designing and executing RWE studies across various data types to support development and regulatory needs.

Develop overall Clinical Pharmacology scientific strategies and oversee pharmacokinetic/pharmacodynamic activities for clinical development compounds. Requires advanced degrees and extensive drug development experience.

Lead end-to-end Supply Chain workstream for product and manufacturing transfers. Define transfer supply strategy, manage risk, and drive cross-functional alignment. Requires 8+ years in Supply Chain or Tech Transfers.

Manager Finance and Controlling responsible for financial accounting, budgeting, forecasting, and financial planning for two organizations. This role requires hands-on experience with Swiss accounting standards and strong analytical skills.

Senior Director, Global Managed Access Programs, Strategy & Operations leads global MAP execution for Neurocrine. This role develops strategy, oversees cross-functional execution, and manages external partners for patient access outside traditional commercial channels.

Drive regional scientific and public health strategy across EMEA. Lead scientific narrative development, public health advocacy, and professional engagement. Requires 5-7 years in scientific affairs or similar regulated healthcare environment.

Develop data-driven solutions for Digital Manufacturing using PI Historian and advanced analytics. Enhance reporting, deepen process understanding, and support investigations across the production lifecycle. Requires technical skills in Python/SQL and manufacturing data experience.

Engineering Manager to lead engineers delivering capital projects for new active ingredient introduction. This role translates molecule development into scalable production assets, managing CAPEX from concept to completion.