35 English-speaking jobs in Allschwil

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.

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.

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.

CPCTS Manager to lead commercial pharmaceutical artwork projects across the product lifecycle. Responsibilities include managing artwork change control, coordinating development, and ensuring regulatory compliance. Requires a relevant science degree and 7+ years in pharmaceutical quality functions.

Senior QA Compliance & Auditing Manager ensures GMP/GDP compliance. Responsibilities include leading supplier qualification, managing audits, and overseeing quality documentation. Requires 7+ years in pharmaceutical QA/Compliance.

Expert Medical Writer provides strategic leadership for planning and authoring high-impact clinical and regulatory documents for global marketing applications. Requires 7+ years of pharma/biotech medical writing experience and leadership of junior writers.

Manager, Medical Writing, Immunology supports the Immunology therapeutic area. Responsibilities include preparing clinical documents, leading projects, managing direct reports, and guiding cross-functional teams. Requires 8+ years of pharma/scientific experience.

Senior Documentation Specialist ensures quality and completeness of clinical trial documentation, including sponsor and CRO TMFs. This role provides expert guidance on compliance, conducts quality reviews, and leads inspection-readiness activities.

Senior SAP Business Analyst specializing in Finance (FI/CO) to own SAP Finance processes. Lead requirements, configure solutions, and ensure SOX, GDPR, and GxP compliance. Requires 5-8 years of SAP analysis experience.

Senior Global Medical Director to shape and execute global medical strategy for key assets. Requires MD, PharmD, or PhD with 10+ years in Medical Affairs, supporting product launches and engaging external experts.