19 English-speaking jobs in Allschwil

We are seeking an experienced communications leader who combines strategic thinking with hands-on execution. In our lean, high-performing team, success requires someone who is equally comfortable shaping strategy and personally creating content, building digital experiences, and developing high-quality branded materials.

Lead AMOS implementation projects in airline or MRO environments. Requires practical business experience, expert AMOS knowledge, and project management skills. Collaborate to embed MRO processes and advise on digital transformation.

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.

Experienced and reliable cleaners needed for part-time permanent contracts. Tasks include home, office, and end-of-tenancy cleaning. Requires cleaning industry experience and German, English, or French skills.

Experienced and reliable Cleaning Agent needed for part-time contracts. Tasks include home, office, and end-of-tenancy cleaning. Requires cleaning industry experience and German, English, or French language skills.

Support Drug Safety Systems by translating business needs into system solutions, managing reporting, and ensuring compliance. Ideal for early-career professionals with technical aptitude in information systems or data analytics.

Senior Scientific Associate in Analytical Development performs method development, optimization, validation, and stability testing for drug products. Requires 4-10 years of pharmaceutical analytical development experience and knowledge of instrumentation like HPLC.

Manager Technical Product Management to evolve PV technology, focusing on case processing systems and operational excellence. Drive product roadmaps for platforms like ArisGlobal LSMV, ReporterX, XDI, and RxLogix, ensuring global compliance.

Senior Scientific Associate in Analytical Development. Responsibilities include method development, optimization, validation, and stability testing for drug products. Requires 4-10 years of pharmaceutical analytical development experience.

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

CPCTS Manager (Artwork Focus) to lead commercial pharmaceutical artwork projects across the product lifecycle. Manage artwork change, coordinate development, and ensure compliance with global regulatory requirements.

Medical Director Endocrinology Europe, MD needed to provide medical and scientific support across Phase 1-4 clinical development. Requires MD/DO with residency and 2+ years in clinical R&D, focusing on protocol design, data interpretation, and regulatory response.

Lead AMOS implementation projects in Airline & MRO environments. Requires practical business experience, expert AMOS knowledge, and project management skills for digital transformation.

Swiss AviationSoftware seeks a Release Manager to lead and evolve end-to-end release management for AMOS, web, mobile, and integrated solutions. The role involves defining and maintaining release strategy, processes, and governance, coordinating release activities across cross-functional teams, and ensuring predictable, efficient, and high-quality software deliveries.

The Clinical Supply Manager is responsible for managing, coordinating, and delivering trial supplies for global clinical trials. This role involves developing supply plans, managing vendor relationships, overseeing packaging and distribution, and ensuring compliance with GMP, GCP, and company regulations.

Lead Manager responsible for managing the complete sales process for aviation software. This role involves driving strategic sales initiatives, coordinating tender responses, and building customer relationships. B2B software sales experience is essential.

Provides strategic regulatory leadership for programs, overseeing all regulatory activities across the product lifecycle. Drives collaboration with cross-functional partners to ensure consideration of regulatory perspectives. Serves as a trusted advisor across the company and may be recognized as an expert externally.

Directs Phase 1-3 clinical trials, develops study protocols, and collaborates with multidisciplinary teams. Responsible for clinical trial program oversight, resource planning, and communication with internal and external stakeholders. Requires MS degree in Life Sciences or related field with 10+ years of experience in industry or equivalent combination of education and experience. Expertise in drug development, operations, and strategic planning is essential.

Leads the design and conduct of observational research to support drug development strategies, regulatory approvals, and payer/HTA/provider engagements. Serves as statistical lead and subject matter expert for RWE/HEOR research design, methodologies, and data analysis. Develops study protocols, statistical analysis plans, and study reports. Collaborates with internal and external stakeholders to ensure project timelines and goals are met.