19 English-speaking jobs in Allschwil

QC Specialist needed for bioindicator production and testing. Responsibilities include microbiological quality controls, raw material management, and documentation per ISO/GMP guidelines. Microbiology background is essential.

Laboratory Animal Technician EFZ (30-80%) supports studies in animal husbandry at Swiss TPH. This role involves diverse tasks in the central laboratory, contributing to health research under high ethical standards. Weekend and public holiday shifts are required.

Full Stack/All-round Software Engineer to develop in-house tools. Implement solutions from database (PostgreSQL, Oracle) to frontend (Java/Swing, Vaadin/HTML/JavaScript). Requires 2-3 years experience with Java, SQL, and Agile.

Contractor Senior Clinical Trial Manager to manage and execute clinical trial preparation and conduct. Requires 6+ years in biotech, expertise in global trials, and knowledge of ICH-GCP.

Seeking an established Drug Safety Physician with MD and industry experience to lead safety activities across development and post-marketing phases. Responsibilities include pharmacovigilance, signal management, and regulatory safety reporting.

Experienced Product Owner needed for Production Planning in Aircraft Maintenance. Own product vision, roadmap, and backlog, translating customer needs into requirements. Requires strong aviation maintenance knowledge and Agile understanding.

Tender Specialist to strengthen tender capabilities within Abbott’s Established Pharmaceutical Division. This role supports strategy execution, analyzes market data, and collaborates cross-functionally to deliver winning tender strategies.

Oversee clinical research and medical management for Lixudebart in Fibrosis (Hepatology). Requires MD/equivalent, 4+ years in Hepatology, and experience in early/late stage clinical development for liver diseases.

Senior Financial Analyst to lead Abbott EPD financials by running the planning process and generating market insights. Responsibilities include financial data analysis, report preparation, and building financial models. Requires 3-5 years in corporate finance.

Experienced Clinical Development Lead needed to provide scientific leadership across clinical study design, execution, and interpretation. Responsibilities include driving program objectives and leading regulatory documentation. Requires advanced degree and 7+ years in clinical development.

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.

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.

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.

Senior Scientific Associate Location: Allschwil, Basel Area, CH Idorsia Ltd is reaching out for more – We have more ideas, we see more opportunities and we want to help more patients. In order to achieve this, we will develop Idorsia into a leading biopharmaceutical company, with a strong scientific core.

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.

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.

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