63 English-speaking jobs in Canton of Basel-Landschaft

Submissions & Regulatory Intelligence Manager to guide Clinical Data Standards, ensuring consistency across clinical trials and regulatory compliance. This role requires expertise in RHA guidance and industry standards like SDTM/ADaM.

Legal Counsel provides pragmatic, business-oriented legal support for wholesale activities across international purchasing, distribution, and sales. Responsibilities include drafting and negotiating commercial agreements and advising on cross-border trade and compliance.

Quality Engineer Compliance strengthens quality and regulatory compliance in production. Tasks include planning audits, analyzing non-conformities, and applying relevant norms. Requires a technical degree and QA experience in industrial settings.

Lead the MES & PI Competence Center to drive digital transformation. Define strategy, manage roadmaps, and oversee Digital Manufacturing solutions in a regulated environment.

Apprenticeship IT Specialist EFZ 2027 focusing on Application Development. Develop and maintain software for high-tech medical devices, analyzing requirements and creating solutions. Requires good math/science grades and strong logical thinking.

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.

IT Service Delivery Manager to own core ITSM processes globally, leading Incident, Problem, Configuration, and Event Management. Requires 7+ years in IT Operations/Service Management and ITIL Foundation certification.

Own the master data workstream for a new manufacturing facility, defining SAP structures and establishing data governance models. Ensure compliance with GMP and ALCOA integrity.

Lead full lifecycle management of Körber PAS-X MES, supporting new facility startup and digital transformation. Requires 4-6 years of experience in regulated pharma/biotech environments.

Medical Monitor specializing in Pharmacovigilance and Medical Device Safety. Responsibilities include medical oversight of clinical trials, safety signal evaluation, and regulatory support for pharmaceutical and medtech solutions. Requires MD/MBBS and 2+ years of relevant experience.

Legal Counsel provides pragmatic, business-oriented legal support for wholesale operations, drafting and negotiating commercial agreements. Advises on international trade, cross-border sales, and regulatory compliance.

Embedded Software Engineer specializing in C/C++ firmware for ARM microcontrollers in industrial automation. Responsibilities include developing robust firmware, managing industrial communication protocols (OPC UA, Modbus, CANopen), and system testing. Requires 5+ years of experience.

Clinical Data Manager responsible for planning, setup, conduct, cleaning, and closeout of clinical trial databases. Duties include eCRF development, data cleaning using R, and coordinating external data reconciliation.

Director FP&A & Reporting drives strategic business planning, performance management, and financial insights for executive teams. This role manages forecasting, data models, and supports M&A activities within a global life sciences company.

Drive growth for Industrial Testing through market development and strategic customer engagement. Identify new opportunities, shape market strategies, and act as the technical and commercial expert for Industrial Testing applications.

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.

Senior Scientific Associate for Technical Manufacturing Laboratories. Participate in formulation and process development trials, conduct IPC tests, and manage inventory. Requires 3+ years in pharmaceutical drug product formulation, preferably solid dosage forms.

Medical Sensor Development Internship at a medical device company. Characterize prototypes, draw conclusions from data, and propose strategies to improve sensor performance. Requires a bachelor's or master's degree in a relevant field.

Internship in Sensor Development at a medical device company. Tasks include building sensor prototypes, designing experiments, and analyzing data for transcutaneous monitoring systems. Requires a degree in electrical engineering and experience with 3D printing.