72 English-speaking jobs in Canton of Basel-Landschaft

Engineering Manager to lead a team delivering capital projects and engineering solutions for new active ingredient introduction. Responsibilities include managing CAPEX projects, developing scopes, and ensuring design quality. Requires a relevant technical degree and strong stakeholder management skills.

Engineering Manager to lead engineers delivering capital projects and engineering solutions for new active ingredient introduction. This role manages CAPEX from concept to completion, integrating efficiency and sustainability.

Drive strategic growth for the Water & Wastewater industry by connecting market needs, customer challenges, and innovation. Develop global industry strategy and strengthen the portfolio for flow measurement technologies.

Senior HEOR Manager/COA Strategy Lead to develop and execute strategic COA plans across clinical programs. Responsibilities include guiding clinical teams, leading COA project execution, and analyzing data for regulatory submissions. Requires a Master's or PhD and 5+ years in Health Outcomes Research.

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.

Senior Internal Auditor Finance & Group Reporting will build the Internal Audit function, conducting risk-based audits across financial reporting, consolidation, and governance. Requires 5+ years' experience and IFRS knowledge.

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.

Drive digital growth in Food & Beverage and Water industries. Define 3-5 year strategy, build customer insight, and develop value propositions. Lead execution across Sales, Marketing, and Technology.

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.

Lead robotics transformation at a manufacturing site, driving development and lifecycle management of robotics across various operations. Own the site robotics strategy, define roadmaps, and lead technology scouting in areas like computer vision. Requires 5+ years of industrial robotics implementation experience.

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.

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.

Quality Engineer Compliance will strengthen quality and regulatory compliance in production. Responsibilities include conducting audits, analyzing non-conformities, and applying relevant norms. Requires a technical degree and experience in industrial QA.

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.

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.

Own the global SEO and GEO strategy across traditional search and AI discovery platforms. Build discoverability foundations using structured data, entity frameworks, and semantic relationships. Define technical standards and monitor performance.

Senior Scientific Associate for Solid Dosage Forms Manufacturing. Responsibilities include planning and executing formulation trials, conducting IPC tests, and managing inventory. Requires 3+ years in pharmaceutical drug product formulation and manufacturing process development.

Optimize the Global Learning & Development portfolio, focusing on Management and Leadership & Competency Development. Design, develop, and implement global L&D solutions, managing programs and vendor relationships. Requires 7+ years in L&D and expertise in adult learning.