12 clinical Jobs für dich gefunden.

For our client, a dynamic international biotechnology company focused on clinical-stage development, we recruit a:Senior/Executive Medical Director - Clinical

Für einen unserer Kunden, ein internationales pharmazeutisches Unternehmen, suchen wir eine/n Clinical Packaging Technician/Operator.Allgemeine Informationen:Startdatum: 18.05.2026Enddatum: 17.05.2028Arbeitsort: Schachen, LuzernHomeoffice: Nein, 100% vor Ort (Onsite)Arbeitspensum: 100%Arbeitszeiten: StandardÜber die Tätigkeit:Die Organisation Global Clinical Supply (GCS) ist für das End-to-End-Management klinischer Studien verantwortlich. GCS überwacht

Johnson & Johnson MedTech is the world leader in the electrophysiology market: the diagnostic and treatment by catheter ablation of cardiac arrythmias. Our growth has enabled a relentless focus on talent development by providing many new opportunities for our employees to expand their knowledge and develop their careers. Our commitment to developing our leaders is unwavering and our investment in people, technology, and innovation make us one of the best

Position Snapshot Location: Vers-chez-les-Blanc, SwitzerlandEntity: Clinical Research Unit, Nestlé ResearchWork rate: 100%Contract type: TemporaryDuration: 12 monthsSummaryThe Senior Clinical Trial Assistant (Sr. CTA) provides high-quality operational and administrative support to clinical trial teams throughout all phases of a pharmaceutical study. Operating within a fast-paced, regulated environment, the Sr. CTA ensures clinical documentation is

We are currently looking a Senior Technician USP for a 6-month assignment for our client based in Coreir-sur-Vevey. Your roleAs a Senior Technician in Clinical Manufacturing, you will play a key role in supporting large-scale biomanufacturing operations and contributing to the development of innovative biotechnological processes.Your main responsibilities will include:Supporting the scale-up of purification processes from 200L to 2000L for pre-clinical

For one of our clients, an international pharmaceutical company, we are seeking a GMP Documentation Specialist.General Information:Start date: 01.07.2026End Date: 30.06.2027Workplace: Schachen, LuzernHome office: No, 100% onsiteWorkload: 100%Working hours: StandardAbout the work:The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+

Strategic Business Development & In-Licensing Specialist - 100%Starting date : ASAP Location : GenevaType of role : Permanent role Your ResponsibilitiesGenerate high-level scientific and commercial intelligence on potential licensors and therapeutic target areas.Manage business intelligence tools and databases (e.g., IMS, Evaluate Pharma) to support data-driven decision-making.Actively source, evaluate, and execute prioritized in-licensing

Senior Specialist / QA Manager (CMO Operations – Small Molecules)Location: Morges, Switzerland (Up to 2 days of remote work per week) Contract Type: Temporary – Starting ASAP (possibility of extension)Language: Fluent English (C1) required Due to a significant increase in our client activities, we are looking for a Senior Specialist or QA Manager to reinforce a dynamic team of 4 people.This role is 100% focused on managing the Contract Manufacturing

For one of our clients, an international pharma company in Basel, we are currently looking for a Quality Control Project Lead.General Information:Start date: ASAPLatest start date: August 2026Planned employment duration: 12 monthsExtension: unlikelyContract: temporary contract via Randstad (employment)Workplace: BaselWorkload: 100%Home Office: up to 40%Working Hours: Standard Tasks & Responsibilities: Work in a modern quality control organization in

Within the Global Drug Product Development function in our new center, we are looking for a highly motivated (senior) technician with practical experience in a chemical, biological or biotech laboratory. She or he will work together with other scientists within the team, as well as analytical scientists, throughout all steps of drug product development. Your role:Reporting to DP Development manager in the Early-Phase Drug Product Development unit, you

For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a CSV Expert (Synthetic Molecule Facility).General Information:Start Date: ASAPLatest possible start date: 01.08.2026Planned Employment Duration: 12 months with the possibility of extensionWorkplace: BaselHome Office: NoWorkload: 40-60%Team: 10 peopleTraveling: NoDepartment: Basel Site Services Chapter G10 (EFHCAH)Working Hours: StandardAbout the job:The "Synthetic

For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Process Engineer for Biotechnological Production Plants.General Information:Start Date: ASAPLatest possible start date: 01.08.2026Planned Employment Duration: 1 year with the possibility of extensionWorkplace: BaselHome Office: Yes, max 40%Workload: 100%Team: 11 peopleDepartment: DS Large MoleculesWorking Hours: StandardAbout the job:The “Site Network