23 Temporär Jobs für Sie gefunden

No sponsorships for non-EU candidates Are you ready for a new challenge? In this interesting role as a Data Technician you are working at a large international technology company. Start: 1st of MarchType of employment: Until end of June (potential to extend to full 18-month contract depending on budget & performance)Location: Zürich onsiteWhat Will Make You Stand Out (ideal qualifications)Datacenter experience What We’re Looking For (minimum qualifications

TON RÔLE :En tant que membre de l'équipe QC Projet & Equipement, tu participeras à la mise en place de nouveaux équipements, en suivant les flux de qualification interne (IQ,OQ,PQ). Ces qualifications incluent une partie importante de CSV, pour garantir le respect de la data integrity.Ton rôle est de conduire notre évolution vers une automatisation accrue et un laboratoire de pointe par la qualification et la validation de nouveaux équipements et systèmes

Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart Date: 01.03.2025End Date: 27.02.2026 On that role, you will ensure compliance with electronic data integrity (e-DI) processes in QC laboratories and Manufacturing. This includes performing QA oversight, reviewing audit trails, approving CSV/Qualification documents for equipment (e.g., HPLC, GC, MES), and defining critical data flows to maintain QA integrity. You will

On behalf of our client, an international pharma company based in canton Zug, we are seeking a Senior PV Scientist.This role is fully remote (from Switzerland).In this role, you will serve as a global product lead for Pharmacovigilance activities within the Safety department including managing PV Scientist(s) assigned to products within the Senior PV Scientist's designated products. General Information: Contract type: temporary contract via RandstadStart d

CSV Engineer (m/f/d)Location: Stein, SwitzerlandCompany: LonzaEmployment Type: Full-TimeJoin Lonza, a global leader in life sciences, and contribute to impactful pharmaceutical projects. We are seeking a CSV Engineer to support the commissioning, qualification, and validation (CQV) activities of cutting-edge systems in Stein, Switzerland. ResponsibilitiesOversee and execute CSV deliverables and tests for Delta V software development, ensuring compliance wi

Reportingto the 'Analytical Development& Innovation Lab Manager'in the Global Analytical Development organization, this role represents anopportunity to significantly contribute to the high-tech analyticallaboratories in the BDC, by conducting analytical testing, data evaluation and reporting, toensure the delivery of our specialty innovator Biotech pipeline to patients. Your Role:Conduct routine analytical testing in at least one of the following area

Für unsere Kundin in Schweizer Versicherungsumfeld suchen wir Verstärkung im Rahmen einer Migration.Task:Der auf Entity Framework 1.0 basierende Data Access Layer einer gösseren Anzahl von Services soll auf eine aktuelle Version von EF angehoben werden.Skills:Mehrjährige Erfahrung in der Softwareentwicklung mit .NET Framework (C#) und Entity Framework mit DB-First-Ansatz.Fundierte Kenntnisse in der Arbeit mit alten und neuen Versionen von Entity Framework

On behalf of our client, an international pharma company based in Baar, we are seeking a Aggregate Report PV Scientist.This role is fully remote (from Switzerland).In this role, you will be a part of the Safety Surveillance and Aggregate (SSA) Reports team and you will be responsible for managing the processes for all aggregate reports (PSURs, DSURs, PADERs and local reports).You will work closely with the vendors and the vendor oversight team, and with th

Johnson & Johnson AG is a leader in MedTech.We care for the world... starting with the individual. This guiding principle encourages and unites the people at Johnson & Johnson. The culture of caring is at the heart of our corporate philosophy, which is anchored in our Credo.Do you want to be part of this family?We, Johnson & Johnson AG MedTech, are recruiting for a Digital Customer Service Assistant, located in Zuchwil, Switzerland.In this role, you will b

For our client, Merck Aubonne, we are currently looking for an MSAT DSP Laboratory Technician (6 months).Your main responsibilities:Execution and recording of laboratory experimentsCoordination and collaboration with analytical support teamData collection and interpretation of the experiments' resultsDetection of unexpected eventsContribution to batch records and work instructions creationActively participate to the continuous improvement of processes Your

For one of our clients, an international biotechnology company, we are looking for a Senior Material Planning Analyst.General Information:Start date: ASAPDuration: 12 months contract, with the possibility of extensionWorkplace: Luterbach, SolothurnWorkload: 100%Working hours: StandardAbout the job:The incumbent supports manufacturing planning for Solothurn DS Manufacturing Sites for both clinical and commercial programs. The incumbent collaborates daily wi

In this role your responsibilities will include:Perform routine testing techniques such as the following, with a high degree of reliability, efficiency and accuracy:HPLC/UPLC chromatography-based methodsCapillary electrophoresis based methodsSpectrophotometry based methodsProcess related impurities testing based on ELISA, ddPCROD and TOC Test.Compendials methodsDeliver data treatment and analytical reports of high quality.Contribute to the writing of SOPs

For our client near Lucerne we are looking for a process engineer: Contract: temporary Duration: 1 year Location: close to Lucerne with willingness to travel The contractor will be responsible for:Qualification of surface treatments of metallic alloysQualification of manufacturing processesCreation of Qualification Test Plan and ReportCreation and revision of Process SpecificationsProcess audits, in the field of his expertise, as technical auditor.Educatio

Responsibilities:Lead the implementation of EHS standards and practices throughout the project lifecycle.Collaborate with design teams to ensure safety, environmental, and sustainability aspects are embedded into project designs.Participate in risk assessments, including HAZOP, ATEX, containment, and fire safety evaluations during different project phases (from feasibility to detailed design).Maintain accurate records of basic container data to facilitate

Fachkompetenz• Ausgewiesenes und fortlaufend aktualisiertes Wissen als Oracle-Appliance-Spezialist im Oracle-ODA oder AIX-/EXADATA-Umfeld• Kenntnisse im Tuning von Datenbanken und SQL-Statements• SQL- und PL/SQL-Kenntnisse• Solide Kenntnisse hochverfügbarer Datenbank-Umgebungen• Kenntnisse in der Shell-Programmierung• Erfahrungen in Hochverfügbarkeitstechnologien Oracle Data Guard • Erfahrung im Umgang mit Cloud Control 12c• Kenntnisse Oracle Database Appl

Within the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "DSP Manufacturing Senior Technician " who will support the DSP large-scale operations (GMP and pilot).You will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells. You will support the DSP activities from an operational and documentation point of view: column p

Within the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "USP Senior Technician" who will support the USP large-scale operations (GMP and pilot).You will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells. You will support the USP activities from an operational and documentation point of view: cell expansion, bioreac

We are seeking a Public Affairs Specialist - Senior Manager Rare Disease Corporate Affairs to support public affairs initiatives, policy engagement, and stakeholder communications on behalf of our client in the healthcare sector. The role involves advocacy, government relations, and external communication to ensure alignment with corporate objectives and healthcare policies. The successful candidate will work closely with internal teams, government agencie

Within the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "DSP Manufacturing Associate Scientist " who will support the DSP large-scale operations (GMP and pilot).You will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells. You will support the DSP activities from an operational and documentation point of view: column

An exciting new 6-month opportunity has arisen to join us as Quality Assurance Qualification Expert for our Biotech drug substance plant in Corsier-sur-Vevey.Your role: As an integral member of the Quality Unit, you provide QA expertise for Equipment Qualification/Requalification, Sterilization qualification, Cleaning Validation, Raw Material Qualification, Process & Analytical Validation, and Computerized System Validation.The role consists to elaborate t

Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contract (until 31.12.2025)Start Date: ASAP You care about customers? UCB does as well! As a patient-centric company, UCB is searching for the right fit for their Patient Supply Quality Control department. As an Analytical Transfer & QC Readiness Expert, you will ensure the compliant transfer, validation, and verification of analytical methods while supporting investigations and Ch

Within the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "USP Manufacturing Associate Scientist " who will support the USP large-scale operations (GMP and pilot).You will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells. You will support the USP activities from an operational and documentation point of view: cell e

For our client, a leading international Pharmaceutical company, we are looking for a Quality Manager within IMP Quality Clinical Packaging.General Information:Start date: ASAP; 01.05.2025Latest Start Date: 01.06.2025Duration: 12 months (max till end May)Extension: PossibleWorkplace: Kaiseraugst, AargauWorkload: 100%Remote/Home Office: Possible, min. 80% onsiteDepartment: IMP Quality Operations Basel&Kau (MMQIE)Working hours: StandardAbout the job:IMP Quali