- Join our team as an Analytical Project Manager and help drive the success of innovative molecules from early-stage development to commercialization!Key Responsibilities:Collaborate with Analytical Leads to streamline processes and support product launches.Track actions and assist senior managers in achieving program objectives through effective project scheduling and coordination.Monitor project progress, analyze key performance indicators (KPIs), and repJoin our team as an Analytical Project Manager and help drive the success of innovative molecules from early-stage development to commercialization!Key Responsibilities:Collaborate with Analytical Leads to streamline processes and support product launches.Track actions and assist senior managers in achieving program objectives through effective project scheduling and coordination.Monitor project progress, analyze key performance indicators (KPIs), and rep
- Are you currently looking for a new project? Have you already gained experience as a project assistant and feel at home there? Then we have an exciting job for you!For our client Feldschlösschen in Rheinfelden we are looking for a:Project Assistant (m/f/d) 100%Your tasks:Supporting the project management (e.g. scheduling, taking minutes)Creation of reports, presentations and project status documentsMaintenance and management of project plans and schedulesOAre you currently looking for a new project? Have you already gained experience as a project assistant and feel at home there? Then we have an exciting job for you!For our client Feldschlösschen in Rheinfelden we are looking for a:Project Assistant (m/f/d) 100%Your tasks:Supporting the project management (e.g. scheduling, taking minutes)Creation of reports, presentations and project status documentsMaintenance and management of project plans and schedulesO
- For our client in Berne we are looking for a CQV Engineer for a pharma/biotech company:Location: Berne Contract: limited contractDuration: 1 year The CQV Engineer is responsible for planning and executing Commissioning & Qualification (C&Q) activities to ensure project milestones are met. Key responsibilities include:Overseeing commissioning and qualification processes to meet project deadlines.Preparing, executing, and obtaining approval for Design QualiFor our client in Berne we are looking for a CQV Engineer for a pharma/biotech company:Location: Berne Contract: limited contractDuration: 1 year The CQV Engineer is responsible for planning and executing Commissioning & Qualification (C&Q) activities to ensure project milestones are met. Key responsibilities include:Overseeing commissioning and qualification processes to meet project deadlines.Preparing, executing, and obtaining approval for Design Quali
- /p//strong///strong///p//p//strong//span lang="EN-US"/Job Title://span///strong//span lang="EN-US"/ Cost Manager//span///p//p//strong//span lang="EN-US"/Job Number://span///strong//span lang="EN-US"/ LONCAP_250403_BW1//span///p//p//span lang="EN-US"/ //span///p//p//strong/Responsibilities://strong///p//ul style="margin-top:0cm;" type="disc"//li//span lang="EN-US"/Develop and manage project cost estimates and control budgets.//span///li//li//span lang=/p//strong///strong///p//p//strong//span lang="EN-US"/Job Title://span///strong//span lang="EN-US"/ Cost Manager//span///p//p//strong//span lang="EN-US"/Job Number://span///strong//span lang="EN-US"/ LONCAP_250403_BW1//span///p//p//span lang="EN-US"/ //span///p//p//strong/Responsibilities://strong///p//ul style="margin-top:0cm;" type="disc"//li//span lang="EN-US"/Develop and manage project cost estimates and control budgets.//span///li//li//span lang=
- A public sector institution in Switzerland, within the IT and Digital Services domain, is currently looking for a Senior Project Manager with expertise in Information Security. The person in this role will manage and drive strategic projects related to security compliance, secure solution development, and access control measures.Requirements – Education and Certifications:? Master’s degree in Information Systems or equivalent? Certified in project or progrA public sector institution in Switzerland, within the IT and Digital Services domain, is currently looking for a Senior Project Manager with expertise in Information Security. The person in this role will manage and drive strategic projects related to security compliance, secure solution development, and access control measures.Requirements – Education and Certifications:? Master’s degree in Information Systems or equivalent? Certified in project or progr
- For an international pharmaceutical company with an office in Bern, we are looking for an IT Service Desk Specialist to provide hands-on technical support and ensure a seamless workplace IT experience. This is a temporary position with a fixed-term contract of one year.Your Responsibilities:Technical Support & Troubleshooting: Provide first-level support for hardware, software, and network issues, ensuring minimal downtime.User Assistance: Help employees wFor an international pharmaceutical company with an office in Bern, we are looking for an IT Service Desk Specialist to provide hands-on technical support and ensure a seamless workplace IT experience. This is a temporary position with a fixed-term contract of one year.Your Responsibilities:Technical Support & Troubleshooting: Provide first-level support for hardware, software, and network issues, ensuring minimal downtime.User Assistance: Help employees w
- Your role:Within the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "Media&Buffer - Technician" who will support the preparation of Media&Buffer at large-scale (GMP).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 Media&Buffer activities from an operational and documentation point of vYour role:Within the Drug Substance Development (DSD) - Manufacturing department, we are looking for a "Media&Buffer - Technician" who will support the preparation of Media&Buffer at large-scale (GMP).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 Media&Buffer activities from an operational and documentation point of v
- We are currently seeking a Microbiologist for one of our clients in Le Locle, Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you. This is an open ended temporary contract via Randstad.Please note this vacancy requires fluency in French and English.Start: ASAP (max 1 month of notice period)Location: Le Locle, on site Your responsibilities:Ensures that adequWe are currently seeking a Microbiologist for one of our clients in Le Locle, Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you. This is an open ended temporary contract via Randstad.Please note this vacancy requires fluency in French and English.Start: ASAP (max 1 month of notice period)Location: Le Locle, on site Your responsibilities:Ensures that adequ
- For our client, an international company based in Baden, we are looking for a Corporate Procurement Specialist (m/f/d).General Information:Location: BadenContract: TemporaryStart Date: ASAPDuration: 1,5 year (extension possible)Working Hours: 100%Type of working: Home office possible 5 days/weekYour responsibilities: Support the development and execution of corporate procurement strategies across multiple domainsSupport IT-related projects (e.g., servicesFor our client, an international company based in Baden, we are looking for a Corporate Procurement Specialist (m/f/d).General Information:Location: BadenContract: TemporaryStart Date: ASAPDuration: 1,5 year (extension possible)Working Hours: 100%Type of working: Home office possible 5 days/weekYour responsibilities: Support the development and execution of corporate procurement strategies across multiple domainsSupport IT-related projects (e.g., services
- An exciting new 6-month opportunity has arisen to join us as Quality Assurance Process Validation for our Biotech drug substance plant in Corsier-sur-Vevey.Your role: Coach and assure quality systems are applied in a consistent mannerApprove Quality Plans and Validation Master Plan and periodic reviewsAssure correct implementation of CCPs and adequate handling of deviations and CAPAs in order to ensure the validated statusAssure that GMP documentation is uAn exciting new 6-month opportunity has arisen to join us as Quality Assurance Process Validation for our Biotech drug substance plant in Corsier-sur-Vevey.Your role: Coach and assure quality systems are applied in a consistent mannerApprove Quality Plans and Validation Master Plan and periodic reviewsAssure correct implementation of CCPs and adequate handling of deviations and CAPAs in order to ensure the validated statusAssure that GMP documentation is u
- 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 pWithin 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
- For our client, an international company based in Zurich, we are looking for a Group Reporting & Consolidation Manager (m/f/d).General Information:Location: ZurichContract: temporaryStart Date: ASAPDuration: 7 months Working Hours: 100%Type of working: on-site, but home office is possibleYour responsibilities: Responsible for high quality sub-consolidated reporting to our HQ in Japan, including identifying and implementing process efficiencies and coordinFor our client, an international company based in Zurich, we are looking for a Group Reporting & Consolidation Manager (m/f/d).General Information:Location: ZurichContract: temporaryStart Date: ASAPDuration: 7 months Working Hours: 100%Type of working: on-site, but home office is possibleYour responsibilities: Responsible for high quality sub-consolidated reporting to our HQ in Japan, including identifying and implementing process efficiencies and coordin
- On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects. Location: Neuchâtel, SwitzerlandContract Duration: 07/04/2025 – 31/05/2025On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects. Location: Neuchâtel, SwitzerlandContract Duration: 07/04/2025 – 31/05/2025
- For our client, a leading international pharmaceutical company, we are seeking a Commercial Operations Director. General Information:Start date: 12.05.2025Duration: 12 monthsWorkplace: ZurichWorkload: 100%Working hours: StandardHome office: Possible Tasks & Responsibilities: Lead commercialization efforts for Qdenga in Central, South-Eastern Europe (CSEE countries: Netherlands; Belgium; Austria, Switzerland, Poland; Czech Republic & Israel etc.) & other EUFor our client, a leading international pharmaceutical company, we are seeking a Commercial Operations Director. General Information:Start date: 12.05.2025Duration: 12 monthsWorkplace: ZurichWorkload: 100%Working hours: StandardHome office: Possible Tasks & Responsibilities: Lead commercialization efforts for Qdenga in Central, South-Eastern Europe (CSEE countries: Netherlands; Belgium; Austria, Switzerland, Poland; Czech Republic & Israel etc.) & other EU
