We are looking for an experienced Senior Security & System Engineer to operate and maintain PKI and signing environment as part of an operations team responsible for Security services.As an experienced Senior Security & System Engineer, you will be part of an operations team responsible for Security services. You will operate and maintain the PKI and signing environment in accordance with regulatory frameworks and standards, where your experience with PKI
We are looking for an experienced Senior Security & System Engineer to operate and maintain PKI and signing environment as part of an operations team responsible for Security services.As an experienced Senior Security & System Engineer, you will be part of an operations team responsible for Security services. You will operate and maintain the PKI and signing environment in accordance with regulatory frameworks and standards, where your experience with PKI
We are looking for an administrative Assistant (M/F)Our client is looking for a highly organized Administrative Assistant to join its dynamic team. Main Responsibilities:Organize and follow up meetings in collaboration with the Committee ChairManage documentation using specific toolsAct as liaison with relevant internal servicesMonitor files, update dashboards, and follow up on deadlines in coordination with the ChairAssist with editing weekly activity rep
We are looking for an administrative Assistant (M/F)Our client is looking for a highly organized Administrative Assistant to join its dynamic team. Main Responsibilities:Organize and follow up meetings in collaboration with the Committee ChairManage documentation using specific toolsAct as liaison with relevant internal servicesMonitor files, update dashboards, and follow up on deadlines in coordination with the ChairAssist with editing weekly activity rep
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 w
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 w
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 – 31/05/2025
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 – 31/05/2025
On behalf of our client, we are looking for a QS Analyst (Training & Document Control). Contract: Temporary unlimitedLocation: Le LocleHome office: max 1 day per weekAvailability: ASAP or with maximum 1-month noticeLanguages: French and English fluency requiredResponsibilities:Manage and maintain the electronic training system (assignment, data entry)Support the maintenance of the document control systemManage circulation of documents for approvalReview el
On behalf of our client, we are looking for a QS Analyst (Training & Document Control). Contract: Temporary unlimitedLocation: Le LocleHome office: max 1 day per weekAvailability: ASAP or with maximum 1-month noticeLanguages: French and English fluency requiredResponsibilities:Manage and maintain the electronic training system (assignment, data entry)Support the maintenance of the document control systemManage circulation of documents for approvalReview el
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 Quali
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 Quali
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 u
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 u
For our client, a leading international pharmaceutical company, we are seeking a Clinical Supplies Quality Specialist.General Information:Start date: ASAP, 01.05.2025Duration: until 31.12.2025 with the possibility of extensionWorkplace: Schachen, LucerneWorkload: 100%Working hours: StandardHome office: Possible, 2 days on-site, 3 days home office About the job: The Clinical Supplies Quality team is responsible for release of the packaged and labeled drugs
For our client, a leading international pharmaceutical company, we are seeking a Clinical Supplies Quality Specialist.General Information:Start date: ASAP, 01.05.2025Duration: until 31.12.2025 with the possibility of extensionWorkplace: Schachen, LucerneWorkload: 100%Working hours: StandardHome office: Possible, 2 days on-site, 3 days home office About the job: The Clinical Supplies Quality team is responsible for release of the packaged and labeled drugs
For our client, an international pharma company in Neuchatel, we are looking for a Synergie Production Operator. Your mission will be to carry out certain activities related to the manufacturing process of an active pharamaceutical substance.General information: Start date: ASAPContract: temporary via RandstadEnd date: 27/02/2026Extension: to be clarifiedWorkplace: NeuchatelWorkload: 100%Shift work: yes, 2x8 shiftTasks and responsibilities: Comply with cGM
For our client, an international pharma company in Neuchatel, we are looking for a Synergie Production Operator. Your mission will be to carry out certain activities related to the manufacturing process of an active pharamaceutical substance.General information: Start date: ASAPContract: temporary via RandstadEnd date: 27/02/2026Extension: to be clarifiedWorkplace: NeuchatelWorkload: 100%Shift work: yes, 2x8 shiftTasks and responsibilities: Comply with cGM
For our client, an international company based in Turgi, we are looking for a Project Manager (m/f/d).General Information:Location: TurgiContract: TemporaryStart Date: ASAPDuration: 1 year, with the possibility of extension Working Hours: 100%Type of working: Hybrid (up to 3 days per week Home-Office)Your responsibilities: Taking over commercial and technical responsibility for projects – and proper structuring, planning, budgeting, and processing thereof
For our client, an international company based in Turgi, we are looking for a Project Manager (m/f/d).General Information:Location: TurgiContract: TemporaryStart Date: ASAPDuration: 1 year, with the possibility of extension Working Hours: 100%Type of working: Hybrid (up to 3 days per week Home-Office)Your responsibilities: Taking over commercial and technical responsibility for projects – and proper structuring, planning, budgeting, and processing thereof
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 adequ
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 adequ
On behalf of our client, we are looking for a Trade Compliance Specialist who will be responsible for Sanctioned Country due diligence, Denied Party Screening, import/export tariff code determination, and supporting the team and manager to ensure compliance with customs and other government agency regulations. The role will also support trade-sanctioned country management and acquisition-related projects. The selected candidate will contribute to complianc
On behalf of our client, we are looking for a Trade Compliance Specialist who will be responsible for Sanctioned Country due diligence, Denied Party Screening, import/export tariff code determination, and supporting the team and manager to ensure compliance with customs and other government agency regulations. The role will also support trade-sanctioned country management and acquisition-related projects. The selected candidate will contribute to complianc
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