3 jobs found in Luterbach, Solothurn

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    • luterbach, solothurn
    • contract
    Do you want to work in a biotech company? Do you have experience in sample management and aliquoting? You should then read the following lines!Our client, based in Solothurn, is looking for a Laboratory Assistant III for a 4 months mission with possibility of extensionThe main responsibilities include sample pick-up, movement, aliquotation and shipment to the respective testing site as part of the Quality Control Sample Management and Logistics team. Other activities include washing, distribution and autoclave of labware.The Logistics/Sample Management team will ensure the timely transfer of analytical samples from the WIP laboratories to the central laboratory. These samples include in-process samples, equipment validation and other study relevant samples.The Quality organization at the new Solothurn site is envisioned to be supported by team members with diverse backgrounds that are capable of cross functional work to support the high throughput design of the facility. As the site moves through the design phase into operational readiness, Quality staff will be focused on incorporating a new operations strategy into the quality management systems, lab systems and business systems. The operational strategy strongly relies on the incorporation of online real-time monitoring, automation of routine testing wherever possible and integrated information technology systems to bring transparency to routine business operations. As such, experience with electronic batch records and integrated sampling plans would be of advantage.Expected know-how and skills:• Good English language skills. Dual Language of advantage with preferences for German.• Must have basic knowledge of Microbiology and Chemistry.• Good aseptic working skills.• Aliquoting experience.• Strong organizational skills and ability to work autonomously.• Good ability to communicate with all levels of management, peers, contractors and external partners effectively.• Optimally have know-how with Labware and Oracle system. Do not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.
    Do you want to work in a biotech company? Do you have experience in sample management and aliquoting? You should then read the following lines!Our client, based in Solothurn, is looking for a Laboratory Assistant III for a 4 months mission with possibility of extensionThe main responsibilities include sample pick-up, movement, aliquotation and shipment to the respective testing site as part of the Quality Control Sample Management and Logistics team. Other activities include washing, distribution and autoclave of labware.The Logistics/Sample Management team will ensure the timely transfer of analytical samples from the WIP laboratories to the central laboratory. These samples include in-process samples, equipment validation and other study relevant samples.The Quality organization at the new Solothurn site is envisioned to be supported by team members with diverse backgrounds that are capable of cross functional work to support the high throughput design of the facility. As the site moves through the design phase into operational readiness, Quality staff will be focused on incorporating a new operations strategy into the quality management systems, lab systems and business systems. The operational strategy strongly relies on the incorporation of online real-time monitoring, automation of routine testing wherever possible and integrated information technology systems to bring transparency to routine business operations. As such, experience with electronic batch records and integrated sampling plans would be of advantage.Expected know-how and skills:• Good English language skills. Dual Language of advantage with preferences for German.• Must have basic knowledge of Microbiology and Chemistry.• Good aseptic working skills.• Aliquoting experience.• Strong organizational skills and ability to work autonomously.• Good ability to communicate with all levels of management, peers, contractors and external partners effectively.• Optimally have know-how with Labware and Oracle system. Do not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.
    • luterbach, solothurn
    • contract
    For our client, an international biotech company, we are looking for a: Manufacturing Associate Location: SolothurnContract: Temporary  Job Description:The Manufacturing Support Associate will support Manufacturing activities in regards to Compliance, Recipe Management, Documentation, Technology Transfer, and Training. An understanding of the manufacturingprocess and its equipment, current regulations, and cGMP’s are needed to perform this position effectivelyTasks:  MFG Documentation: Initiate and monitor manufacturing documentation including Guides, SOPs, Work Instructions and other document typesRecipe: Coordinates and/or Makes revisions to recipes, both in DCS and MES, including parameters, resource text (RTE text) and resource groupsSupport of the manufacturing process(including on floor support as needed) and represents MFG in cross functional groups. Investigating & Troubleshooting discrepancies on the floor, implementing corrective actionsIdentifies improvement opportunities for MFGSupport scheduling of MFG by ensuring production schedule reflects actual processSupport Training of MFG staff by writing, editing or designing training           materialsSupports small projects by working in cross functional teams to collect data, analyze data, and execute various action items against set timelines. May lead some small projects via cross functional teamsQualifications: An understanding of the manufacturing process and its equipment, current regulations, and cGMP’s are needed to perform this position effectively3 to 5 years experience in GMP Production environment, ideally within Biotech/PharmaBachelor’s degree in Biotechnologies / Pharma or Engineering Degree in Pharma/ Biotechnologies preferred
    For our client, an international biotech company, we are looking for a: Manufacturing Associate Location: SolothurnContract: Temporary  Job Description:The Manufacturing Support Associate will support Manufacturing activities in regards to Compliance, Recipe Management, Documentation, Technology Transfer, and Training. An understanding of the manufacturingprocess and its equipment, current regulations, and cGMP’s are needed to perform this position effectivelyTasks:  MFG Documentation: Initiate and monitor manufacturing documentation including Guides, SOPs, Work Instructions and other document typesRecipe: Coordinates and/or Makes revisions to recipes, both in DCS and MES, including parameters, resource text (RTE text) and resource groupsSupport of the manufacturing process(including on floor support as needed) and represents MFG in cross functional groups. Investigating & Troubleshooting discrepancies on the floor, implementing corrective actionsIdentifies improvement opportunities for MFGSupport scheduling of MFG by ensuring production schedule reflects actual processSupport Training of MFG staff by writing, editing or designing training           materialsSupports small projects by working in cross functional teams to collect data, analyze data, and execute various action items against set timelines. May lead some small projects via cross functional teamsQualifications: An understanding of the manufacturing process and its equipment, current regulations, and cGMP’s are needed to perform this position effectively3 to 5 years experience in GMP Production environment, ideally within Biotech/PharmaBachelor’s degree in Biotechnologies / Pharma or Engineering Degree in Pharma/ Biotechnologies preferred
    • solothurn, solothurn
    • temporary
    Do you have a first GMP experience ? Would you like to work in a multinational environment ? You should then read the following lines!One of our clients, specialised in the Life Sciences industry and based in the Solothurn area, is looking for a Manufacturing Associate - Dispensing for a 1 year contract. The dispensary area is the start of production: the team is responsible for weighing the raw materials (liquids and solids) used for the mixing of Solutions in Manufacturing. They work very closely with the Warehouse together and use a lot of different Systems during the work.Tasks:Performs and documents daily manufacturing operations in a cGMP environment (Dispensary Department) including operation of process equipment, execution of validation protocols, and revising cGMP documentationExecutes manufacturing processing steps in Dispensary and/or manufacturing support activities, monitoring the process & MFG documentationEnsures compliance to cGMP as well as maintaining equipment and facilities. The manufacturing associate is detail-oriented with a strong understanding of automated systems and process controls. Maintains training to the required level and supports other functions on site.Performs troubleshooting/investigation of equipment and process issuesRevises documents as instructed, Capable of equipment and/or process changesActively leads or participates in shift exchanges. Coordinates activities and daily schedules with cross-functional areas.Profile:First experience in a GMP environmentFirst experience in a production environmentFluent in English (B2 min.) PLEASE NOTE: the position requires working in 2 shiftsDo those lines trigger your curiosity ? Apply now and let’s chat!  
    Do you have a first GMP experience ? Would you like to work in a multinational environment ? You should then read the following lines!One of our clients, specialised in the Life Sciences industry and based in the Solothurn area, is looking for a Manufacturing Associate - Dispensing for a 1 year contract. The dispensary area is the start of production: the team is responsible for weighing the raw materials (liquids and solids) used for the mixing of Solutions in Manufacturing. They work very closely with the Warehouse together and use a lot of different Systems during the work.Tasks:Performs and documents daily manufacturing operations in a cGMP environment (Dispensary Department) including operation of process equipment, execution of validation protocols, and revising cGMP documentationExecutes manufacturing processing steps in Dispensary and/or manufacturing support activities, monitoring the process & MFG documentationEnsures compliance to cGMP as well as maintaining equipment and facilities. The manufacturing associate is detail-oriented with a strong understanding of automated systems and process controls. Maintains training to the required level and supports other functions on site.Performs troubleshooting/investigation of equipment and process issuesRevises documents as instructed, Capable of equipment and/or process changesActively leads or participates in shift exchanges. Coordinates activities and daily schedules with cross-functional areas.Profile:First experience in a GMP environmentFirst experience in a production environmentFluent in English (B2 min.) PLEASE NOTE: the position requires working in 2 shiftsDo those lines trigger your curiosity ? Apply now and let’s chat!  

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