5 jobs found in Trimbach, Solothurn

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    • luterbach, solothurn
    • contract
    Do you want to work in a biotech company? Do you have experience with protein analytical technologies? You should then read the following lines! Our client, based in Solothurn, is looking for a  Analytical Scientist – Global Manufacturing Sciences for a 1 year contract. ROLE SUMMARY:Based in the Solothurn drug substance (DS) manufacturing facility, the Process Sciences (PS) team within the Global Manufacturing Sciences (GMS) department provides key technical expertise to manufacturing processes at the site. The Analytical Scientist will join the Process Sciences team to support GMS laboratory activities with protein analytical capabilities and expertise. JOB DESCRIPTION:The Analytical Scientist will provide analytical support to small scale cell culture and purification studies in the context of ongoing tech transfer activities, manufacturing investigations and process improvement projects.Prepare and execute laboratory experiments and analyze data.Ensure timely and clear communication of experimental results and potential issues to supervising scientist.Document experimental results in accordance with laboratory procedures and guidelines. QUALIFICATIONS:Bachelor’s or Master’s degree in Biochemistry or Bioprocess Engineering, Chemistry, Biology, or closely allied discipline. 1 to 5 years of industry experience. Solid technical understanding and hands-on experience with protein analytical technologies. Minimum HPLC, UPLC, but iCIEF, CE-SDS and LC-MS desired. Proficiency with automated data workflows and analytics. Good collaboration and communication skills to work within a team. 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 with protein analytical technologies? You should then read the following lines! Our client, based in Solothurn, is looking for a  Analytical Scientist – Global Manufacturing Sciences for a 1 year contract. ROLE SUMMARY:Based in the Solothurn drug substance (DS) manufacturing facility, the Process Sciences (PS) team within the Global Manufacturing Sciences (GMS) department provides key technical expertise to manufacturing processes at the site. The Analytical Scientist will join the Process Sciences team to support GMS laboratory activities with protein analytical capabilities and expertise. JOB DESCRIPTION:The Analytical Scientist will provide analytical support to small scale cell culture and purification studies in the context of ongoing tech transfer activities, manufacturing investigations and process improvement projects.Prepare and execute laboratory experiments and analyze data.Ensure timely and clear communication of experimental results and potential issues to supervising scientist.Document experimental results in accordance with laboratory procedures and guidelines. QUALIFICATIONS:Bachelor’s or Master’s degree in Biochemistry or Bioprocess Engineering, Chemistry, Biology, or closely allied discipline. 1 to 5 years of industry experience. Solid technical understanding and hands-on experience with protein analytical technologies. Minimum HPLC, UPLC, but iCIEF, CE-SDS and LC-MS desired. Proficiency with automated data workflows and analytics. Good collaboration and communication skills to work within a team. 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
    Do you want to work in a biotech company? Do you have experience in purification in GMP environment? You should then read the following lines! Our client, based in Solothurn, is looking for a Manufacturing Scientist Downstream – Global Manufacturing Sciences for a 1 year contract. ROLE SUMMARY:Based in the Solothurn drug substance (DS) manufacturing facility, the Biogen Process Sciences (PS) team within the Global Manufacturing Sciences (GMS) department provides key technical expertise to manufacturing processes at the site. The Manufacturing Scientist will conduct laboratory studies to support tech transfer, manufacturing investigations and process improvement projects. In addition, he/she will support day-to-day laboratory activities as well as the maintenance and improvement of the GMS lab capabilities and procedures. JOB DESCRIPTION:1. Hands on execution and documentation of purification and filtration experiments in the GMS laboratory to support tech transfer, manufacturing investigations and process improvement projects. Analyze lab study samples and data, author reports to document study outcomes, communicate study results to management and project teams. 2. Perform activities to support GMS lab operations including sample and data management, reagents and consumables management, buffer/solution preparation, equipment maintenance, author work instructions and maintain a safe work space. 3. Work within cross-functional teams to support manufacturing scale projects (TT, process investigations, CAPA or change control implementation). Author investigation protocols and reports, validation protocols and reports, sample plans as required. QUALIFICATIONS:Apprenticeship, Bachelor’s or Master’s degree in Bioprocess Engineering, Chemistry, Biology, or closely allied discipline. Apprenticeship with +3 years, BSc. and MSc. with 1 to 5 years of industry experience. Technical knowledge and experience with biomanufacturing and/or process development. Experience in operating lab scale purification and filtration systems. Proficiency with data workflows and analytics is beneficial. Good collaboration and communication skills to work within a team. 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 purification in GMP environment? You should then read the following lines! Our client, based in Solothurn, is looking for a Manufacturing Scientist Downstream – Global Manufacturing Sciences for a 1 year contract. ROLE SUMMARY:Based in the Solothurn drug substance (DS) manufacturing facility, the Biogen Process Sciences (PS) team within the Global Manufacturing Sciences (GMS) department provides key technical expertise to manufacturing processes at the site. The Manufacturing Scientist will conduct laboratory studies to support tech transfer, manufacturing investigations and process improvement projects. In addition, he/she will support day-to-day laboratory activities as well as the maintenance and improvement of the GMS lab capabilities and procedures. JOB DESCRIPTION:1. Hands on execution and documentation of purification and filtration experiments in the GMS laboratory to support tech transfer, manufacturing investigations and process improvement projects. Analyze lab study samples and data, author reports to document study outcomes, communicate study results to management and project teams. 2. Perform activities to support GMS lab operations including sample and data management, reagents and consumables management, buffer/solution preparation, equipment maintenance, author work instructions and maintain a safe work space. 3. Work within cross-functional teams to support manufacturing scale projects (TT, process investigations, CAPA or change control implementation). Author investigation protocols and reports, validation protocols and reports, sample plans as required. QUALIFICATIONS:Apprenticeship, Bachelor’s or Master’s degree in Bioprocess Engineering, Chemistry, Biology, or closely allied discipline. Apprenticeship with +3 years, BSc. and MSc. with 1 to 5 years of industry experience. Technical knowledge and experience with biomanufacturing and/or process development. Experience in operating lab scale purification and filtration systems. Proficiency with data workflows and analytics is beneficial. Good collaboration and communication skills to work within a team. 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
    • temporary
    Randstad Professionals is looking for several Quality Assurance Associate for a major client based in Solothurn. Start date: ASAP, negotiableContract period: 6 - 12 months, extension possible The QA Operations Associate assures that all operations meet or exceed cGMP regulations ensuring the quality Bulk Drug Substance, cell bank supporting on shop floor the daily manufacturing, Warehouse and facility operations. The position needs reactive support of discrepancy identification, resolution on the floor, root cause analysis and corrective action for product and process related non-conformances. The holder will collaborate with product Quality Management for change control. This is accomplished by direct collaboration and oversight of Manufacturing Operations and the review/audit of data and reports as specified by Standard Operating Procedures. This position will support quality key metrics and analysis. This role is expected to be cross-functional between the Manufacturing Site Quality and site organization, and all parts of the quality line organization (QC, Corporate Quality and QA) as well as relevant partner departments. As such, the position is expected to have expert level knowledge in cell culture , purifications process , operations and business processes within a GMP Biotech environment. Previous experience with manufacturing execution systems (Delta V or Syncade) as well as Trackwise, LIMS, electronic documentation and training systems will be an advantage. As the facility is designed to be a high-throughput facility it will also be beneficial to have experience with LEAN, Six Sigma and continuous improvements. If you are interested to take on these responsibilities you should have the following requirements:Must have is expert Level experience in cell culture , purifications process , operations and business processes within a GMP Biotech environment.Dual Language preferred with preferences for German and English.Experience in participating in pharmaceutical technology transfer teamExperience in the qualification of facilities, utilities , equipment and processesMust have strong technical skills and be proficient with typical productivity software (Word, Excel, Powerpoint, Visio, etc.)Candidates with experience in drug substance (or API) and drug product are preferred.Should have proficiencies with the Quality systems and business processes associated with automation and integration of testing and production systems.Demonstrated ability to work autonomously and lead projectGood oral and written communication skills and ability to communicate with all levels of management, peers, contractors and external partners effectivelyDemonstrated problem solving skillsAbility to work in shift model including during the weekendPrior experience with facility construction and start-up is an asset. We can offer you a new challenge in a diverse, innovative and multicultural environment. Have we sparked your interest? Then we look forward to receiving your online application. Please note a Swiss Work permit or EU-citizenship is mandatory for this position.
    Randstad Professionals is looking for several Quality Assurance Associate for a major client based in Solothurn. Start date: ASAP, negotiableContract period: 6 - 12 months, extension possible The QA Operations Associate assures that all operations meet or exceed cGMP regulations ensuring the quality Bulk Drug Substance, cell bank supporting on shop floor the daily manufacturing, Warehouse and facility operations. The position needs reactive support of discrepancy identification, resolution on the floor, root cause analysis and corrective action for product and process related non-conformances. The holder will collaborate with product Quality Management for change control. This is accomplished by direct collaboration and oversight of Manufacturing Operations and the review/audit of data and reports as specified by Standard Operating Procedures. This position will support quality key metrics and analysis. This role is expected to be cross-functional between the Manufacturing Site Quality and site organization, and all parts of the quality line organization (QC, Corporate Quality and QA) as well as relevant partner departments. As such, the position is expected to have expert level knowledge in cell culture , purifications process , operations and business processes within a GMP Biotech environment. Previous experience with manufacturing execution systems (Delta V or Syncade) as well as Trackwise, LIMS, electronic documentation and training systems will be an advantage. As the facility is designed to be a high-throughput facility it will also be beneficial to have experience with LEAN, Six Sigma and continuous improvements. If you are interested to take on these responsibilities you should have the following requirements:Must have is expert Level experience in cell culture , purifications process , operations and business processes within a GMP Biotech environment.Dual Language preferred with preferences for German and English.Experience in participating in pharmaceutical technology transfer teamExperience in the qualification of facilities, utilities , equipment and processesMust have strong technical skills and be proficient with typical productivity software (Word, Excel, Powerpoint, Visio, etc.)Candidates with experience in drug substance (or API) and drug product are preferred.Should have proficiencies with the Quality systems and business processes associated with automation and integration of testing and production systems.Demonstrated ability to work autonomously and lead projectGood oral and written communication skills and ability to communicate with all levels of management, peers, contractors and external partners effectivelyDemonstrated problem solving skillsAbility to work in shift model including during the weekendPrior experience with facility construction and start-up is an asset. We can offer you a new challenge in a diverse, innovative and multicultural environment. Have we sparked your interest? Then we look forward to receiving your online application. Please note a Swiss Work permit or EU-citizenship is mandatory for this position.
    • luterbach, solothurn
    • contract
    Do you want to work in a biotech company? Do you have experience working with bioreactors in GMP environment? You should then read the following lines! Our client, based in Solothurn, is looking for a  Manufacturing Scientist Upstream – Global Manufacturing Sciences for a 1 year contract. ROLE SUMMARY:Based in the Solothurn drug substance (DS) manufacturing facility, the Process Sciences (PS) team within the Global Manufacturing Sciences (GMS) department provides key technical expertise to manufacturing processes at the site. The Manufacturing Scientist will conduct laboratory studies to support Upstream tech transfer, manufacturing investigations and process improvement projects. In addition, he/she will support day-to-day laboratory activities as well as the maintenance and improvement of the MS lab capabilities and procedures. JOB DESCRIPTION:1. Hands on execution and documentation of cell culture experiments in the GMS laboratory to support tech transfer, manufacturing investigations and process improvement projects. Analyze lab study samples and data, author reports to document study outcomes, communicate study results to management and project teams. 2. Perform activities to support GMS lab operations including sample and data management, reagents and consumables management, buffer/solution preparation, equipment maintenance, author work instructions and maintain a safe workspace. 3. Work within cross-functional teams to support manufacturing scale projects (TT, process investigations, CAPA or change control implementation). Author investigation protocols and reports, validation protocols and reports, sample plans as required. QUALIFICATIONS:Apprenticeship, Bachelor’s or Master’s degree in Bioprocess Engineering, Chemistry, Biology, or closely allied discipline. Apprenticeship with +3 years, BSc. and MSc. with 1 to 5 years of industry experience. Technical knowledge and experience with biomanufacturing and focus on mammalian cell culture technology incl. aseptic work techniques and operation of bench scale bioreactors. Proficiency with automated data workflows and analytics. Good collaboration and communication skills to work within a team. 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 working with bioreactors in GMP environment? You should then read the following lines! Our client, based in Solothurn, is looking for a  Manufacturing Scientist Upstream – Global Manufacturing Sciences for a 1 year contract. ROLE SUMMARY:Based in the Solothurn drug substance (DS) manufacturing facility, the Process Sciences (PS) team within the Global Manufacturing Sciences (GMS) department provides key technical expertise to manufacturing processes at the site. The Manufacturing Scientist will conduct laboratory studies to support Upstream tech transfer, manufacturing investigations and process improvement projects. In addition, he/she will support day-to-day laboratory activities as well as the maintenance and improvement of the MS lab capabilities and procedures. JOB DESCRIPTION:1. Hands on execution and documentation of cell culture experiments in the GMS laboratory to support tech transfer, manufacturing investigations and process improvement projects. Analyze lab study samples and data, author reports to document study outcomes, communicate study results to management and project teams. 2. Perform activities to support GMS lab operations including sample and data management, reagents and consumables management, buffer/solution preparation, equipment maintenance, author work instructions and maintain a safe workspace. 3. Work within cross-functional teams to support manufacturing scale projects (TT, process investigations, CAPA or change control implementation). Author investigation protocols and reports, validation protocols and reports, sample plans as required. QUALIFICATIONS:Apprenticeship, Bachelor’s or Master’s degree in Bioprocess Engineering, Chemistry, Biology, or closely allied discipline. Apprenticeship with +3 years, BSc. and MSc. with 1 to 5 years of industry experience. Technical knowledge and experience with biomanufacturing and focus on mammalian cell culture technology incl. aseptic work techniques and operation of bench scale bioreactors. Proficiency with automated data workflows and analytics. Good collaboration and communication skills to work within a team. 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.
    • solothurn, solothurn
    • permanent
    For our client in the heart of Solothurn we are looking for a senior  C/C++ Embedded Engineer.The Team you will be joining has 6 Engineers, 1 technical support engineer and 1 admin support.You will be in the innovation Team responsible for developing new IoT applications for enterprise payment products - cash and cashless.This role is a full time permanent position.Your responsibilities:Hardware near programming in C/C++ on linux for hardware solutionsFull Lifecycle Development of embedded applications for different payment products under consideration of different topics such as; cash out, cardholder verification, contactless payment etc.Product Development and enhancements, bring in new features and ideasElaboration, Design and implementation of automated tests, including the use of HW RobotsWireless connectivity and Cryptography are a big topicTechnical assistance for junior developersClose collaboration with internal stakeholders like sales, application managers etc.Your experience:Fluency in English is a MUSTEITHER a Bachelor's degree in software engineering or computer science, OR relevant technical industry experienceHands-on experience in an embedded software environment with C/C++ on LinuxSome touchpoints and experience in cryptographic topicsExperienced in OOD, OOP and Embedded ARM and RTOS are extremely beneficialExperience with scripting languages such as Bash, Python or elseKnowledge of Wireless communicationKnowledge of Development Tools such as Jenkins, Jira or Git are a huge plusIf you are interested in this opportunity and would like to get to know more about it, please do not hesitate to contact me and send in your application.At this point, we can only consider applications with a valid work permit for Switzerland.
    For our client in the heart of Solothurn we are looking for a senior  C/C++ Embedded Engineer.The Team you will be joining has 6 Engineers, 1 technical support engineer and 1 admin support.You will be in the innovation Team responsible for developing new IoT applications for enterprise payment products - cash and cashless.This role is a full time permanent position.Your responsibilities:Hardware near programming in C/C++ on linux for hardware solutionsFull Lifecycle Development of embedded applications for different payment products under consideration of different topics such as; cash out, cardholder verification, contactless payment etc.Product Development and enhancements, bring in new features and ideasElaboration, Design and implementation of automated tests, including the use of HW RobotsWireless connectivity and Cryptography are a big topicTechnical assistance for junior developersClose collaboration with internal stakeholders like sales, application managers etc.Your experience:Fluency in English is a MUSTEITHER a Bachelor's degree in software engineering or computer science, OR relevant technical industry experienceHands-on experience in an embedded software environment with C/C++ on LinuxSome touchpoints and experience in cryptographic topicsExperienced in OOD, OOP and Embedded ARM and RTOS are extremely beneficialExperience with scripting languages such as Bash, Python or elseKnowledge of Wireless communicationKnowledge of Development Tools such as Jenkins, Jira or Git are a huge plusIf you are interested in this opportunity and would like to get to know more about it, please do not hesitate to contact me and send in your application.At this point, we can only consider applications with a valid work permit for Switzerland.

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