2 jobs found in Luterbach, Solothurn - Page 1

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    • 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.
    • 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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