191 jobs found in Luterbach, Solothurn - Page 1

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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 at least 4 years experience in QA? You should then read the following lines! Our client, based in Solothurn, is looking for a Quality Assurance Operations Associate III for a 8 months contract. The Quality Assurance 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 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.As such, the position is expected to have knowledge in cell culture, purifications process, operations and business processes within a GMP Biotech environment. Previous experience with manufacturing execution systems (Delta V/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.You work on the field, having an oversight over the manufacturing operations from a quality point of view and the electronic batch record review (QRM). You will review and approve Standard Operating Procedures (SOP) and you will perform ad hoc sampling and testing. You report to the Quality Assurance Operations Supervisor and work cross-functional with different quality units (QC, Product Quality, Corporate Quality, QA). You work in a 5-shift model along side the manufacturing team, within this you will work with other Quality Assurance Operations Associate colleagues and your Supervisor. QUALIFICATIONS:Previous experience in quality assurance and/or operation experience in pharmaceutical or biotech manufacturing environment. Prior experience with fully electronic operations and management is preferred.Good experience of process design and improvement.Strong working experience with GxP regulationsElectronic Batch Record and elogbook management will be an asset KNOWLEDGE AND SKILLS:Good oral and written communication skills and ability to communicate with all levels of management, peers, contractors and external partners effectivelyDemonstrated ability to work autonomously and lead projectCandidates with experience in drug substance (or API) and drug product are preferred.Demonstrated problem solving skillsProficiencies with the Quality systems and business processes associated with automation and integration of testing and production systems.Must have strong technical skills and be proficient with typical productivity software (Word, Excel, Powerpoint, Visio, etc.)Ability to work in shift model (night as well) including during the weekend Do not waste any minutes, apply now!  We are looking forward to receiving your application. 
    Do you want to work in a biotech company? Do you have at least 4 years experience in QA? You should then read the following lines! Our client, based in Solothurn, is looking for a Quality Assurance Operations Associate III for a 8 months contract. The Quality Assurance 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 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.As such, the position is expected to have knowledge in cell culture, purifications process, operations and business processes within a GMP Biotech environment. Previous experience with manufacturing execution systems (Delta V/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.You work on the field, having an oversight over the manufacturing operations from a quality point of view and the electronic batch record review (QRM). You will review and approve Standard Operating Procedures (SOP) and you will perform ad hoc sampling and testing. You report to the Quality Assurance Operations Supervisor and work cross-functional with different quality units (QC, Product Quality, Corporate Quality, QA). You work in a 5-shift model along side the manufacturing team, within this you will work with other Quality Assurance Operations Associate colleagues and your Supervisor. QUALIFICATIONS:Previous experience in quality assurance and/or operation experience in pharmaceutical or biotech manufacturing environment. Prior experience with fully electronic operations and management is preferred.Good experience of process design and improvement.Strong working experience with GxP regulationsElectronic Batch Record and elogbook management will be an asset KNOWLEDGE AND SKILLS:Good oral and written communication skills and ability to communicate with all levels of management, peers, contractors and external partners effectivelyDemonstrated ability to work autonomously and lead projectCandidates with experience in drug substance (or API) and drug product are preferred.Demonstrated problem solving skillsProficiencies with the Quality systems and business processes associated with automation and integration of testing and production systems.Must have strong technical skills and be proficient with typical productivity software (Word, Excel, Powerpoint, Visio, etc.)Ability to work in shift model (night as well) including during the weekend Do not waste any minutes, apply now!  We are looking forward to receiving your application. 
    • 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.
    • 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
    • contract
    Do you want to work in a biotech company? Do you have a first experience in a GMP environment? You should then read the following lines! Our client, based in Solothurn, is looking for a Manufacturing Associate for a 1 year-mission. JOB SUMMARY:Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation. Ensures compliance to cGMP as well as maintaining equipment and facilities. The manufacturing associate is detail-oriented with strong understanding of automated systems and process controls. Individual will maintain training to the required level and support other functions on site.Executes manufacturing processing steps and/or manufacturing support activities using electronic batch records RESPONSIBILITIES:- Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentation- Actively participates in training activities, managing their individual training plan. Trains other associates as required.- Executes validation protocols- And other job duties that may be assigned from time to time. REQUIREMENTS:• High school diploma or equivalent experience and typically 3-5 years relevant experience in related or non-related industry or 2-3 years experience in Pharma/Biotech industryOR• Bachelor degree in related filed with 1-2 years professional experienceOR• Bachelor degree in not related field and typically 3-4 years experience• Languages: English B1, German and/or French an assetShift work is required for this position Do not waste any minutes, apply now! We are looking forward to receiving your application.
    Do you want to work in a biotech company? Do you have a first experience in a GMP environment? You should then read the following lines! Our client, based in Solothurn, is looking for a Manufacturing Associate for a 1 year-mission. JOB SUMMARY:Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, and revising cGMP documentation. Ensures compliance to cGMP as well as maintaining equipment and facilities. The manufacturing associate is detail-oriented with strong understanding of automated systems and process controls. Individual will maintain training to the required level and support other functions on site.Executes manufacturing processing steps and/or manufacturing support activities using electronic batch records RESPONSIBILITIES:- Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentation- Actively participates in training activities, managing their individual training plan. Trains other associates as required.- Executes validation protocols- And other job duties that may be assigned from time to time. REQUIREMENTS:• High school diploma or equivalent experience and typically 3-5 years relevant experience in related or non-related industry or 2-3 years experience in Pharma/Biotech industryOR• Bachelor degree in related filed with 1-2 years professional experienceOR• Bachelor degree in not related field and typically 3-4 years experience• Languages: English B1, German and/or French an assetShift work is required for this position Do not waste any minutes, apply now! We are looking forward to receiving your application.
    • 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
    • temp to perm
    Für unseren Kunden im Raum Solothurn suchen zur Verstärkung des Logistikteams einen motivierten, selbständigen und flexiblenLogistiker EFZ / EBA (w/m)Zu Ihrem Verantwortungsbereich gehören folgende Aufgaben:Führung der AbladegruppeWareneingangskontrolleFrachtpapiere kontrollieren und unterschreibenAufnahme und Kontrolle der WareAufträge korrekt ausfüllen und bei Bedarf Muster entnehmenWegleitung der Ware sicherstellen und organisierenZeitnahe Entladung der LKWAllgemeine Lagerarbeiten und Lagerpflege
    Für unseren Kunden im Raum Solothurn suchen zur Verstärkung des Logistikteams einen motivierten, selbständigen und flexiblenLogistiker EFZ / EBA (w/m)Zu Ihrem Verantwortungsbereich gehören folgende Aufgaben:Führung der AbladegruppeWareneingangskontrolleFrachtpapiere kontrollieren und unterschreibenAufnahme und Kontrolle der WareAufträge korrekt ausfüllen und bei Bedarf Muster entnehmenWegleitung der Ware sicherstellen und organisierenZeitnahe Entladung der LKWAllgemeine Lagerarbeiten und Lagerpflege
    • derendingen, solothurn
    • permanent
    Unsere Mandantin ist ein KMU Betrieb mit der Spezialisierung beschichten und lackieren von Industrie-, Sanitär-, Transport- und Elektronik Produkten. Um das Team zu erweitern und damit die Produktion sicher zu stellen und die Aufträge wie geplant erfüllen zu können, suchen wir einen Lackierer oder Lackiererin mit Erfahrung mit verschiedenen Lacksystemen.Ihr Aufgabengebiet umfasst folgende Themen:Vorbereitungsarbeiten zur Lackierung wie abdecken, schleifen & spachtelnLackierarbeiten auf unterschiedlichen MaterialienEinrichten, programmieren und bedienen des Lackierroboters Durchführen, auswerten und rapportieren der Erstmusterprüfungen und Endkontrollen. Stetige ProzessoptimierungZusammenarbeit mit der AVOR im Bezug der Mengen, Termine und QualitätEinhaltung der Arbeitssicherheits- und Gesundheitsvorgaben
    Unsere Mandantin ist ein KMU Betrieb mit der Spezialisierung beschichten und lackieren von Industrie-, Sanitär-, Transport- und Elektronik Produkten. Um das Team zu erweitern und damit die Produktion sicher zu stellen und die Aufträge wie geplant erfüllen zu können, suchen wir einen Lackierer oder Lackiererin mit Erfahrung mit verschiedenen Lacksystemen.Ihr Aufgabengebiet umfasst folgende Themen:Vorbereitungsarbeiten zur Lackierung wie abdecken, schleifen & spachtelnLackierarbeiten auf unterschiedlichen MaterialienEinrichten, programmieren und bedienen des Lackierroboters Durchführen, auswerten und rapportieren der Erstmusterprüfungen und Endkontrollen. Stetige ProzessoptimierungZusammenarbeit mit der AVOR im Bezug der Mengen, Termine und QualitätEinhaltung der Arbeitssicherheits- und Gesundheitsvorgaben
    • zuchwil, solothurn
    • permanent
    Du bist ein gelernter Elektroinstallateur mit Weiterbildung zum SIBE und arbeitest gerne selbständig? Dann suchen wir dich für eine spannende Aufgabe im Raum Solothurn!Elektro-Sicherheitsberater(m/w) 80 - 100%Deine Aufgaben: Technische Betreuung des Meldewesens Strom von der Überprüfung derankommenden NIV/NIN Formulare bis zur Auslösung von StichprobenkontrollenEigenständiges Durchführen von Stichprobenkontrollen je nach RessourcenBearbeiten von Anschlussgesuchen für Geräte und Anlagen (Photovoltaikanlagen) in Zusammenarbeit mit dem Bereich Strom Erstellen von Kontrollberichten und SicherheitsnachweisenKontrolle der innerbetrieblichen InstallationenKompetende Beratung unserer Installateure und Kunden in NIV/NINThematiken
    Du bist ein gelernter Elektroinstallateur mit Weiterbildung zum SIBE und arbeitest gerne selbständig? Dann suchen wir dich für eine spannende Aufgabe im Raum Solothurn!Elektro-Sicherheitsberater(m/w) 80 - 100%Deine Aufgaben: Technische Betreuung des Meldewesens Strom von der Überprüfung derankommenden NIV/NIN Formulare bis zur Auslösung von StichprobenkontrollenEigenständiges Durchführen von Stichprobenkontrollen je nach RessourcenBearbeiten von Anschlussgesuchen für Geräte und Anlagen (Photovoltaikanlagen) in Zusammenarbeit mit dem Bereich Strom Erstellen von Kontrollberichten und SicherheitsnachweisenKontrolle der innerbetrieblichen InstallationenKompetende Beratung unserer Installateure und Kunden in NIV/NINThematiken
    • zuchwil, solothurn
    • temporary
    Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.Main ResponsibilitiesThe Supply Planning Analyst role is providing support for project driven supply planning and product variant introduction through the supply chain. Ensures a strong alignment with business partners and drives process improvements. Supports the Planning Professionals in the operational process of the Product Version phase-in, phase-out activities of medical device products.Coordinator for Variant introduction within Supply ChainMonitor implementation and owing the execution to ensure smooth transition of variant codes into Supply ChainPrepare inputs for Demand Planning, system set-up and cutover plan for Supply Network PlanningContribute to project teams through the variant implementation processLead process improvements of the end-to-end Variant process in collaboration with affected departmentsHandle the impact of license expiry on end-to-end supply chain planning activityProvide meaningful analytics and important metric reportingTrain users and partners on Variant processes and systemsKnow and follow all laws and policies to apply the job and maintain the highest level of integrity, ethics and compliance at all time
    Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.Main ResponsibilitiesThe Supply Planning Analyst role is providing support for project driven supply planning and product variant introduction through the supply chain. Ensures a strong alignment with business partners and drives process improvements. Supports the Planning Professionals in the operational process of the Product Version phase-in, phase-out activities of medical device products.Coordinator for Variant introduction within Supply ChainMonitor implementation and owing the execution to ensure smooth transition of variant codes into Supply ChainPrepare inputs for Demand Planning, system set-up and cutover plan for Supply Network PlanningContribute to project teams through the variant implementation processLead process improvements of the end-to-end Variant process in collaboration with affected departmentsHandle the impact of license expiry on end-to-end supply chain planning activityProvide meaningful analytics and important metric reportingTrain users and partners on Variant processes and systemsKnow and follow all laws and policies to apply the job and maintain the highest level of integrity, ethics and compliance at all time
    • zuchwil, solothurn
    • temporary
    Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.Main ResponsibilitiesAs part of the Regulatory Compliance team of DePuySynthes, this role provides Quality System Compliance support to the assigned site(s). This includes the procedures and records required for the development, deployment and maintenance of quality system processes in order to assure the ongoing compliance with ISO13485, FDA QSRs and the Medical Devices Directive and other applicable regulations and standards.Prepare and maintain regulatory inspection readiness plans for assigned sitesExecute internal audit as per approved schedule for other DePuy Synthes sites (worldwide scope, products and technologies)Lead all assigned quality actions, and ensure all internal and external audit observations are investigated, have causes identified, action plans completed, and appropriate effectiveness monitoringEnsure proper internal audit reporting, response review and approvals, communication of issues, and use of tracking and trending tools to monitor site compliance performanceCoach and develop users on Audit system as well as regulation requirementsDrive Compliance improvements, which result from internal audits, Quality Board Issues and other system indicatorsProvide Front Room/ Back Room support during external auditsGuide Quality System Auditors and support staff as required to ensure appropriate control systems are in place and continually improved to meet changing regulatory, corporate and industry standards
    Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.Main ResponsibilitiesAs part of the Regulatory Compliance team of DePuySynthes, this role provides Quality System Compliance support to the assigned site(s). This includes the procedures and records required for the development, deployment and maintenance of quality system processes in order to assure the ongoing compliance with ISO13485, FDA QSRs and the Medical Devices Directive and other applicable regulations and standards.Prepare and maintain regulatory inspection readiness plans for assigned sitesExecute internal audit as per approved schedule for other DePuy Synthes sites (worldwide scope, products and technologies)Lead all assigned quality actions, and ensure all internal and external audit observations are investigated, have causes identified, action plans completed, and appropriate effectiveness monitoringEnsure proper internal audit reporting, response review and approvals, communication of issues, and use of tracking and trending tools to monitor site compliance performanceCoach and develop users on Audit system as well as regulation requirementsDrive Compliance improvements, which result from internal audits, Quality Board Issues and other system indicatorsProvide Front Room/ Back Room support during external auditsGuide Quality System Auditors and support staff as required to ensure appropriate control systems are in place and continually improved to meet changing regulatory, corporate and industry standards
    • zuchwil, solothurn
    • permanent
    Sind Sie ein motivierter Montage-Elektriker im Raum Solothurn, der seine Fähigkeiten unter Beweis stellen will. Unser Kunde in Zuchwil sucht ab sofort oder nach Vereinbarung einen: Montage-Elektriker (m/w) 100%Ihre Aufgaben:Installationen im Bereich Stark- und SchwachstromNeu- sowie UmbauarbeitenOrganisieren des Arbeitsplatzes Unterstützung bei der Materialwirtschaft
    Sind Sie ein motivierter Montage-Elektriker im Raum Solothurn, der seine Fähigkeiten unter Beweis stellen will. Unser Kunde in Zuchwil sucht ab sofort oder nach Vereinbarung einen: Montage-Elektriker (m/w) 100%Ihre Aufgaben:Installationen im Bereich Stark- und SchwachstromNeu- sowie UmbauarbeitenOrganisieren des Arbeitsplatzes Unterstützung bei der Materialwirtschaft
    • zuchwil, solothurn
    • temporary
    Hast du eine Grundausbildung in der Automobilbranche und suchst eine passende Stelle in diesem Bereich? Dann suchen wir dich als: Reifenpraktiker Ihr Aufgabenbereich:• Reifenservice an verschiedenen Personenwagen, Nutzfahrzeugen• Wartungs- und Servicearbeiten an PW, NFZ nach Ausbildungsstand• Aktive Mitarbeit im Werkstatt-Team• Einlagerung von Räder/Reifen• Instandhaltung und Pflege der Arbeitsgeräte
    Hast du eine Grundausbildung in der Automobilbranche und suchst eine passende Stelle in diesem Bereich? Dann suchen wir dich als: Reifenpraktiker Ihr Aufgabenbereich:• Reifenservice an verschiedenen Personenwagen, Nutzfahrzeugen• Wartungs- und Servicearbeiten an PW, NFZ nach Ausbildungsstand• Aktive Mitarbeit im Werkstatt-Team• Einlagerung von Räder/Reifen• Instandhaltung und Pflege der Arbeitsgeräte
    • zuchwil, solothurn
    • temporary
    Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.Main Responsibilities:The Document Management Change Analyst is accountable for the administration of the Change Order (CO) process. This includes the timely processing and release of new and changed controlled documents.Controlling and release of change requests Release of change ordersSupport the end users in creation of changesSupport the end users in handling of the office application (Word, Excel)
    Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.DePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings, help advance the health and wellbeing of people around the world.Main Responsibilities:The Document Management Change Analyst is accountable for the administration of the Change Order (CO) process. This includes the timely processing and release of new and changed controlled documents.Controlling and release of change requests Release of change ordersSupport the end users in creation of changesSupport the end users in handling of the office application (Word, Excel)
    • zuchwil, solothurn
    • temporary
    Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und eint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.DePuy Synthes Companies of Johnson & Johnson ist das größte und umfassendste Orthopädieunternehmen der Welt. DePuy Synthes bietet eine beispiellose Breite und Tiefe unterschiedlicher Technologien, Produkte, Dienstleistungen und Programme in den Bereichen Orthopädie, Traumatologie, Wirbelsäule, Sportmedizin, Neurologie, Gesichts- und Schädelchirurgie, Power Tools und Biomaterialien an. Unsere breite Palette an innovativen und qualitativ hochwertigen Angeboten trägt dazu bei, die Gesundheit und das Wohlbefinden von Menschen auf der ganzen Welt nachhaltig zu verbessern. Zu den Haupttätigkeiten gehören unter anderem:Prüfung und Freigabe von Änderungsan- und aufträgen unter Einhaltung der geltenden Richtlinien und VerfahrenUnterstützung der Endanwender bei der Erstellung von Änderungen und im Umgang mit der Office-Anwendung (Word, Excel)Verantwortlich für die Einhaltung der regulatorischen und Compliance-Anforderungen in Bezug auf Dokumentation und DokumentationsmanagementTermingerechte Bearbeitung und Freigabe neuer und geänderten Richtlinien/Prozessen/ArbeitsanweisungenMonatliche Datenauswertungen Unterstützung und Mitarbeit an diversen Business Projekten
    Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und eint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.DePuy Synthes Companies of Johnson & Johnson ist das größte und umfassendste Orthopädieunternehmen der Welt. DePuy Synthes bietet eine beispiellose Breite und Tiefe unterschiedlicher Technologien, Produkte, Dienstleistungen und Programme in den Bereichen Orthopädie, Traumatologie, Wirbelsäule, Sportmedizin, Neurologie, Gesichts- und Schädelchirurgie, Power Tools und Biomaterialien an. Unsere breite Palette an innovativen und qualitativ hochwertigen Angeboten trägt dazu bei, die Gesundheit und das Wohlbefinden von Menschen auf der ganzen Welt nachhaltig zu verbessern. Zu den Haupttätigkeiten gehören unter anderem:Prüfung und Freigabe von Änderungsan- und aufträgen unter Einhaltung der geltenden Richtlinien und VerfahrenUnterstützung der Endanwender bei der Erstellung von Änderungen und im Umgang mit der Office-Anwendung (Word, Excel)Verantwortlich für die Einhaltung der regulatorischen und Compliance-Anforderungen in Bezug auf Dokumentation und DokumentationsmanagementTermingerechte Bearbeitung und Freigabe neuer und geänderten Richtlinien/Prozessen/ArbeitsanweisungenMonatliche Datenauswertungen Unterstützung und Mitarbeit an diversen Business Projekten
    • solothurn, solothurn
    • permanent
    Unser Kunde bietet dir einen modernen Arbeitsplatz mit abwechslungsreichen Aufgaben und guten Anstellungsbedingungen als: Sachbearbeiter Innendienst 80% (m/w/d) Deine Tätigkeiten: Du empfängst die Kunden und Geschäftspartner und stellst damit die erste Anlaufstelle dar Mit deinen guten Sprachkenntnissen (DE/FR) beantwortest du die telefonischen und schriftlichen Anfragen und Reklamationen der KundenDie Kunden berätst du kompetent zu den bestehenden Dienstleistungen Ebenfalls liegt die optimale Disposition der Dienstleistungsaufträge und des Servicepersonal in deiner Aufgabe Mit deiner exakte Arbeitsweise hälst du die Kundenstammdaten im Betriebssystem immer auf dem laufenden Stand
    Unser Kunde bietet dir einen modernen Arbeitsplatz mit abwechslungsreichen Aufgaben und guten Anstellungsbedingungen als: Sachbearbeiter Innendienst 80% (m/w/d) Deine Tätigkeiten: Du empfängst die Kunden und Geschäftspartner und stellst damit die erste Anlaufstelle dar Mit deinen guten Sprachkenntnissen (DE/FR) beantwortest du die telefonischen und schriftlichen Anfragen und Reklamationen der KundenDie Kunden berätst du kompetent zu den bestehenden Dienstleistungen Ebenfalls liegt die optimale Disposition der Dienstleistungsaufträge und des Servicepersonal in deiner Aufgabe Mit deiner exakte Arbeitsweise hälst du die Kundenstammdaten im Betriebssystem immer auf dem laufenden Stand
    • solothurn, solothurn
    • temporary
    Sie kennen sich mit Apps aus und können mit einem PC umgehen? Wir suchen Dich als Tester für ein neues App für die Medizinbranche. Helfen Sie mit ein neues Innovatives und hilfreiches App mit zu entwickeln. Aufgabe:Tool basiertes testen einer mobile App über PC'sDokumentieren der Ergebnisse Toll Basiert Sicherstellen des TestplanesSelbstständiges Testen anhand eines PlanesSupport
    Sie kennen sich mit Apps aus und können mit einem PC umgehen? Wir suchen Dich als Tester für ein neues App für die Medizinbranche. Helfen Sie mit ein neues Innovatives und hilfreiches App mit zu entwickeln. Aufgabe:Tool basiertes testen einer mobile App über PC'sDokumentieren der Ergebnisse Toll Basiert Sicherstellen des TestplanesSelbstständiges Testen anhand eines PlanesSupport
    • solothurn, solothurn
    • temporary
    Für die Welt sorgen ...beim Einzelnen beginnen. Dieser Leitsatz inspiriert und eint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.Die Johnson & Johnson AG ist führend im Vertrieb von medizinischen Geräten.Deine Haupttätigkeiten:In dieser Funktion gehörst du zum First Point of Contact und stellst einen exzellenten Service für externe als auch interne Kunden sicher. Du verstehst den Kunden als Partner und arbeitest an der Vision Customer Service Excellence.Selbständige Erfassung aller Kundenbestellungen am selben Tag in hoher ServicequalitätAbwicklung von Bestellaufträgen in DeutschEntgegennehmen von Bestellungen der Spitäler, Ärzte und AussendienstmitarbeiterVerbrauchsmeldungen entgegennehmen, bearbeiten und verrechnenFakturierung und Erstellung von GutschriftenEnge Zusammenarbeit mit internen Stellen (Lager, Pricing, Verkauf, Product Manager)Allgemeine administrative Tätigkeiten
    Für die Welt sorgen ...beim Einzelnen beginnen. Dieser Leitsatz inspiriert und eint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.Die Johnson & Johnson AG ist führend im Vertrieb von medizinischen Geräten.Deine Haupttätigkeiten:In dieser Funktion gehörst du zum First Point of Contact und stellst einen exzellenten Service für externe als auch interne Kunden sicher. Du verstehst den Kunden als Partner und arbeitest an der Vision Customer Service Excellence.Selbständige Erfassung aller Kundenbestellungen am selben Tag in hoher ServicequalitätAbwicklung von Bestellaufträgen in DeutschEntgegennehmen von Bestellungen der Spitäler, Ärzte und AussendienstmitarbeiterVerbrauchsmeldungen entgegennehmen, bearbeiten und verrechnenFakturierung und Erstellung von GutschriftenEnge Zusammenarbeit mit internen Stellen (Lager, Pricing, Verkauf, Product Manager)Allgemeine administrative Tätigkeiten
    • 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.
    • solothurn, solothurn
    • temporary
    Willst du bei der Umrüstung auf erneuerbare Energien mitwirken und bist zu dem ein Organisationstalent? Dann suchen wir Dich zur Verstärkung des Teams als:Allrounder / Monteur Bau 100%Ihre Aufgaben: Montage von Photovoltaik-Anlagen auf Steil- und Flachdächern Direkte Zusammenarbeit mit dem ProjektleiterDiverse Hilfsarbeiten auf dem Dach
    Willst du bei der Umrüstung auf erneuerbare Energien mitwirken und bist zu dem ein Organisationstalent? Dann suchen wir Dich zur Verstärkung des Teams als:Allrounder / Monteur Bau 100%Ihre Aufgaben: Montage von Photovoltaik-Anlagen auf Steil- und Flachdächern Direkte Zusammenarbeit mit dem ProjektleiterDiverse Hilfsarbeiten auf dem Dach
    • solothurn, solothurn
    • temporary
    Du kennst Dich mit Apps aus und kannst mit einem PC umgehen? Wir suchen Dich als Tester für ein neues App für die Medizinbranche. Helfe mit ein neues Innovatives und hilfreiches App mit zu entwickeln. Tool basiertes testen einer mobile App über PC'sDokumentieren der Ergebnisse Toll Basiert Sicherstellen des TestplanesSelbstständiges Testen anhand eines PlanesSupport
    Du kennst Dich mit Apps aus und kannst mit einem PC umgehen? Wir suchen Dich als Tester für ein neues App für die Medizinbranche. Helfe mit ein neues Innovatives und hilfreiches App mit zu entwickeln. Tool basiertes testen einer mobile App über PC'sDokumentieren der Ergebnisse Toll Basiert Sicherstellen des TestplanesSelbstständiges Testen anhand eines PlanesSupport
    • solothurn, solothurn
    • temporary
    Wir suchen Sie als Mitarbeiter oder Mitarbeiterin bei unserem Kunden für die Abteilung Spritzerei Unser Kunde ist ein weltweit führendes Unternehmen im der Medizin Branche. Bedienen der Montage- und DruckanlagenBedienen der Verpackungsanlagen gemäss Vorschriften Einhalten der geforderten Qualität und QuantitätSelbstständige Behebung allfälliger Störungen an den AnlagenPrüf- und Reinigungsarbeiten gemäss RichtlinienMitarbeit in der Inspektion und Wartung an den AnlagenArbeiten 4-Schichtbetrieb ist zwingendProzesse und Richtlinien strikt einhalten Erkennen und Melden von AbweichungenFlexibel einsetzbar in der Montage und im Bereich Spritzguss
    Wir suchen Sie als Mitarbeiter oder Mitarbeiterin bei unserem Kunden für die Abteilung Spritzerei Unser Kunde ist ein weltweit führendes Unternehmen im der Medizin Branche. Bedienen der Montage- und DruckanlagenBedienen der Verpackungsanlagen gemäss Vorschriften Einhalten der geforderten Qualität und QuantitätSelbstständige Behebung allfälliger Störungen an den AnlagenPrüf- und Reinigungsarbeiten gemäss RichtlinienMitarbeit in der Inspektion und Wartung an den AnlagenArbeiten 4-Schichtbetrieb ist zwingendProzesse und Richtlinien strikt einhalten Erkennen und Melden von AbweichungenFlexibel einsetzbar in der Montage und im Bereich Spritzguss
    • solothurn, solothurn
    • temporary
    Sind Sie sich gewohnt in einer kleinen und familiären Praxis zu Arbeiten und Ihr bestes zu geben? Dann habe ich evtl. was für Sie:Med. Praxisassistentin 20-30%Bedienung der TelefonzentraleRöntgenVollelektronische Führung der PatientenakteSchreiben von Berichten ab DiktaphonAssistieren Ausführen von BestellungenLabor
    Sind Sie sich gewohnt in einer kleinen und familiären Praxis zu Arbeiten und Ihr bestes zu geben? Dann habe ich evtl. was für Sie:Med. Praxisassistentin 20-30%Bedienung der TelefonzentraleRöntgenVollelektronische Führung der PatientenakteSchreiben von Berichten ab DiktaphonAssistieren Ausführen von BestellungenLabor
    • solothurn, solothurn
    • temporary
    Haben Sie Kenntnisse im Fachgebiet der Orthopädie und suchen eine temporäre Stelle bis ende Jahr in einem Modernen Umfeld? Wir suchen: Med. Praxisassistentin 50-100%Bedienung der TelefonzentraleSprechstundenvorbereitung Vollelektronische Führung der PatientenakteSchreiben von Berichten ab DiktaphonBedienung des EmpfangsTerminvereinbarung
    Haben Sie Kenntnisse im Fachgebiet der Orthopädie und suchen eine temporäre Stelle bis ende Jahr in einem Modernen Umfeld? Wir suchen: Med. Praxisassistentin 50-100%Bedienung der TelefonzentraleSprechstundenvorbereitung Vollelektronische Führung der PatientenakteSchreiben von Berichten ab DiktaphonBedienung des EmpfangsTerminvereinbarung
    • solothurn, solothurn
    • contract
    Do you want to work in a big medical devices company? Do you have experience in Project Management for Medical Devices? You should then read the following lines! Our client, based in the Solothurn area, is looking for a Project Manager - Regulatory Affairs for a one year contract. Job Description:Support MDR compliance execution work by acting as project manager who has oversight on ongoing MDR compliance work for Trauma/CMF/BIO and drives completion of MDR deliverables. This activity includes but is not limited to:- Coordinate and drive resolving of NB questions to submitted Technical Documentation- Provide regular status updates on MDR compliance progress for Trauma/CMF/BIO to MDR PMO and governance team.- Facilitate resolving of roadblocks and timeline constraints- Support execution of project plan for MDR compliance in Trauma/CMF/BIO business for 2021/ 2022.- Lead regular status update meetings with corresponding teams who are working on individual MDR files and/ or specific topics- Lead and track cross-functional activities as assigned, such as MDR Indication definition and Technical Documentation submissions to Notified Body- Provide project management support for activities needed in preparation for MDR compliance as instructed and assigned. What we need from the candidate:• At least 2 years Project Management experience within Medical Device industry• Basic understanding of MDR requirements regarding required content of Technical Documentation (focus on ANNEX II of Regulation (EU) 2017/745).• Excellent person interaction skills and reliable and goal oriented work attitude• Experienced skills in MS Office, especially in MS Project• Strong analytical skills• Fluent in English. German in addition, would be an asset. 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 big medical devices company? Do you have experience in Project Management for Medical Devices? You should then read the following lines! Our client, based in the Solothurn area, is looking for a Project Manager - Regulatory Affairs for a one year contract. Job Description:Support MDR compliance execution work by acting as project manager who has oversight on ongoing MDR compliance work for Trauma/CMF/BIO and drives completion of MDR deliverables. This activity includes but is not limited to:- Coordinate and drive resolving of NB questions to submitted Technical Documentation- Provide regular status updates on MDR compliance progress for Trauma/CMF/BIO to MDR PMO and governance team.- Facilitate resolving of roadblocks and timeline constraints- Support execution of project plan for MDR compliance in Trauma/CMF/BIO business for 2021/ 2022.- Lead regular status update meetings with corresponding teams who are working on individual MDR files and/ or specific topics- Lead and track cross-functional activities as assigned, such as MDR Indication definition and Technical Documentation submissions to Notified Body- Provide project management support for activities needed in preparation for MDR compliance as instructed and assigned. What we need from the candidate:• At least 2 years Project Management experience within Medical Device industry• Basic understanding of MDR requirements regarding required content of Technical Documentation (focus on ANNEX II of Regulation (EU) 2017/745).• Excellent person interaction skills and reliable and goal oriented work attitude• Experienced skills in MS Office, especially in MS Project• Strong analytical skills• Fluent in English. German in addition, would be an asset. 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. 
    • zug, zug
    • temporary
    Do you have a first experience with complaint handling ? Do you want to participate in the development of a new complaint handling strategy in a multinational environment ? You should then read the following lines!One of our clients, a renowned life science company based in the Zug area, is looking for a new member for their Technical Production Complaint team. They offer a mission of 9 months at first, with the possibility of extension. Tasks:Assess current post market activities to understand scope of how feedback is received, captured, trended and fed back into various teams and assess gaps against various Medical Device and combination product requirements utilizing current gap analysis and by interviewing customer interfacing teamsCollaborate with quality and regulatory to align on the approach to take going forward, regarding feedback gatheringWork with customer interfacing teams to establish processes required and ensure implementation in the QMS for the applicable Medical Device product (Konektom, MSPT, titration device (Peg IM, Avonex)) in line with the expectations of ISO13485 and EU Medical Device RegulationWork with TPC team to ensure correct implementation of feedback loop from Use error and feedback to allow correct classification, trending and input into usability, performance and safety requirements Work with TD/ PPD to ensure correct implementation of updated design control and risk management procedures through translating TPC feedback data to design/ risk management documents for medical devices and combination devices The mentioned tasks sound appealing to you ? Do not waste a second then, and apply now!
    Do you have a first experience with complaint handling ? Do you want to participate in the development of a new complaint handling strategy in a multinational environment ? You should then read the following lines!One of our clients, a renowned life science company based in the Zug area, is looking for a new member for their Technical Production Complaint team. They offer a mission of 9 months at first, with the possibility of extension. Tasks:Assess current post market activities to understand scope of how feedback is received, captured, trended and fed back into various teams and assess gaps against various Medical Device and combination product requirements utilizing current gap analysis and by interviewing customer interfacing teamsCollaborate with quality and regulatory to align on the approach to take going forward, regarding feedback gatheringWork with customer interfacing teams to establish processes required and ensure implementation in the QMS for the applicable Medical Device product (Konektom, MSPT, titration device (Peg IM, Avonex)) in line with the expectations of ISO13485 and EU Medical Device RegulationWork with TPC team to ensure correct implementation of feedback loop from Use error and feedback to allow correct classification, trending and input into usability, performance and safety requirements Work with TD/ PPD to ensure correct implementation of updated design control and risk management procedures through translating TPC feedback data to design/ risk management documents for medical devices and combination devices The mentioned tasks sound appealing to you ? Do not waste a second then, and apply now!
    • solothurn, solothurn
    • permanent
    Im Auftrag unserer Kunden, ein namhaftes Unternehmen aus der Region, suchen wir ab sofort einen Polymechaniker mit Erfahrung im Bereich CNC Kurzdrehen.Hauptaufgaben: Einrichten und Betreuen von CNC-Kurzdrehmaschinen Typ NakamuraDurchführen von Erststück-, Zwischen- und Endprüfungen Durchführen von SPC-Messungen Wechseln der Werkzeuge und vornehmen von Korrekturen Programmieren von neuen Werkstücken
    Im Auftrag unserer Kunden, ein namhaftes Unternehmen aus der Region, suchen wir ab sofort einen Polymechaniker mit Erfahrung im Bereich CNC Kurzdrehen.Hauptaufgaben: Einrichten und Betreuen von CNC-Kurzdrehmaschinen Typ NakamuraDurchführen von Erststück-, Zwischen- und Endprüfungen Durchführen von SPC-Messungen Wechseln der Werkzeuge und vornehmen von Korrekturen Programmieren von neuen Werkstücken
    • solothurn, solothurn
    • temporary
    Du kennst Dich mit Apps aus und kannst mit einem PC umgehen? Wir suchen Dich als Tester für ein neues App für die Medizinbranche. Helfe mit ein neues Innovatives und hilfreiches App mit zu entwickeln. Tool basiertes testen einer mobile App über PC'sDokumentieren der Ergebnisse Toll Basiert Sicherstellen des TestplanesSelbstständiges Testen anhand eines PlanesSupport
    Du kennst Dich mit Apps aus und kannst mit einem PC umgehen? Wir suchen Dich als Tester für ein neues App für die Medizinbranche. Helfe mit ein neues Innovatives und hilfreiches App mit zu entwickeln. Tool basiertes testen einer mobile App über PC'sDokumentieren der Ergebnisse Toll Basiert Sicherstellen des TestplanesSelbstständiges Testen anhand eines PlanesSupport
    • solothurn, solothurn
    • temporary
    Wir suchen Sie als Mitarbeiter oder Mitarbeiterin bei unserem Kunden für die Abteilung Spritzerei Unser Kunde ist ein weltweit führendes Unternehmen im der Medizin Branche. Bedienen der Montage- und DruckanlagenBedienen der Verpackungsanlagen gemäss Vorschriften Einhalten der geforderten Qualität und QuantitätSelbstständige Behebung allfälliger Störungen an den AnlagenPrüf- und Reinigungsarbeiten gemäss RichtlinienMitarbeit in der Inspektion und Wartung an den AnlagenArbeiten 4-Schichtbetrieb ist zwingendProzesse und Richtlinien strikt einhalten Erkennen und Melden von AbweichungenFlexibel einsetzbar in der Montage und im Bereich Spritzguss
    Wir suchen Sie als Mitarbeiter oder Mitarbeiterin bei unserem Kunden für die Abteilung Spritzerei Unser Kunde ist ein weltweit führendes Unternehmen im der Medizin Branche. Bedienen der Montage- und DruckanlagenBedienen der Verpackungsanlagen gemäss Vorschriften Einhalten der geforderten Qualität und QuantitätSelbstständige Behebung allfälliger Störungen an den AnlagenPrüf- und Reinigungsarbeiten gemäss RichtlinienMitarbeit in der Inspektion und Wartung an den AnlagenArbeiten 4-Schichtbetrieb ist zwingendProzesse und Richtlinien strikt einhalten Erkennen und Melden von AbweichungenFlexibel einsetzbar in der Montage und im Bereich Spritzguss
    • solothurn, solothurn
    • temporary
    Wir suchen Sie als Mitarbeiter oder Mitarbeiterin bei unserem Kunden für die Abteilung Spritzerei Unser Kunde ist ein weltweit führendes Unternehmen im der Medizin Branche. Bedienen der Montage- und DruckanlagenBedienen der Verpackungsanlagen gemäss Vorschriften Einhalten der geforderten Qualität und QuantitätSelbstständige Behebung allfälliger Störungen an den AnlagenPrüf- und Reinigungsarbeiten gemäss RichtlinienMitarbeit in der Inspektion und Wartung an den AnlagenArbeiten 4-Schichtbetrieb ist zwingendProzesse und Richtlinien strikt einhalten Erkennen und Melden von AbweichungenFlexibel einsetzbar in der Montage und im Bereich Spritzguss
    Wir suchen Sie als Mitarbeiter oder Mitarbeiterin bei unserem Kunden für die Abteilung Spritzerei Unser Kunde ist ein weltweit führendes Unternehmen im der Medizin Branche. Bedienen der Montage- und DruckanlagenBedienen der Verpackungsanlagen gemäss Vorschriften Einhalten der geforderten Qualität und QuantitätSelbstständige Behebung allfälliger Störungen an den AnlagenPrüf- und Reinigungsarbeiten gemäss RichtlinienMitarbeit in der Inspektion und Wartung an den AnlagenArbeiten 4-Schichtbetrieb ist zwingendProzesse und Richtlinien strikt einhalten Erkennen und Melden von AbweichungenFlexibel einsetzbar in der Montage und im Bereich Spritzguss
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