Aktuelle Jobs im Zusammenhang mit Quality Assurance Specialist - Solothurn, Solothurn - Michael Page
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Quality Assurance Specialist
vor 1 Woche
Solothurn, Solothurn, Schweiz kollabo AG VollzeitJob Description: As a Quality Assurance Specialist at {company}, you will be responsible for ensuring the quality and integrity of our software products. Your mission will be to identify and report defects, develop and implement testing strategies, and work closely with cross-functional teams to deliver high-quality solutions. Key Responsibilities:•...
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IT Quality Assurance Manager
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IT Quality Assurance Manager
vor 3 Wochen
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IT Quality Assurance Manager
vor 3 Wochen
Solothurn, Solothurn, Schweiz Ypsomed VollzeitJobbeschreibung:Wir suchen eine technisch interessierte und engagierte Persönlichkeit als IT Quality Assurance Manager & CSV80. Ihre Hauptaufgaben sind die personelle und fachliche Führung der direkt unterstellten Mitarbeitenden im Team, die Beratung und Unterstützung von Systemeignern, Projektleitenden oder Lieferanten bei der Validierung von...
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Senior Clinical Research Specialist
Vor 3 Tagen
Solothurn, Solothurn, Schweiz Ypsomed VollzeitAbout the RoleWe are seeking a highly skilled and experienced Senior Clinical Research Specialist to join our team at Ypsomed.As a Senior Clinical Research Specialist, you will be responsible for overseeing global clinical trials, ensuring compliance with ISO standards, the Declaration of Helsinki, and relevant national laws and regulations.Responsible for...
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Décolletage Specialist
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Warehouse Operations Specialist
vor 13 Stunden
Solothurn, Solothurn, Schweiz Michael Page VollzeitThe Michael Page team is seeking a skilled Warehouse Operations Specialist to join our dynamic team.About the Role:This exciting opportunity involves overseeing all aspects of warehouse operations, ensuring seamless inventory management, shipping, and handling of Goods Manufacturing Practices (GMP) items. The ideal candidate will possess strong knowledge of...
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Human Factors Specialist
vor 1 Monat
Solothurn, Solothurn, Schweiz Ypsomed VollzeitAbout the RoleWe are seeking a highly skilled Human Factors Specialist to join our team at Ypsomed. As a key member of our Human Factors Engineering team, you will be responsible for planning and executing Human Factors Engineering programs according to current standards and guidelines.Key ResponsibilitiesDevelop and implement Human Factors Engineering...
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Clinical Research Specialist
vor 3 Wochen
Solothurn, Solothurn, Schweiz Ypsomed VollzeitAbout the RoleWe are seeking a highly skilled Clinical Research Specialist to join our team at Ypsomed. As a key member of our clinical research team, you will be responsible for overseeing global clinical trials, ensuring compliance with regulatory requirements, and collaborating with medical experts and external advisors.Key ResponsibilitiesOversee global...
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IT-Qualitätsmanager
vor 2 Wochen
Solothurn, Solothurn, Schweiz Ypsomed VollzeitPosition: IT-QualitätsmanagerWir suchen einen technisch interessierten und engagierte Manager IT-Qualität und Validierung, der sich in dem Bereich IT-Qualitätssicherung und Computer-System-Validierung auskennt. Als Teil des IT-Teams von Ypsomed AG sind Sie für die Personelle und fachliche Führung der direkt unterstellten Mitarbeitenden verantwortlich...
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Patrouilleur/in – Solothurn
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Solothurn, Solothurn, Schweiz TCS VollzeitCar Assistance SpecialistAs a Car Assistance Specialist at TCS, you will be responsible for ensuring the smooth operation of our vehicle fleet. Your tasks will include:Performing routine maintenance and repairs on vehiclesConducting quality control checks to ensure vehicles meet our high standardsCollaborating with our team to resolve any issues that may...
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Intensive Care Specialist
vor 3 Wochen
Solothurn, Solothurn, Schweiz Solothurner Spitäler AG VollzeitbJobResponsibilities/bulliDeliverhigh-quality,complexcaretopatientsontheintensivecareunit,includingmedical-technicalmonitoringandintensivemedicaltherapy./liliIndependentlyperformnursingandmedicalinterventionsforpatientswithcardiac,medical,andsurgicalconditions./liliCollaboratewithhealthcareprofessionalstoensureseamlesscarecoordination./liliCompletetheAdvance...
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Regulatory Affairs Specialist
vor 2 Monaten
Solothurn, Solothurn, Schweiz Ypsomed VollzeitAbout the RoleWe are seeking a highly skilled Regulatory Affairs Manager to join our team at Ypsomed. As a key member of our regulatory team, you will play a critical role in supporting our rapidly developing Diabetes Care business.Main ResponsibilitiesDevelop and implement regulatory strategies to ensure compliance with EU and US regulations.Prepare and...
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Solothurn, Solothurn, Schweiz Ypsomed VollzeitBerufliche Herausforderung:Wir suchen eine Persönlichkeit, die sich in der IT-Qualitätssicherung und Computer Systems Validation auskennt. Ihre Hauptaufgaben sind die fachliche und personelle Führung im Team, die Validierung von Computersystemen und die Erstellung von Dokumentationen.Wichtige Kenntnisse:Fundierte Kenntnisse in der IT-Sicherheit und...
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Child and Adolescent Psychiatry Specialist
vor 3 Wochen
Solothurn, Solothurn, Schweiz Solothurner Spitäler AG VollzeitbAmbulatoryChildandAdolescentPsychiatryServices/bbrbrOurChildandAdolescentPsychiatryDepartmentofferscomprehensivepsychiatriccareforchildren,adolescents,andtheirfamilies.Ourteamofspecialistsprovidesindividualizedtreatmentplans,tailoredtotheuniqueneedsofeachpatient.Weofferarangeofservices,includingambulatorytherapy,crisisintervention,andforensicpsychiatriceval...
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Regulatory Affairs Specialist
vor 2 Monaten
Solothurn, Solothurn, Schweiz Ypsomed Vollzeit{"Main Tasks* Develop and implement regulatory strategies to support the growth of our Diabetes Care business* Prepare and submit product documentation to regulatory authorities in the EU and US* Collaborate with business stakeholders to ensure regulatory compliance* Communicate with authorities and respond to regulatory inquiries* Participate in QMS ISO and...
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Regulatory Affairs Specialist
vor 1 Monat
Solothurn, Solothurn, Schweiz Ypsomed VollzeitJob Title: Regulatory Affairs ManagerAbout the Role:We are seeking a highly skilled Regulatory Affairs Manager to join our team at Ypsomed. As a key member of our regulatory team, you will be responsible for managing the development and implementation of regulatory strategies for our medical devices.Key Responsibilities:Develop and implement regulatory...
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Solothurn, Solothurn, Schweiz dynasoft AG VollzeitUnser AngebotBist Du bereit für eine Herausforderung im E-Commerce?Wir suchen einen erfahrenen Webshop-Entwickler, der leistungsstarke, individuelle Lösungen für unsere Kunden entwickelt.Entwicklung von Webshops im Bereich customized ERP-LösungenBetreuung von B2B-Shops und PlattformenQualitätsprüfung von Webshops und Implementierung neuer...
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Manufacturing Operations Specialist
vor 3 Wochen
Solothurn, Solothurn, Schweiz Michael Page VollzeitThe Senior Manufacturing Associate will be responsible for executing manufacturing processing steps and/or manufacturing support activities, monitoring upstream and downstream processes, and investigating and troubleshooting equipment/system setup issues. They will also validate protocols, revise cGMP documentation, and operate and maintain production...
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Regulatory Affairs Specialist
vor 2 Wochen
Solothurn, Solothurn, Schweiz Ypsomed VollzeitMain ResponsibilitiesSupport the development of Diabetes Care products, focusing on active and connected devices.Develop and implement regulatory strategies to ensure compliance with EU and US regulations.Prepare and submit product documentation to regulatory authorities.Collaborate with business stakeholders to achieve regulatory goals.Communicate with...
Quality Assurance Specialist
vor 2 Monaten
We are seeking a highly skilled Quality Control Engineer to join our team at Michael Page. As a key member of our Global QC Instrument and Equipment Strategy team, you will play a critical role in ensuring the quality and compliance of our analytical equipment and systems.
Key Responsibilities:- Harmonization and Lifecycle Management: Oversee the harmonization and lifecycle management of QC and MFG analytical equipment and systems across multiple sites.
- Project Management: Manage project activities including qualification, validation, decommissioning, and integration with computer systems.
- System Administration: Support system administration during validation and serve as backup administrator after system release for production.
- Compliance: Ensure compliance with internal policies and procedures across all stakeholders.
- Documentation and Scheduling: Prepare and review technical documents, manage workload scheduling, and ensure project prioritization, regulatory compliance, and collaboration with key teams (Quality, IT, validation, metrology, vendors).
- Procedure Development: Write and coordinate review of operational, maintenance, and system administration procedures for QC and MFG equipment.
- Education: Successfully completed academic degree.
- Experience: Minimum 2-4 years of working experience within a similar role in the pharmaceutical or biotechnological industry.
- Skills: Experience with managing analytical equipment and instruments in GMP Quality Control laboratories, familiarity with lab applications such as LabWare LIMS, Empower CDS, and vendor-supplied instrument control and data analysis software commonly used in QC laboratories in the pharmaceutical industry.
- Language Skills: Solid English skills, as well as very good German skills (verbally & written).
- Collaboration: Ability to develop effective working relationships with internal/external sites and cross-functional project teams.
