With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
About us Your Contribution Possess knowledge and capabilities to execute Maintenance/Facilities Technician (all levels) roles and responsibilitiesMonitor daily work orders and employee activitiesCoordinate with various department stakeholders on Maintenance actionsHelp minimize machine downtimeLead, coach and train Maintenance TechniciansProcure parts, materials and resources to increase machine uptime; impart expertise and techniques to others within the departmentEstablish shift schedules to meet business needs; manage employee schedulesActively lead and participate in projects/events to drive improvementsFill in for the Maintenance Manager, as neededHelp with achieving department deliverables and initiatives Participate in the interviewing/hiring processHost meetings accordinglyEnsure clean and safe workspacesMaintain attendance within the payroll systemFollow cGMP and adhere to all ISO and safety guidelines and policies Your Profile High School Diploma or GED, required / Vocational school degree, preferredMinimum (3) years of maintenance/facilities experience in leading and directing the work of others in a fast-paced manufacturing settingStrong mechanical aptitudeUnderstanding of ISO and cGMPAbility to foster and follow directions and instructionsAbility to read, write and speak English languageMulti-tasking abilitiesDetail oriented approachUpbeat, team approachService orientedRobust communication skills and openness to learn/developWork a fixes 8-hour shift schedule Monday to Friday, but some weekend/night work, as neededUp to 5% travel, if needed to satisfy business demand Your Benefits Excellent healthcare benefits including medical, dental and visionShort and long term disability Tuition reimbursement Paid time offPet insurance Other supplemental benefits available upon election Please feel free to contact us You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future.
Together, we ensure that our patients receive professional support, hands-on guidance, and reliable delivery of essential medical supplies. We are looking to strengthen our team and are seeking a Head of Continuous Improvement (m/w/d) (Certified Master Black Belt) - 25% travel to join us.
About us Your Contribution Lead, coach, and motivate employees within respective area of responsibility, while providing direction to achieve department goals and objectivesAssist in developing department budget and investment plan(s) according to strategic goalsCultivate employee talent through training and coaching measures, while also conducting employee performance reviewsSupport the development and updating of Quality Assurance programs, policies, processes, procedures and controlsReview, analyze and report on quality discrepancies related to SCHOTT products, while developing disposition and corrective actions for product discrepanciesManage the review of batch records and avoid impacting shipment datesManage Department Training Coordinator activities and projectsManage document control activities to include, releasing, archiving, tracking and reporting of the document review process for controlled documentsLead and support the implementation of Systems and Compliance Improvements including site compliance, along with data integrity requirementsMeasure and analyze Quality System trendsOversee the internal audit function to ensure ongoing compliance to the Quality Management System (QMS)Maintain the Archive Room and document retention requirementsWrite and revise Standard Operating Procedures (SOPs) and provide training, as requiredManage the CAPA and Change-Control process to include, issuing, reviewing and approving stepsSupport all customer or registrar quality related audits and/or evaluationsUtilize quality tools, including Compliant-PRO, etc., for information, tracking and reporting purposes, as required by the Pharm Business UnitManage assigned CAPA(s) by performing root cause investigations, while defining resolution actions; implement preventive and corrective actions in a timely manner as a result of customer complaints or customer audit findingsHelp promote and implement safety/EHS directives and maintain a clean and safe workspaceAssure compliance with ISO certifications and cGMP, along with adherence to Company policies and procedures and Code of Conduct/safety guidelines Your Profile Bachelor’s Degree in Chemistry, Biology, Engineering or science related field, requiredMinimum three years of experience in Quality leadership roleSolid knowledge of ISO 9001, 14001, 15378, along with cGMP and ISOExposure to the glass forming industry and/or pharmaceutical industry, preferredThorough MS Office applications, SAP and electronic QMS systemsMulti-tasking abilitiesDecision makingDetail oriented approachForward/creative thinkingService orientedEffective communication skillsAbility to read, write and speak English language Your Benefits Excellent healthcare benefits including medical, dental and visionShort and long term disability Tuition reimbursement Paid time offPet insurance Other supplemental benefits available upon election Please feel free to contact usYour Profile Bachelor’s Degree in Chemistry, Biology, Engineering or science related field, requiredMinimum three years of experience in Quality leadership roleSolid knowledge of ISO 9001, 14001, 15378, along with cGMP and ISOExposure to the glass forming industry and/or pharmaceutical industry, preferredThorough MS Office applications, SAP and electronic QMS systemsMulti-tasking abilitiesDecision makingDetail oriented approachForward/creative thinkingService orientedEffective communication skillsAbility to read, write and speak English language
Du arbeitest eng mit Kliniken und Fachärzt/innen zusammen. Bleib dran und denke vorausschauend! Du sammelst Medical Insights, beobachtest wissenschaftliche Entwicklungen und arbeitest crossfunktional mit internen Medical-Teams zusammen. dein profil: Du hast einen Studienabschluss in Medizin, Pharmazie, Biologie oder einer vergleichbaren Fachrichtung, idealerweise mit Promotion oder Facharztausbildung?
Du arbeitest eng mit Kliniken und Fachärzt/innen zusammen. Bleib dran und denke vorausschauend! Du sammelst Medical Insights, beobachtest wissenschaftliche Entwicklungen und arbeitest crossfunktional mit internen Medical-Teams zusammen. dein profil: Du hast einen Studienabschluss in Medizin, Pharmazie, Biologie oder einer vergleichbaren Fachrichtung, idealerweise mit Promotion oder Facharztausbildung?
Du arbeitest eng mit Kliniken und Fachärzt/innen zusammen. Bleib dran und denke vorausschauend! Du sammelst Medical Insights, beobachtest wissenschaftliche Entwicklungen und arbeitest crossfunktional mit internen Medical-Teams zusammen. dein profil: Du hast einen Studienabschluss in Medizin, Pharmazie, Biologie oder einer vergleichbaren Fachrichtung, idealerweise mit Promotion oder Facharztausbildung?
Dieser absolut wichtige Teil Ihrer Aufgabe und Ihrer Verantwortung darf gerne 50% Ihrer Tätigkeiten beanspruchenProzesskonforme Dokumentation und Reviews: Sie stellen die korrekte Dokumentation unserer Software-Entwicklungsprojekte und führen regelmäßige Reviews durch.Medizinproduktakten: Die Erstellung und Pflege von Akten gemäß der Medical Device Regulation (MDR) gehört zu Ihrem know howWeiterentwicklung des QM-Systems: Ihre aktive Mitarbeit bei der kontinuierlichen Verbesserung des Qualitätsmanagement-Systems im Bereich Software-Entwicklung ist gewünscht.Cybersecurity: Zusammen mit dem Cybersecurity Experten unterstützen Sie das Team bei Sicherheitsfragen und der Umsetzung von Cybersecurity-Maßnahmen.Usability- und Risikomanagement: Sie sind aktiv an der Durchführung von Usability- und Risikomanagementaktivitäten beteiligt.
Proactive participation in all phases of software development from feasibility studies through design,development, testing and bug fixing and maintenanceCollaboration within the Scrum-TeamsIndependent interaction with internal framework manufacturersBased on requirements and models, definition of software architecture, design and specifications, ultimately leading to implementationParticipation in the definition of work packages, their estimation and planning in a sprint-based agile environmentAdherence to a software development process including contribution to written deliverables and documentation Degree in a software related field such as software or electrical engineering or similarHands-on experience as Software Engineer, preferred in the regulated environment such as the medical device industryYears hands- on experience with C++ and Linux from the last project or positionStrong with Linux DockersExperience with CAN busSoftware architecture would be advantageous Internal career opportunities World-renowned biotech company Ihr Kontakt Referenznummer 865145/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Wir entwickeln, fertigen und liefern unsere Premiumprodukte an die wichtigsten Hersteller in aller Welt in den Branchen Medical, Test&Measurement, Military, Robotics und wachsen seit über 30 Jahren sehr dynamisch. Als Technischer Projektleiter übernehmen Sie die Leitung für die Neuentwicklung und Weiterentwicklung unserer Lithium-Ionen Batterien und Ladegeräte – von der Konzeption (Software-, Mechanik- und Elektronikaspekte) bis zur Serienreife.
Dabei stellst du sicher, dass diese wissenschaftlich überprüft und angemessen referenziert werden, von hoher Qualität sind sowie den einschlägigen Verfahren des Unternehmens, des Medical Office und der lokalen Behörden entsprechen. Übernimm Verantwortung! Du verantwortest die Projektleitung in und zwischen den Teams vor Ort und im therapeutischen Bereich, einschließlich angemessener Zuweisung und Überwachung des lokalen MSL-Budgets.
Das Unternehmen bietet Raum für Menschen, die Verantwortung übernehmen möchten und Freude daran haben, an anspruchsvollen, zukunftsorientierten Technologien mitzuwirken Weiterentwicklung eines schlanken, risikobasierten Qualitätsmanagementsystems (ISO 13485, AI Act) Sicherstellung regulatorischer Anforderungen für aktive Medizinprodukte, sterile Produkte sowie Software as a Medical Device (SaMD) Vorbereitung, Koordination und Begleitung internationaler Zulassungs- und Registrierungsprozesse (EU/MDR, USA/FDA) inkl.
Das Unternehmen bietet Raum für Menschen, die Verantwortung übernehmen möchten und Freude daran haben, an anspruchsvollen, zukunftsorientierten Technologien mitzuwirken Weiterentwicklung eines schlanken, risikobasierten Qualitätsmanagementsystems (ISO 13485, AI Act) Sicherstellung regulatorischer Anforderungen für aktive Medizinprodukte, sterile Produkte sowie Software as a Medical Device (SaMD) Vorbereitung, Koordination und Begleitung internationaler Zulassungs- und Registrierungsprozesse (EU/MDR, USA/FDA) inkl.
We will need you to possess the following essential qualities and skills: Recognized Degree in IT; Computer Science; Software Engineering, Finance, Business Information Technology or relevant fieldsAbove 3.0 CGPA / Second Class upper (Hons)Less than 1-year ofworking experienceHighly self-motivated team player with good analytical and conceptual thinking, results-driven with initiative and good negotiation skillsAll rounded individual with a deep interest in IT industry who enjoys challenges and strive to work with professionals in IT industry globallyAble to quickly absorb professional knowledge, good in problem-solving, contribution and leadershipEagerness to take responsibility over complex processes and ability to multitaskExcellent verbal and written English WHAT IS THE PLUS POINT (S) Experience in self-initiated projects WHAT YOU WILL GET FROM US Great team of IT professionals with global working exposure Meal Card and Flexible Benefits – customized according to individual needs On-going professional and technical training and certifications A multicultural environment in modern offices Choose any day for your vacation from earned public holiday (Saturday and ad hoc) Smart casual everyday Global internal job opportunities available within DPDHL Unlimited Outpatient Medical Home office possibilities If you are up to the challenge, contact us today and we will ensure that you will have an experience of a lifetime.
Mein Arbeitgeber Our client is a globally recognized leader in the medical technology and diagnostics industry. The Rotkreuz site focuses on the development and testing of advanced laboratory instruments used worldwide in highly regulated environments.
Mein Arbeitgeber Our client is a globally recognized leader in the medical technology and diagnostics industry. The Rotkreuz site focuses on the development and testing of advanced laboratory instruments used worldwide in highly regulated environments.
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
Develop and maintain software solutions by applying in-depth technical knowledge and problem-solving skills, while ensuring compliance with regulatory standards for medical softwareEnsure the timely delivery of high-quality software for medical devices that meets both the company's standards and customer needs, influencing the success of the team and broader project outcomesCommunicate complex technical concepts effectively, fostering an environment of collaboration and continuous learning within and across diverse and intercultural teamsEmpower your team members to take ownership of their work and leading by example to foster teamwork and mentorship Degree or equivalent practical experience in a specialized field related to software development or engineeringProven experience in software development, with a demonstrated passion and hands-on professional experience working with Rust incl. a solid understanding of Rust's core concepts (ownership, borrowing, and lifetimes), experience with asynchronous programming in Rust (e.g., using async/await) and familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx).Capable of solving complex issues creatively and effectively, using a multi-faceted approach based on thorough analysis to resolve complex technical challengesExcellent communication skills with the ability to foster an inclusive and diverse environment as well as collaborate effectively within and across teamsEnglish fluency is a prerequisite, German is advantageous Internal career opportunitiesWorld-renowned medical devices company Ihr Kontakt Referenznummer 858105/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
What makes you stand out Proven experience in RPA development (minimum 3 years) using tools like UiPath, Automation Anywhere, or Blue Prism.Strong programming skills in languages such as C#, .NET, Java, or Python.Knowledge of software development methodologies, Agile frameworks, and version control.Experience with process mapping and business process analysis.Strong problem-solving and debugging skills.Excellent communication skills, with the ability to collaborate effectively with cross-functional teams.Bachelor’s degree in Computer Science, Information Technology, or a related field. What we offer: Attractive benefits packageRegina Maria medical subscription for you and your family according with internal policeMeal vouchersSpecial discounts for gymsAdditional days offDKV card with discount for fuel valid in 25 countriesWhen you are in the office can have free facilities like massage, fruits, coffeeFlexible working hours with home office and flextimeContinuous training and much more...
Develop and maintain software solutions by applying in-depth technical knowledge and problem-solving skills, while ensuring compliance with regulatory standards for medical software Ensure the timely delivery of high-quality software for medical devices that meets both the company's standards and customer needs, influencing the success of the team and broader project outcomes Communicate complex technical concepts effectively, fostering an environment of collaboration and continuous learning within and across diverse and intercultural teams Empower your team members to take ownership of their work and leading by example to foster teamwork and mentorship Degree or equivalent practical experience in a specialized field related to software development or engineering Proven experience in software development, with a demonstrated passion and hands-on professional experience working with Rust incl. a solid understanding of Rust's core concepts (ownership, borrowing, and lifetimes), experience with asynchronous programming in Rust (e.g., using async/await) and familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx).
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
What we offer Work in an international company with an established position on the market.High standard of work in an international corporation.Opportunities for professional and personal development.Employment based on an employment contract.A package of non-wage benefits, including medical care, Multisport cards, learning English or German.Tools necessary for work (laptop, phone, company car). We are looking forward to your application and to applicants who enrich our diverse culture!