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1668 Ergebnisse

1668 Ergebnisse

    Referenznummer: 873927/1

    Quality Assurance Engineer (m/f/d)

    Arbeitnehmerüberlassung
    Urdorf
    • Manage Change Requests, CAPAs, and Non-Conformities
    • Execute established workflows for biotech development projects
    • Act as a key contact for all quality-related topics within the project team
    • Perform risk and hazard analyses, including FMEA
    • Conduct incoming inspections, in-process controls, and FATs
    • Maintain and manage the electronic Document Management System (eDMS)
    • Support the implementation of a supplier management process
    Online seit: Mon May 11 15:14:23 CEST 2026
    Referenznummer: 871465/1

    Quality Assurance (m/f/d)

    Arbeitnehmerüberlassung
    Erlangen
    • Support the Project Manager and Application Manager in activities related to the development and/or implementation of the software-specific quality activities in projects or changes
    • Act as Quality Assurance review of Project documentation to comply with quality rules e.g. ensure that software tests are appropriately documented and defects are tracked and retested
    • Review and Approval of IT Software Change documentation mainly for SAP Systems and also other IT software
    Online seit: Wed Apr 22 15:10:31 CEST 2026
    Referenznummer: 871239/1

    Python Software Developer – Forecasting & Analytics | Aircraft Engine Services (m/f/d)

    Arbeitnehmerüberlassung
    Berlin
    • Design, develop, deploy and maintain software solutions addressing business challenges in the aircraft engine services domain
    • Build and enhance our forecasting and analytical capabilities to deliver industry-leading tools with transformational business value
    • Apply and promote software development best practices, including clean code, testing, documentation and CI/CD
    • Collaborate closely with cross-functional teams in an agile environment
    Online seit: Wed Apr 22 11:48:04 CEST 2026
    Referenznummer: 867205/1

    Sr. EHS Specialist - Cell (m/f/d)

    Arbeitnehmerüberlassung
    Grünheide
    • Preparation of risk assessments, operating instructions, and training materials
    • Inspections of battery cell production and organization of air quality measurements
    • Consulting on hazardous substances regulations and technical rules for workplaces
    • In these topics integrated are as well the topics HazMat, industrial hygiene, hoisting and lifting, building installations, machine safety, electrical safety, LOTO, confined space entry, Cathode, analyzing incidents and implementing corrective actions
    Online seit: Fri Mar 20 12:05:05 CET 2026
    Referenznummer: 866274/1

    Incident/Emergency Response & Legal/Compliance Liaison (m/f/d)

    Arbeitnehmerüberlassung
    Bavaria
    • Continuously map, monitor, and embed applicable compliance obligations into the Security Incident & Emergency Response workflow through close coordination with internal and external stakeholders
    • Facilitate case-specific compliance gap analyses during incidents, liaising with the relevant stakeholders to guarantee that regulatory and policy obligations are met
    • Engage throughout every phase of security incident and emergency response, tailoring your involvement to each situation while keeping technical, regulatory, and public-relations factors in sync. Take charge of low-level incidents
    • Support the maintenance and expansion of a collaborative ecosystem with external entities to build long-term, stable security partnerships
    • Work with systems and procedures that identify potential security incidents, such as SIEM tools, threat intelligence, or alerts
    • Your role concentrates on the consumer-electronics sector, such as mobile phones and wearable devices.
    Online seit: Tue Mar 17 09:00:00 CET 2026
    Referenznummer: 865508/1

    Regional KOL Senior Manager (m/f/d)

    Arbeitnehmerüberlassung
    München
    • Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectives
    • Design and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regions
    • Build and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutions
    • Conduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiatives
    • Contribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical data
    • Oversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL Director
    • Act as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentation
    • Plan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical Officer
    • Represent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencers
    • Serve as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic community
    • Collaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities
    Online seit: Tue Mar 10 15:12:15 CET 2026
    Referenznummer: 819257/1

    Automation Engineer (m/f/d)

    Arbeitnehmerüberlassung
    Lake Constance
    • Maintenance Responsibilities:Perform preventive and corrective maintenance on equipment and automation systems and Diagnose technical failures and implement solutions to ensure operational continuity and Document all maintenance activities and update maintenance records
    • SCADA Systems Management: Monitor and maintain SCADA systems from IMA, GEA, Sartorius, Ortner and Groninger and Update and modify SCADA programs as necessary for improvements and production requirements and Ensure the integrity and security of SCADA systems in accordance with company policies 
    • Pharmaceutical Automation Knowledge: Familiarity with GAMP5 (Good Automated Manufacturing Practice) for the validation of automated systems and Expertise in pharmaceutical manufacturing environments and GxP (Good Practice) requirements, including GMP (Good Manufacturing Practice) and Experience in maintenance and operation within controlled environments, including clean rooms
    • Documentation and Compliance: Maintain comprehensive maintenance and software change documentation in compliance with regulatory standards and Act as SME and attend validation reports, qualification protocols (IQ/OQ/PQ), and internal and external audits and Ensure all activities comply with local and international regulatory requirements
    • Data Management and Reporting: Analyze operational data collected by SCADA systems to identify trends and improvement opportunities and Generate detailed technical reports on system performance and corrective actions taken and Collaborate with quality and production teams to ensure conformity with regulatory standards
    • Training and Technical Support: Train operators and maintenance technicians on the proper use of SCADA systems and PLCs, over specific demands and Provide real-time technical support to resolve operational issues and minimize downtime and Conduct continuous training sessions to update teams on new technologies and maintenance practices
    • Optimization and Continuous Improvement: Create or review Audit Trail Reviews (ATR) on ongoing projects, as per company standards and Create or review Standard Operating Procedures (SOP’s) and Propose and implement continuous improvement projects aimed at increasing efficiency and reducing operational costs and Participate in cross-functional teams to develop innovative solutions to automation challenges and Perform periodic audits of automation systems to ensure optimal performance
    • Compliance and Safety: Ensure all maintenance and automation activities comply with safety standards and pharmaceutical regulations and Actively participate in the company’s safety and quality programs and Investigate and report any incidents or near misses related to automation and implement preventive measures
    Online seit: Wed May 28 14:38:52 CEST 2025
    Referenznummer: 821921/1

    Clinical Trial Associate für den Bereich Quality Assurance (m/f/d)

    Arbeitnehmerüberlassung
    Greater Frankfurt area
    • Quality Oversight & Systems Management: Monitor compliance with quality guidelines in clinical business areas and implement regional quality plans
    • Identify potential gaps, recommend solutions, and escalate relevant issues
    • Assist in maintaining and improving quality documents and processes
    • Audit & Inspection: Lead and support audit and inspection preparations, including document management and response coordination
    • Ensure trial sites and teams are inspection-ready
    • Consultation & Collaboration:Serve as the primary quality consultant, providing guidance on regulatory requirements and risk management
    • Support root cause analysis, CAPA processes, and audit planning
    • Collaborate with quality teams to strengthen quality culture and resolve issues
    • Process Improvement & Metrics: Drive continuous improvement and process optimization
    • Analyze quality metrics to identify gaps and recommend corrective actions to enhance compliance and efficiency
    Online seit: Mon May 19 16:25:09 CEST 2025

     

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