Junior software developer állások Külföldön (minőségbiztosítás)

Betreuung, Implementierung und Überprüfung von Maßnahmen zur Qualitätssicherung unter Anwendung der etablierten Q-Systeme. Sie stellen Quality Oversight im Plasmacenter sicher....

Description: ACTIVITIES * Executes the general cleaning of the manufacturing area in a clean room environment * Disinfection of materials before introducing them into clean rooms * Compile GMP documentation related to general cleaning * Cooperating and working with the manufacturing team according...

• Ensure each site supports effective CAPA implementation and continuous improvement.
• Lead the CAPA Review Board to drive alignment with quality goals and expectations across the organization.

• Driving supplier performance improvement through root cause analysis, corrective action and supplier performance reviews;
• Ensure compliance with the European Medical Device Directive and associated regulations;

• Maintain and further develop our QMS in line with EN ISO 13485 and MDSAP
• Create, update, and improve procedures, forms, and training materials
• Plan and deliver training on procedures and regulatory requirements
• Lead and oversee CAPA initiation, processing, tracking, and review

• Establish and maintain the fire safety management system
• Conduct fire risk assessments for factories and battery energy storage warehouses
• Develop and update fire prevention and emergency response plans

Performing wet chemical, instrumental, or bioanalytical methodsfor in-process controls, release and stability testing for raw and starting materials, intermediates, as well as consumables and packaging materials according to test instructions/protocols...

• Provide theoretical and practical support for the installation of SAFRAN engines in the helicopter manufacturer's final assembly line
• Issue and manage airworthiness certificates, including the maintenance and update of engine logbooks

Proactively develop and implement the quality strategy for the assigned components group, aligning it with long-term business goals and engaging with cross-functional stakeholders globally....

• Support development projects at transfer or validation level by executing laboratory work
• Perform immunological tests using various platforms (e.g., Flow Cytometry, ELISA, PETIA, etc.)
• Conduct studies to establish and optimize kit reagents and protocols

• Steuerung und Leitung der Produktionsbereiche: Rohfertigung, Verpackung und Logistik mit 200 Mitarbeitenden
• Verantwortung für das Tagesgeschäft, insbesondere für die Sicherstellung von Qualität, Termintreue und Wirtschaftlichkeit

• You support us in the process of product development
• You help us in project follow up to prepare the product launch
• You assist to organize benchmarking activities
• You participate in communication with clients and countries

• Guiding and supporting your team by overcoming roadblocks and exceeding expectations
• Ensuring appropriate staffing for all active Simultaneous Development Teams (SDTs) in collaboration with Program Management and Quality leadership

• Review customer specifications and legal/statutory requirements, ensuring compliance with Voith Hydro standards and EQM guidelines.
• Prepare and issue project-specific Quality Plans and documentation (e.g., Inspection & Test Plans, QS, MGS).

• Lead global manufacturing quality strategy, ensuring alignment with Voith Hydro's renewable energy objectives.
• Ensure quality oversight across diverse manufacturing processes, with a strong focus on turbine and generator fabrication.

• Support and assist internal and external customers with technical inquiries
• Provide on-site technical consulting in Suisse romande, France, and occasionally in other European regions
• Support customers with product launches, system settings, application trials, and quality assurance measures

• Conduct HPLC analyses for release and stability testing of small molecules and professional use of various HPLC separation techniques.
• Work collaboratively on method validation and verification to support drug development program
• Data interpretation and exploitation in CDS

• Timely commissioning and qualification of laboratory equipment
• Independent commissioning of equipment, including handling repairs and accompanying external service providers
• Assigning, handing over, and returning laboratory equipment to internal customers and external services

• Produce, scale up, and quality-control our MUSE kits and reagents.
• Purify oligonucleotides, proteins, and DNA; perform conjugation protocols.
• Prepare buffers and chemical reagents with precision.
• Assemble kits and execute QC protocols according to ISOcompliant standards.

Project & Process Quality Assurance: You define and implement quality assurance strategies across the entire product lifecycle - from suppliers and development to serial production....