Informatika állások, munkák minőségbiztosítás kategóriában

Szoftverfejlesztési minőségbiztosítási feladatok (Sw QA) •Részvétel szoftverfejlesztési folyamatok minőségbiztosításában (ISO 9001, ISO 22163, EN5012x alapok) •Fejlesztési mérföldkövek (Quality Gate ek / milestone-k), dokumentum review-k QA támogatása Hardverfejlesztési minőségbiztosítási feladatok...

• Own and manage fuel card-related processes across 3 regions and 9–12 MOL countries, ensuring standardization and alignment with group-level operational standards.
• Drive strategic alignment of fuel card processes with MOL Group’s business objectives and digital transformation goals.

• Documentation Control: Maintaining, updating, and controlling quality manuals, procedures, and records.
• Audit Management: Conducting annual internal enterprise operating system (EOS) and VDA audits. Coordinating external certification audits like IATF.

• Engage with the local business and associates toward the effective promotion of organizational goals.
• Proactively identify and work through obstacles that may hinder associates from focusing on and delivering their individual impact goals.

• Contribute to mass production (SVS) projects
• Manage CRs related to the role’s scope
• Create and maintain product descriptions and compositions
• Develop and update risk management files
• Ensure Design Control in close collaboration with QA functions
• Create and maintain specifications

Lab IT Administrator Solvias is a global provider of chemistry, manufacturing, and control (CMC) analytics to the life sciences industry. Our expert team combines decades of experience with regulatory expertise across small molecules, biologics, and cell and gene therapies. Solvias offers...

Responsibility for the sustainable and timely certification and approvals of devices across four Business Units—particularly in the areas of diamond drilling and cutting, dust management, measuring and fastening tools with various drive systems, robotics, as well as wireless and IT products...

• Planning and initiation of business cases, definition of the project scope, objectives and deliverables. This includes gathering requirements, assessing feasibility and developing a project plan that aligns with organizational goals
• Monitoring of timelines and budget

Quality Assurance Engineer (limited contract from May 1st, 2026 to January 31st, 2027) Our company is further expanding by setting up a brand-new manufacturing site located in Nidau. Due to our company’s continued growth and expansion, we are recruiting a professional for the position as Quality...

Quality Assurance Engineer (limited contract from May 1st, 2026 to January 31st, 2027) Our company is further expanding by setting up a brand-new manufacturing site located in Nidau. Due to our company’s continued growth and expansion, we are recruiting a professional for the position as Quality...

Lab Technician Product Validation BÜHLMANN Laboratories AG is an internationally operating Life Science company that supports clinical laboratories with innovative diagnostic products and first-class services, empowering healthcare providers to deliver more accurate diagnostics for patients...

• Develop and implement quality management strategies and policies to ensure compliance with industry standards and regulations.
• Develop the company's Quality Management System to ensure it conforms with the customer, ISO 9001, ISO 14001, IATF16949, and regulatory/legal requirements.

Join our network As a leading Swiss company in the cable industry, we have made an excellent reputation worldwide with a comprehensive range of products and services as well as customer-specific system solutions for energy transmission and distribution. In this role you are responsible for the...

• You are responsible for quality related topics like change control, deviations and/or complaints related to DS products at CMOs
• Define together with the CMO effective CAPAs and track the timely implementation

• Host audits and inspections, ensuring compliance with internal and regulatory requirements
• Manage and support GMP/GCLP procedures, including qualification and periodic review of facility equipment
• Support vendor qualification procedures and maintain related documentation as needed