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Within IT GFS SAP Platform, as jobholder you will be working in the ERP+ Operations Team. This includes responsibility for SAP Basis security, governance and operational stability. Please note: The job title used in this advertisement may differ from the official contractual title. • Consulting, development and implementation of SAP security concepts (e.g. Network segmentation, application and database levels, SAP Message Server, ACL- Access control list), • Conception, development and implementation of the communication architecture (load balancer, SAP Web Dispatcher, SAP Gateway, HTTPS, Certificate, SNC‑Secure network communications), • Firewall rules log analysis and definition of rules, • Transfer of the new security requirements into the rules and regulations, • Execution of SAP Security Audits and vulnerability analyses in the SAP infrastructure, • Experience in monitoring Focused Run and predictive analytics, • Participation in penetration tests, • Understanding of social engineering or other hacking methodologies / best practices, • Knowledge in artificial intelligence is a plus, • You will work in an international environment within the global IT department, • Bachelor's or master's degree in IT or similar studies, • 4 years experience working in IT Basis Security, • Deeply familiar with ERP Basis security management tools and how to best utilize them for optimal protection, • Excellent knowledge in GxP compliance and documentation practices, • Experience in global stakeholder and project management, • Proven ability to work creatively in a business and technical environment to contribute global IT strategies and realization plans, • Fluent in English with excellent communication and intercultural competencies, • Flexible working conditions, • Life and accident insurance, • Health insurance at a competitive price, • Investment in your learning and development, • Gym membership discounts #J-18808-Ljbffr

Process Engineer At Anaconda Biomed, we are seeking a motivated Process Engineer to develop, optimize, validate, and transfer manufacturing processes for innovative medical devices. You will help scale and improve manufacturing processes, support technology transfers from R&D to Production, lead continuous improvement initiatives, and ensure compliance with quality and regulatory requirements. Experience in a regulated environment is required, with preference for candidates from the Medical Device industry or the pharmaceutical, biotechnology, or healthcare sectors. An advanced level of English is required, both written and spoken. English is regularly used for internal and cross-functional meetings, international collaboration, training, and technical documentation. Key Responsibilities - Design, develop, optimize, and validate manufacturing processes. - Support technology transfers from R&D to Production. - Analyze process performance and identify improvement opportunities. - Define, control, and monitor critical process parameters. - Design and execute process characterization studies and Design of Experiments (DoE). - Support process validation and equipment qualification. - Investigate deviations and non-conformities and support corrective and preventive actions. - Collaborate with Production, Quality, R&D, Regulatory Affairs, and Supply Chain teams. - Prepare and maintain technical documentation in line with Quality Management System requirements. - Support continuous improvement projects using Lean Manufacturing, Kaizen, TPM, and 5S methodologies. - Define, monitor, and analyze KPIs related to quality, efficiency, and process performance. - Support the implementation, commissioning, and optimization of new manufacturing equipment and technologies. - Ensure compliance with internal procedures and applicable regulatory requirements. Requirements - Bachelor’s degree in Mechanical, Industrial, Biomedical, or Chemical Engineering, or a related field. - Experience in manufacturing or industrial environments. - Experience supporting process improvement and manufacturing optimization projects. Preferred Qualifications - Experience in the Medical Device industry. - Experience working under regulated quality systems, such as ISO 13485, GMP, or equivalent. - Experience in medical devices, pharmaceuticals, biotechnology, healthcare, or another highly regulated sector. - Experience with process validation and equipment qualification. - Experience managing CAPAs, non-conformities, and change controls. - Practical experience with Lean Manufacturing and continuous improvement methods. - Experience with Design of Experiments (DoE) and statistical analysis. Technical Knowledge - Process optimization and manufacturing process control. - Process validation principles. - Analytical and statistical techniques. - CAD tools, preferably SolidWorks or similar software. - Lean Manufacturing, Kaizen, TPM, and 5S methodologies. - Quality management systems and regulated documentation. Languages Spanish and English — Advanced level required (C1 or equivalent) You should be comfortable with: - Participating in internal and cross-functional meetings in English. - Attending and contributing to training sessions in English. - Communicating with international teams and global stakeholders. - Drafting and reviewing technical documentation in English. Ideal Candidate Profile You understand the importance of quality, traceability, documentation, and regulatory compliance in daily operations. Experience in medical device companies or other regulated environments is highly valued, particularly experience with process validation, document control, change management, regulatory compliance, and quality systems. The ideal candidate combines a strong engineering background, a continuous improvement mindset, effective communication skills in English, and experience working within the quality standards and regulatory requirements of highly regulated industries.

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