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Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. This position is part of the Product Cybersecurity Department, an organizational unit within the company that focuses on ensuring the security of its products and services. This department is responsible for implementing, managing, and overseeing cybersecurity measures specific to the development, deployment, and ongoing support of the company's products The primary responsibility of the position involves designing, implementing, testing, and managing security measures to protect computer systems, networks, and data. The role requires a deep understanding of current and emerging cybersecurity threats, as well as the ability to develop, implement and test robust security solutions. Key Accountabilities • Perform threat modeling and design security measures on complex applications and web-based products, • Desing and implement advanced operating system hardening, • Design and implement basic networking protections such as VPNs and tunneling, • Design advanced hardening configuration of cloud solutions, • Design simple cryptography-based solutions for data privacy and integrity protection Networking/Key relationships A cybersecurity engineer interacts with different stakeholders including: • Software development to plan and execute security and privacy by design activities, • Quality assurance to plan and execute cybersecurity testing across the product life-cycle, • Service to respond to on-market cybersecurity events impacting the company's products Minimum Knowledge & Experience required for the position: The qualifications required by the position are: • Engineer, computer science or other technical degree, or equivalent work experience The required work experience by the position is at least 4 years in one of the different tracks: • Ethical hacking and penetration testing, • Product security by design, • Cloud Security operations The following work experience and qualifications are a plus: • Strong knowledge of secure coding practices and product security best practices, • Certifications such as Certified Ethical Hacker (CEH), • Solid knowledge on SW testing process and methodology, • Knowledge on relevant standards such as ISO 27001, • Knowledge of medical device regulations Skills & Capabilities: The skills and capabilities required by the position are: • Strong analytical and problem-solving skills to identify and address security challenges and vulnerabilities, • Effective communication skills to convey complex cybersecurity concepts to both technical and non-technical stakeholders, • Willingness to stay updated on the latest cybersecurity trends, threats, and technologies through continuous learning and professional development, • Ability to collaborate with cross-functional teams, share information, and work together to enhance overall cybersecurity posture What we offer: • A meaningful project that will impact the quality of laboratory software medicine worldwide, • 3 days a week working from home, • Multicultural and friendly team, • Exciting opportunities for professional development., • Ongoing training, • Social benefits: Canteen, nursery check, continius training, Doctor at the office, retirement plan..., • All the benefits according to the chemical agreement Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V. Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics JOIN US!

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. The Senior SW Development Engineer, develop a role as as either full-stack or front-end or back-end , being involved in all stages and all areas of software development, including Test as well as architecture design, code review, and internal tool management. The programming language required for this project is Standard C++ They are responsible for developing and implementing front-end and/or back-end software applications, including back-end design, testing, and systems integration. Key Accountabilities • Performs software engineering activities including software requirements, architecture, design, implementation and test independently., • Lead software development activities within projects at technical or at project level., • Developing SW following company procedures. Able to complete somewhat ambiguous problems and defect fixing with its corresponding test., • Works across the-full stack, or focused in back-end or front-end, building scalable solutions that drive positive user experiences and measurable business impact, • Develops new software features and infrastructure elements in support of priority business and solution requirements., • Ensures application performance, uptime, risk mitigation, scalability, and high code/application quality, • Uses agile engineering practices and various software development technologies to rapidly develop creative and efficient solutions that enhance the organization’s technology stack, • Collaborates with other squad members to implement user stories, write tests, and continuously deliver new/improved product functionality., • Will design and build software that is simple and scalable. Will write maintainable code., • Will be able to Able to review and give feedback for technical and architecture documentation., • Will know your project in a low complexity level, enough to cover your work autonomously and the environment where it works with some detail., • Will work in a project with low or medium complexity, • Will able to work autonomoslly, however you know when you have to consult the experts on the issues that appear on the projects Education: Engineer, computer Science or other Technical degree, or equivalent work experience Experience: • Approximately 5-7 years of related experience, • Experience in Software Medical Devices development that follows ISO 13485 is a plus, • Proficient in all the languages and frameworks used in the project, • Proficient in Database Queries and Database Design Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and competencies: • Understand the impact of a feature. You break this down into associated tasks. You deliver frequently and predictably., • Understand your dependencies and their limitations., • Highly organized and detail-oriented, with the ability to multi-task., • Proactivity, but still work well in a team oriented environment., • Strong communication skills with the ability to communicate complex technical concepts and align the organization on decisions., • Flexibility and adaptability to a fast changing environment, • Sound problem-solving skills with the ability to quickly process complex information and present it clearly and simply, • Utilizes team collaboration to create innovative solutions efficiently, • A meaningful project that will impact the quality of laboratory software medicine worldwide, • 3 days a week working from home, • Multicultural and friendly team, • Exciting opportunities for professional development., • Ongoing training, • Social benefits: Canteen, nursery check, continius training, Doctor at the office, retirement plan..., • All the benefits according to the chemical agreement Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V. Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics JOIN US!

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Immunoassay business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Within a medical device environment, work with the QARA Manager to ensure regulatory compliance and certification of software products. Key Accountabilities Be a key part of a team where you will: • Collaborate in maintaining the quality system documentation processes and procedures adopted by the company., • Investigate and resolve quality issues, implementing corrective and preventive actions to mitigate recurrence., • Coordinate and support the preparation of software technical documents appropriate for regulatory submissions., • Support the regulatory submissions for market authorization for medical device products., • Conduct internal assessments and audits to identify areas for improvement and ensure adherence to established procedures., • Facilitate the approval process for software releases., • Disseminating knowledge about the Quality System and regulatory requirements., • Review Promotional and advertising materials., • Oversee post-market surveillance activities related to medical device products., • Offer guidance and mentorship to QARA team members at lower levels Networking/Key relationships The main relationships within to the Werfen Group are: • QARA Manger, QA Leads, Validation Led, • Factory Lead and Solution Leaders, • Customer, • Application Lifecycle manager (ALM), • Notified Bodies and Competent Authorities for product regulatory compliance., • This position may also require also cooperating with other companies inside Werfen. Minimum Knowledge & Experience required for the position: • Engineer, computer Science or other Technical carrier, or equivalent work experience., • A minimum of 3 years experience in Quality Assurance or Regulatory related, preferably within the Healthcare sector, • Additional Skills/Knowledge:, • Knowledge and experience working with medical device international regulations and related standards (ISO 13485, ISO 14971,..)., • Knowledge and experience working in Medical device software life cycle process (IEC 62304), • Desirable:, • Knowledge and experience working in medical device regulatory submissions (MDR/IVDR,FDA..), • Internal auditor qualification for management systems or knowledge of auditing techniques Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and competencies: • Good level of Technical and Conversional English., • Team player with ability to work independently., • Excellent and effective written and verbal communication skills., • Excellent interpersonal skills, good judgment and analytical skills., • Effective time management and organizational skills What we offer: • A meaningful project that will impact the quality of laboratory software medicine worldwide, • 3 days a week working from home, • Multicultural and friendly team, • Exciting opportunities for professional development., • Ongoing training, • Social benefits: Canteen, nursery check, English training..., • All the benefits according to the chemical agreement Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics JOIN US!

Acompanyar l’equip de consultors/es de selecció de l’oficina que gestionaran el procés de selecció de perfils de principi a fi: comprensió de les necessitats del client, publicació de la vacant, cribratge de CV’s, entrevistes telefòniques i presencials i interpretació de tests psicotèc

Implementación de soluciones técnicas para aumentar la eficiencia operativa.

Informatica (PowerCenter y/o Informatica Cloud). ETL Informatica (PowerCenter y/o Informatica Cloud). Udemy, certificaciones oficiales gratuitas de Azure, AWS, Google, IBM, Informatica.

We are looking for a Software Developer with experience in IT projects and advanced knowledge in Informatica PowerCenter. Develop, implement, and maintain IT solutions using Informatica PowerCenter. At least 3 years of experience with Informatica PowerCenter.

Informatica (PowerCenter y/o Informatica Cloud). ETL Informatica (PowerCenter y/o Informatica Cloud). Udemy, certificaciones oficiales gratuitas de Azure, AWS, Google, IBM, Informatica.