Junior Pavement Inspector

Join SGS as a Regulatory Elevator Equipment Inspector in Madrid. In this pivotal role, you'll be responsible for ensuring compliance with safety standards and regulations governing elevator systems. Your expertise will help maintain the highest safety standards in the industry, ensuring the reliability and safety of elevator equipment.

Join SGS as a Junior Inspector for Gas Vehicles and Pressure Equipment, where you will play a crucial role in ensuring safety and compliance in the field. In this full-time position based in Madrid, you will conduct inspections and assessments, contributing to our commitment to quality and excellence. Your expertise will help maintain high standards and foster safe practices in the industry.

Join our dynamic team at SGS as a Junior Inspector specializing in Gas Vehicles and Pressure Equipment. In this pivotal role, you will be responsible for conducting inspections and ensuring compliance with safety regulations. You will work closely with experienced professionals in the field, gaining invaluable insights and expertise in vehicle and equipment assessment.We seek a motivated individual who is passionate about safety and quality assurance. This is a fantastic opportunity to further your career within a globally recognized company.

Miratech is seeking a Telecommunications Regulatory Auditor based in Madrid. This position plays a key part in maintaining compliance with telecommunications laws and industry standards. Role overview The Telecommunications Regulatory Auditor conducts audits focused on regulatory compliance. The work involves reviewing internal practices, evaluating current frameworks, and checking that operations align with legal requirements. What you will do Carry out compliance audits for telecommunications activities Assess regulatory frameworks and identify any gaps or risks Recommend and help implement solutions to address compliance issues Support efforts to uphold Miratech’s reputation for meeting industry standards Location This role is based in Madrid.

At SGS, we invite you to embark on a professional journey with us, fostering your growth in an international and multidisciplinary environment. Are you ready to join a leading company in the industry?We are currently seeking a Regulatory Environmental Technician for our Madrid office:Your responsibilities in this role will include:Conducting functional tests on continuous measuring devices (SAM).Sampling and testing atmospheric emissions.Recording and classifying results based on established criteria.Managing relevant legislation and regulations within the sector.Organizing and maintaining the equipment necessary for inspections.

Envision this... As a Quality Inspector, you will be immersed in a dynamic production environment, surrounded by groundbreaking defense aerospace technologies — components engineered to conquer the skies, endure harsh conditions, and enhance future defense systems. You serve as the vital checkpoint ensuring that innovation meets unwavering reliability. At Destinus, we are pioneering advancements in the defense sector with our state-of-the-art Unmanned Aerial Vehicles (UAVs). Our groundbreaking technologies are crafted to fulfill the distinct requirements of contemporary defense missions, providing unmatched speed, accuracy, and cost efficiency. Destinus collaborates with government bodies and defense organizations globally to deliver superior solutions for mission-critical tasks, heralding a new age of operational efficiency and technological dominance. Join us in redefining the future of defense through revolutionary aerospace innovations.Your Role Quality Guardian - Inspect aerospace components, assemblies, and processes to ensure compliance with standards — no compromises allowed. Root Cause Solver - Detect defects, analyze root causes, and collaborate closely with production and engineering teams to rectify issues before they escalate. Quality Enhancer - Contribute to the enhancement of our inspection processes, discovering smarter and quicker methods to uphold top-tier quality without hindering progress. Results Documenter - Log inspection outcomes and create reports — quality for us is not just a practice, it's a commitment we substantiate. Essential SkillsRequired QualificationsMust-Have Demonstrated experience as a Quality Inspector in aerospace, automotive, or advanced technology manufacturing. Strong comprehension of technical drawings, blueprints, and inspection methodologies. Exceptional attention to detail — you can identify flaws that others might overlook. Familiarity with ISO standards, quality management systems, and reporting protocols. Proficient in English – it is our primary working language. Willingness to adapt to a rotating morning-afternoon shift schedule weekly. Working hours - 7:00 AM to 3:00 PM for morning shift; 2:00 PM to 10:00 PM for afternoon shift. Preferred Qualifications Experience with non-destructive testing (NDT). Familiarity with Lean Manufacturing or Six Sigma methodologies. Basic knowledge of composite materials or advanced alloys. Who You AreYou are not merely an inspector — you are a detail-oriented perfectionist driven by purpose. You excel in fast-paced, high-stakes environments where every minor detail has significance, motivated by an innate curiosity to constantly seek improvements in efficiency and effectiveness. As a proactive problem solver, you don’t just identify issues — you delve into them, ascertain the root cause, and collaborate to implement solutions. Most importantly, you are passionate about ensuring the highest standards of quality in everything you do.

Role Overview Eurofins Scientific is hiring an Equipment Qualification Technician for its Madrid location. This position plays a key part in the pharmaceutical sector, focusing on equipment validation and compliance. What You Will Do Verify that equipment used in pharmaceutical processes meets required quality and compliance standards Support the validation and qualification of new and existing equipment Help maintain high standards for product quality by ensuring equipment reliability About Eurofins Scientific Eurofins Scientific is committed to delivering high-quality products through rigorous quality controls and continuous improvement in the pharmaceutical industry.

Join AbbVie as a Regulatory Manager specializing in labeling for medical devices. In this temporary role, you will oversee compliance with regulatory requirements while ensuring the accuracy and clarity of product labeling. Your expertise will contribute to the successful launch and market presence of our innovative medical products.

Join us on an exciting journey as we tackle real-world challenges in the field of AI diagnostics!At SpotLab, we are at the forefront of AI innovation, empowering biopharmaceutical research and diagnostic advancements with our state-of-the-art AI solutions. As a burgeoning startup specializing in AI-driven medical diagnostics, we seek a talented individual who can enhance our processes and adeptly navigate regulatory landscapes to achieve compliance.With a strong foundation in quality and regulatory affairs, SpotLab has achieved significant milestones, including acquiring the In Vitro Medical Device Manufacturer License from the Spanish Medicines Agency, establishing a Quality Management System compliant with ISO 13485 standards, securing CE Marking for two AI diagnostic products under the IVDD, and obtaining ISO 27001 certification. We are committed to evolving our regulatory approach to keep pace with the dynamic landscape.In this role, you will have the opportunity to make a meaningful impact by helping to certify AI models for microscopy images in hematology and infectious diseases, ultimately transforming patient care on a global scale.SpotLab has garnered over 10 international awards, including the prestigious Seal of Excellence from the European Union. Our multidisciplinary team champions gender parity and brings together professionals from diverse backgrounds, including engineers, medical doctors, clinical researchers, and business strategists.

Ascendis Pharma develops therapies for rare endocrinology and oncology conditions, using its proprietary TransCon® technology platform. With headquarters in Denmark and offices across Europe and the United States, the company focuses on addressing unmet medical needs and is committed to patient care and scientific innovation. Role overview The Pharmaceutical Affairs Manager oversees pharmaceutical operations for Spain and Portugal, ensuring full compliance with Spanish, Portuguese, and EU regulatory standards. This position supports quality management, pharmacovigilance, and manages regulatory interactions with local authorities. The manager also assists with quality processes and tender management. This role involves frequent collaboration with local teams in Sales, Market Access, Medical Affairs, Compliance, and Finance, as well as global colleagues in Legal, Quality, Regulatory Affairs, and Supply Chain. The position reports to the General Manager for Iberia and is based in Madrid. Presence in the office is required at least three days per week, with flexibility for remote work on other days. Main responsibilities Supervise regulated activities, including distribution, storage, import/export, promotional materials, medical information, and quality documentation. Ensure compliance with pharmaceutical laws in Spain and Portugal, and adhere to local and EU regulations (GDP, GMP, GVP, MDR). Review documentation related to pharmaceutical operations, distribution, and product handling. Assist with preparation and submission of local regulatory documents, including variations and notifications. Facilitate submission of materials for pre-approval to local authorities as needed. Support administrative tasks related to regulatory documentation, such as Certificado de Exclusividad. Quality management Assist with local implementation of the Ascendis Quality Management System. Act as the QA/compliance contact for the local affiliate, working with the global QA team. Other quality-related tasks as required.