Regulatory Elevator Equipment Inspector

At Suade Labs, we provide intelligent, data-driven SaaS solutions tailored for the financial industry. Our innovative platform empowers clients to achieve regulatory reporting compliance, gain profound business insights, and swiftly adapt to regulatory changes.We are seeking a Senior Delivery Manager who will spearhead intricate, multi-jurisdictional regulatory reporting implementations. This senior client-facing position demands excellent judgement, a disciplined approach to delivery, and the capability to guide both clients and internal teams throughout the entire project lifecycle. You will oversee several implementations, mentor junior delivery managers, and play a pivotal role in enhancing our delivery methodologies.Suade is proud to be an equal opportunity employer. All qualified candidates will be considered without bias.Please note that we cannot provide visa sponsorship for this position.

Veeva Systems is a visionary organization at the forefront of the industry cloud, dedicated to accelerating the delivery of therapies to patients within the life sciences sector. As one of the fastest-growing SaaS companies globally, we achieved over $2 billion in revenue in our most recent fiscal year, with substantial growth opportunities on the horizon.Our core values at Veeva include: Do the Right Thing, Customer Success, Employee Success, and Speed. We made history in 2021 by becoming a public benefit corporation (PBC), which legally commits us to balancing the interests of our customers, employees, society, and investors.As a Work Anywhere company, we promote flexibility, allowing you to work from home or in an office setting that best suits your needs.Join us in transforming the life sciences industry, where we are dedicated to making a positive impact on our customers, employees, and communities.Position OverviewVeeva Systems is seeking dynamic individuals with consulting and system implementation expertise, who are passionate about helping clients enhance their regulatory data and document management processes.Our Vault RIM suite is the only integrated software solution in the industry that offers comprehensive regulatory information management (RIM) capabilities, encompassing data management, document management, submission publishing, and archival functions all on a single cloud-based platform.As part of our Professional Services team, you will be instrumental in understanding our clients' global regulatory requirements, translating these needs into effective solution designs, and configuring our cloud-based platform to manage regulatory information across their organizations.This position is fully remote for candidates located in the EU/UK, provided they are near an airport and can meet travel requirements. We encourage qualified candidates from the EU/UK to apply.

Join our innovative team at docplanner as a Senior Healthcare Regulatory Specialist specializing in software as a medical device (saMD). This remote-friendly position based in Spain offers you the opportunity to leverage your regulatory expertise to ensure our products meet the highest standards of compliance. You will play a crucial role in navigating the complex landscape of healthcare regulations, working with cross-functional teams to streamline processes and safeguard patient safety.

Role overview SGS is hiring a Senior Regulatory Inspector with a focus on mechanical areas for the Sant Joan Despí location. This position involves carrying out detailed inspections, verifying compliance with regulatory standards, and offering consulting within the mechanical sector. The role plays a key part in upholding SGS’s industry reputation for reliability and quality.

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.

Role overview The Regulatory Inspector Engineer position at SGS centers on ensuring compliance with applicable regulatory standards. The role plays an important part in promoting safety and quality across a range of sectors. Key responsibilities Carry out inspections to confirm that operations meet regulatory requirements. Contribute to efforts that sustain high levels of safety and quality. Work closely with colleagues who prioritize regulatory compliance. Location This role is located in Irún.

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.

At SGS, the world's leading inspection, verification, testing, and certification company, we believe our greatest asset is our people. We are committed to professionals who embody integrity, curiosity, excellence, respect, inclusion, and collaboration. Our unique culture fosters an environment where you can thrive, innovate, and develop alongside an exceptional team.Are you ready to elevate your career by joining a sector-leading company? We want to meet you!We are currently seeking an Electrical Engineer for the role of Authorized Control Body Inspector (OCA).You will join our technical team and play a crucial role in ensuring the safety, quality, and compliance of industrial installations. Your main responsibilities will include: Field Work in Industrial InstallationsConducting regulatory OCA inspections on low and high voltage electrical installations.Verifying compliance with current regulations and identifying potential deviations or risks.Providing basic technical advice to clients during visits. Technical and Document ManagementPreparing detailed technical reports following inspections.Managing and tracking reports, evidence, and associated documentation.Ensuring compliance with the internal procedures of the Authorized Control Body. Client Interaction and Team CollaborationDirect contact with clients for technical clarifications and inspection planning.Coordinating with your team to ensure efficient and high-quality execution of work.Continuous learning and participation in internal training to grow as an OCA professional.

Precision for Medicine is a global Clinical Research Organization with a focus on advancing precision medicine. The team works across rare diseases, oncology, and other therapeutic areas, combining clinical trial design, operational and medical expertise, and biomarker-driven data analytics. The company is expanding and seeks a Regulatory and Start-Up Specialist based in Spain. This remote role calls for experience in contracts and budgeting negotiations within the Spanish clinical research landscape. What You Will Do Drive site activation readiness for assigned countries and sites, monitoring progress and addressing risks before they impact timelines. Prepare and submit Clinical Trial Application Forms and dossiers (including amendments and notifications) to Competent Authorities, Ethics Committees, and other local bodies, following Spanish regulations and deadlines. Communicate with Competent Authorities and Ethics Committees to address study-related questions and manage responses efficiently. Keep the Start-Up Lead, Regulatory Lead, and Project Manager or Project Team informed with regular updates on submission status. Maintain project plans, trackers, and regulatory intelligence tools relevant to assigned responsibilities, ensuring Regulatory Leadership stays updated. Support the creation of study-specific start-up plans, define IMP release requirements, and set essential document review criteria. Work closely with the assigned site CRA to foster communication and site engagement throughout the study start-up process. Requirements Background in contracts and budgeting negotiation specific to the Spanish clinical research market. This position is remote and open to candidates based in Spain.

Join Eurofins Scientific as an Electric/Electronic Regulatory Affairs Technician in our Barcelona office. In this role, you will be at the forefront of ensuring compliance with regulatory standards for electrical and electronic products. Your expertise will contribute to the success of our innovative projects, allowing us to deliver safe and high-quality solutions to our clients.

Join Eurofins Scientific as a Temporary Chemicals Technician specializing in Regulatory Affairs. In this role, you will play a pivotal part in ensuring compliance with industry regulations for non-food and non-pharmaceutical products. You will collaborate with various teams to manage documentation, conduct testing, and maintain quality standards. If you are a detail-oriented professional with a passion for chemicals and regulatory compliance, we want to hear from you!

About the Role SGS is hiring a Regulatory Inspector focused on mechanical areas in Sant Joan Despí. This entry-level position supports safety and quality across multiple industries by checking compliance with relevant regulations and standards. Main Responsibilities Conduct inspections of mechanical systems and equipment Prepare clear, accurate reports documenting findings Work directly with clients to help them meet regulatory requirements What This Role Offers This is a chance to start a career in regulatory inspection, with hands-on experience ensuring industry standards are met. The work supports both client operations and broader public safety.

About Docplanner Group Docplanner Group connects 24 million patients with 280,000 doctors each month, operating in 13 countries through brands like ZnanyLekarz, Doctoralia, MioDottore, DoktorTakvimi, and jameda. The company builds healthcare marketplaces, SaaS tools, and AI solutions that help clinics, hospitals, and medical professionals focus on patient care by simplifying daily operations. Learn more about Docplanner's products at pro.doctoralia.es. Why Work Here? Real Impact: Contributions support healthcare professionals in their mission to help patients. Agile and Scalable: Join a team of over 3,000 employees who value flexibility and collaboration. Shape the Future: Play a role in the company's growth and long-term success. Role Overview: Senior Healthcare Regulatory Specialist (SaMD) This is a remote-friendly position based in Barcelona. The Senior Healthcare Regulatory Specialist will join the Risk & Compliance team, focusing on Software as a Medical Device (SaMD). The role supports Docplanner's expansion into medical device domains and ensures strict regulatory compliance as the company grows globally. The specialist will act as the Person Responsible for Regulatory Compliance (PRRC) under the EU Medical Device Regulation (MDR). Collaboration spans Product, Engineering, Machine Learning, Data, Customer Care, and Legal teams to ensure SaMD products meet regulatory requirements across Europe. The position is newly created and central to strengthening Docplanner’s regulatory framework, supporting EU MDR compliance and international growth. The role offers exposure to advanced health tech and AI-driven solutions, working with cross-functional teams in various markets. Key Responsibility EU MDR Compliance: Ensure Docplanner products achieve and maintain Medical Device Regulation certification for continued access to the European market.

Role overview Veeva Systems is looking for a Product Expert specializing in Regulatory Information Management (RIM) Submissions, with a focus on archive and publishing. This role supports clients in the life sciences sector, helping them manage regulatory submissions efficiently. The position is remote, with Barcelona, Spain as the listed location, but candidates across Europe are welcome. What you will do Use expertise in regulatory processes and submissions to assist clients in the life sciences industry. Guide clients through regulatory requirements and help them handle complex submission workflows. Contribute to the archive and publishing functions of Veeva’s RIM solutions, ensuring clients can organize and maintain their regulatory submissions effectively. Remote work This position is fully remote within Europe. Work from Barcelona or any other location in the region.

As a premier global transformation partner, Welocalize enhances business growth by helping brands and organizations connect with and expand their international audiences. We provide comprehensive multilingual content transformation services, including translation, localization, and adaptation across over 250 languages, supported by a network of more than 400,000 in-country linguistic resources. By merging technology with human expertise, we deliver innovative training data transformation solutions for NLP-driven machine learning, ensuring the highest quality in content collection, annotation, and evaluation. Our diverse team operates across North America, Europe, and Asia, serving clients in key global markets. Visit us at www.welocalize.com.As a Lead Recruiter specializing in Regulatory and Clinical recruitment, you will take ownership of the complete talent acquisition process within the CRO/Pharma sector, focusing on Clinical Trials, Pharmaceuticals, and Pharmacovigilance. You will lead a small team of recruiters and partner management professionals, balancing hands-on recruitment with team leadership and strategic execution of objectives.In this role, you will collaborate with cross-functional teams globally, tailoring your approach to align with the cultural expectations and communication styles of diverse regional teams. As an expert in Life Sciences recruitment, you will enhance candidate quality, ensure partner accountability, and provide data-driven insights to inform hiring decisions. Your proficiency with Lever will support effective pipeline management, targeted workflow automation, and precise reporting to leadership.

About Precision for Medicine Precision for Medicine is a global Clinical Research Organization focused on advancing precision medicine. The company blends innovative clinical trial designs with strong operational and medical expertise. Precision for Medicine specializes in rare diseases, oncology, and other therapeutic areas, and supports trials with advanced biomarker and data analytics solutions. Role Overview: Regulatory and Start-Up Specialist (Remote, Spain) This fully remote position is based in Spain. The Regulatory and Start-Up Specialist plays a key role in supporting clinical trial site activation and regulatory compliance. Experience negotiating contracts and budgeting within the Spanish market is essential. Main Responsibilities Ensure sites are ready for activation on schedule and to high quality standards, identifying and addressing risks early. Prepare Clinical Trial Application Forms and submission dossiers (including initial applications, amendments, and notifications) for Competent Authorities, Ethics Committees, and other local bodies. Follow local regulations and timelines to secure all required authorizations in line with ICH-GCP guidelines and company SOPs. Communicate with Competent Authorities and Ethics Committees to resolve study-related questions and manage responses. Provide regular updates on submission progress to the Start-Up Lead, Regulatory Lead, Project Manager, and Project Team. Maintain project plans, trackers, and regulatory intelligence tools relevant to assigned responsibilities. Keep Regulatory Leadership informed. Support the development of study-specific start-up plans, IMP release requirements, and essential document review criteria. Work closely with the assigned site Clinical Research Associate (CRA) to keep communication clear and aligned. Required Experience Proven background in contract negotiation and budgeting for clinical trials in Spain.

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.

Join our dynamic team at welocalize as a Lead Recruiter, specializing in Regulatory and Clinical roles within the CRO and Pharma sectors. You will play a pivotal role in shaping our talent acquisition strategies, ensuring we attract and engage top-tier candidates in these critical areas. Your expertise will be essential in navigating the complexities of the recruitment landscape, driving initiatives that enhance our hiring processes and elevate our employer brand.

About Ascendis Pharma Ascendis Pharma is a biopharmaceutical company focused on developing therapies for rare endocrinology and oncology conditions. With headquarters in Denmark and offices across Europe and the United States, the company’s work is guided by a commitment to patients, science, and passion. The proprietary TransCon® technology platform supports innovation to address unmet medical needs worldwide. Role Overview The Pharmaceutical Affairs Manager will oversee and advance pharmaceutical operations for Spain and Portugal. This position ensures compliance with Spanish, Portuguese, and EU regulatory standards, and supports quality management, pharmacovigilance, and regulatory interactions with local authorities. The role also involves assisting with quality and tender management. Collaboration is central to this position. The manager will work closely 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 role reports to the General Manager for Iberia. The position is based in Madrid, with a requirement to be in the office at least three days per week and flexibility for remote work on other days. Main Responsibilities Supervise regulated activities such as 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 the preparation and submission of local regulatory documents, including variations and notifications. Facilitate submission of materials for pre-approval to local authorities as required. Support administrative tasks related to regulatory documentation (such as Certificado de Exclusividad). Quality Management Assist with local implementation of the Ascendis Quality Management System. Serve as the QA/compliance contact for the local affiliate, working with the global QA team. ...