Content Management Specialist (Pharmaceuticals) - Tieto Tech Consulting (m/f/d)

Employment: Full-time Experience level: Mid-Senior Level Job Description Tieto Tech Consulting (MentorMate from 2001 to 2026) provides design-led, data-centric, and AI-powered digital engineering & consulting services to enterprises worldwide. With a strong heritage of Nordic quality, local presence, and global-scale operations, we are backed by 8,500+ IT professionals. Our clients trust us for advanced data and analytics skills, top industry-specific expertise, specialized software R&D, and the capabilities of a multinational team. We are part of Tieto, a leading technology company with an annual revenue of approximately EUR 2bn.     Tieto Tech Consulting’s team in Bulgaria consists of 500+ professionals specializing in the development of tailored digital solutions in diverse industries. We are looking for a Content Management Specialist to support the preparation, configuration, validation, and delivery of content for clinical studies. The role requires strong attention to detail, good coordination skills, and the ability to work with complex and frequently changing requirements. This role is based on a hybrid work model, with 3 days per week in our Sofia office. Key Responsibilities Manage study requirements and configuration files, including complex and frequently changing inputs Create, update, and manage different content types in Contentstack or other CMS platforms Coordinate content preparation, translations, testing, and deployment to production Validate content across different browsers, ideally using BrowserStack Work closely with different stakeholders and proactively request the information and inputs needed for delivery Work with pharma and clinical terminology and understand study-specific content and requirements Manage multiple priorities, detailed content changes, and tight delivery deadlines Ensure content is accurate, complete, and consistent before release Required Experience & Qualifications Very good communication skills and command in English Very strong attention to detail and comfortable working with complex or unstructured inputs Experience with CMS platforms and content operations Experience in pharma, clinical trials, or clinical study environments is a strong advantage Good coordination and communication skills Proactive approach to gathering information and following up with stakeholders Comfortable managing multiple priorities and working under tight deadlines Structured and reliable when handling detailed content and configuration changes A significant advantage would be Hands-on experience with Contentstack Experience with BrowserStack or similar cross-browser testing tools Previous experience working with clinical study content, terminology, or configuration Additional Information At Tieto, we believe in the power of diversity, equity, and inclusion. We encourage applicants of all backgrounds, genders (m/f/d), and walks of life to join our team, as we believe that this fosters an inspiring workplace and fuels innovation. Our commitment to openness, trust, and diversity is at the heart of our mission to create digital futures that benefit businesses, societies, and humanity. Diversity, equity and inclusion | Sustainability | Tieto Stay alert to recruitment scams: • Tieto only communicates via  @tieto.com  email addresses. • We never ask candidates to pay fees or share financial details during recruitment. • If you receive a suspicious message claiming to be from Tieto, don't respond — verify it via our official careers site. • For more information visit  Important Advisory Regarding Recruitment Fraud | Tieto Blog