Senior Training Scientist

Based in Limassol, Cyprus – comprehensive relocation support available OR hybrid options available for the right candidate (50% onsite in Limassol) Are you passionate about quality, compliance, and developing people in highly regulated pharmaceutical environments? Do you thrive on building training programs that drive both inspection readiness and operational excellence? At Remedica, we're looking for an experienced Senior Training Scientist, Quality Systems & Validation to take ownership of our GxP training framework and play a pivotal role in strengthening quality culture across our global pharmaceutical organisation. This is an exciting opportunity to become a key subject matter expert, shaping how training is delivered, governed, and measured across our business while working closely with Quality, HR, Manufacturing, and Operational teams. The Opportunity As our Senior Training Scientist, you will lead the design, implementation, and continuous improvement of our GxP training programme, ensuring employees across the organisation are trained, qualified, and inspection-ready. This is far more than a traditional training role. You'll drive strategic training governance, influence quality culture, and collaborate with stakeholders across the business to ensure training remains aligned with regulatory requirements, business needs, and industry best practices. Your work will directly contribute to maintaining the highest standards of compliance while enabling our teams to perform at their best. What You'll Be Doing Developing and maintaining a robust, compliant GxP training programme across key functional areasDesigning role-based training curricula and training matrices in partnership with Quality, HR, and operational leadersCreating effective onboarding pathways for new employees and GxP-relevant rolesEnsuring training programmes remain aligned with SOPs, regulatory requirements, and business processesDefining and measuring training effectiveness using risk-based methodologiesSupporting the creation and management of training materials, assessments, and qualification programmesMonitoring training compliance and driving actions to address gaps and risksLeading training-related activities arising from deviations, CAPAs, change controls, audits, and inspectionsSupporting internal and external audits and regulatory inspectionsDriving continuous improvement initiatives that enhance quality culture and inspection readiness throughout the organisation What We're Looking For You are a quality-focused professional who understands the critical role training plays in ensuring compliance, performance, and patient safety. You'll bring: A degree in Life Sciences, Pharmacy, Chemistry, Biotechnology, Engineering, or a related scientific disciplineAt least 4 years' experience within a GxP-regulated environment, such as pharmaceuticals, biotechnology, or medical devicesStrong knowledge of GxP requirements and Quality Management SystemsExperience translating regulatory expectations, SOPs, and operational processes into effective training programmesExcellent communication and stakeholder management skillsFluent Greek and English language skillsA proactive approach to problem-solving, continuous improvement, and compliance excellence Ready to Make an Impact? If you're eager to combine your GxP expertise, quality mindset, and passion for learning and development in a role where you can genuinely influence organisational excellence, we'd love to hear from you. Apply today and help shape the future of quality and compliance at Remedica. Remedica is a globally active EU-based pharmaceutical company, headquartered in Cyprus and present in more than 110 countries. Founded in 1980, the company has evolved into a trusted generics CDMO and dossier development partner for pharmaceutical companies worldwide. Remedica combines development expertise, EU-based manufacturing capabilities, regulatory know-how and a strong quality culture to deliver competitive, high-quality medicines. Its portfolio includes over 300 products across key therapeutic areas, including cardiovascular, oncology, anti-diabetic, anti-infective, central nervous system, alimentary tract, genito-urinary and musculoskeletal treatments. Over the last few years, Remedica went through a massive transformational program from a locally recognised reputable company to a global player, respected by its distributors, partners, and clients. The investments into the factories, R&D equipment, new facilities, implementation of best-in-class software, and people development are the baselines for Remedica's success in the future. Why Join Remedica? At Remedica, we offer a competitive compensation package, including 14 salaries, a provident fund, and a range of additional benefits to support your personal and professional growth. Join our team and be part of a company that values innovation, teamwork, and continuous improvement. Equal Opportunity Statement At Remedica, we are committed to ensuring equal pay for equal work and work of equal value. To support this commitment, roles are evaluated using a structured, gender‑neutral job evaluation framework, which objectively assesses the knowledge, skills, responsibilities, effort, and working conditions associated with each role. This approach helps ensure fair, transparent, and consistent outcomes across the organization.We welcome applications from all qualified candidates, regardless of sex, race, ethnicity, disability, religion or belief, sexual orientation, gender identity, or age.