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.

Location: Limassol, Cyprus

Join Remedica and play a key role in maintaining and enhancing our Quality Management System, ensuring GMP compliance, operational excellence, and inspection readiness across our pharmaceutical manufacturing operations.

Key Responsibilities

• Lead and manage complex deviations, OOS investigations, complaints, CAPAs and Change Controls.
• Review and approve GMP documentation, quality records and quality system activities.
• Drive root cause investigations and risk assessments, ensuring effective corrective and preventive actions.
• Support GMP compliance, on-floor quality oversight and inspection readiness activities.
• Monitor quality metrics, trends and Product Quality Reviews (PQR/APQR).
• Collaborate with cross-functional teams to deliver continuous improvement initiatives.
• Mentor junior QA colleagues and provide quality guidance across the business.

What We're Looking For

• Bachelor's degree in Pharmacy, Chemistry, Biochemistry, Biology, Chemical Engineering or a related scientific discipline.
• 6+ years' Quality Assurance experience within a GMP-regulated pharmaceutical manufacturing environment.
• Strong working knowledge of EU GMP, WHO GMP, GDP and pharmaceutical quality systems.
• Proven experience managing investigations, CAPAs, deviations and Change Controls.
• Strong analytical, organisational and communication skills.
• Fluent English and Greek.

International candidates are welcome to apply. Relocation support is available for successful candidates moving to Cyprus.

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.