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.

Drive Quality. Ensure Compliance. Support Excellence.

Are you passionate about quality, compliance, and continuous improvement within a GMP-regulated environment? We are seeking a dedicated Quality Compliance Scientist to join our team and help maintain and enhance our Quality Management System (QMS), ensuring the highest standards of quality, safety, and regulatory compliance. The role will be based in Limassol, Cyprus.

In this critical role, you will support quality assurance activities across regulatory compliance, audits, supplier management, quality systems, risk management, and inspection readiness. You will play a key role in ensuring compliance with current Good Manufacturing Practices (cGMP), regulatory requirements, and company procedures while contributing to the continuous improvement of our Quality Management System.

Key Responsibilities

• Serve as the primary contact for regulatory authorities and support Health Authority inspections.
• Ensure compliance with GMP requirements and global regulatory guidelines, including EMA and ICH standards.
• Maintain and improve the Quality Management System (QMS) through effective management of GMP documentation, Change Controls, CAPAs, and compliance processes.
• Monitor regulatory updates and implement required changes to quality systems and procedures.
• Plan, participate in, and support internal, supplier, and external audits, ensuring timely closure of audit actions.
• Manage supplier qualification activities, including onboarding, ongoing evaluation, and Quality Technical Agreements.
• Support the investigation and resolution of customer, supplier, and third-party quality complaints.
• Coordinate product recall activities, including mock recalls and related documentation.
• Monitor Quality Metrics, KPIs, and Quality Risk Management activities to support continuous improvement.
• Review qualification and validation documentation for equipment, processes, cleaning, computerized systems, and transport activities.
• Deliver GMP and compliance training and contribute to ongoing inspection readiness initiatives.
• Ensure all activities are performed in accordance with SOPs, GDP, cGMP requirements, and other applicable regulations.
• Carry out any other duties as assigned by the immediate supervisor.

What We're Looking For

• Bachelor's Degree in Pharmacy, Chemistry, Biochemistry, Biology, Chemical Engineering, or another related scientific field.
• 2-3 years of experience in Quality Assurance, Quality Control, or GMP-regulated pharmaceutical manufacturing.
• Ability to collaborate effectively with internal departments, suppliers, customers, and external stakeholders.
• Strong teamwork skills with a proactive, adaptable approach and the ability to perform effectively in a fast-paced environment.
• Excellent verbal and written communication skills, with the ability to communicate compliance and quality-related information clearly and accurately.
• Strong attention to detail and commitment to Good Documentation Practices (GDP).
• Excellent analytical, investigative, critical thinking, and problem-solving skills.
• Good understanding of GMP requirements (EU and WHO), GDP principles, pharmaceutical quality systems, and regulatory compliance requirements.
• Ability to assess risks, evaluate documentation, identify compliance gaps, and implement appropriate quality actions.
• Comfortable working in an office-based environment with extensive use of computer systems and quality documentation.
• Excellent knowledge of English Greek will be considered an advantage.
• Good knowledge of Microsoft Office applications.

Why Join Us?

This is an excellent opportunity to become part of a quality-driven and dynamic environment where your contribution directly impacts regulatory compliance, operational excellence, and product quality. You will work alongside experienced professionals, contribute to continuous improvement initiatives, and play an important role in maintaining the highest standards of quality and compliance across the organization.

Ready to Make an Impact?

Apply today and help us drive quality, ensure compliance, and support excellence across our operations as a Quality Compliance Scientist!

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.