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. Deliver Precision. Support Excellence

Are you looking to build your career in Quality Control within a GMP-regulated pharmaceutical environment?

We are seeking a motivated Quality Control Analyst to join our team and support the testing and analysis of raw materials and pharmaceutical products, ensuring compliance with quality standards and regulatory requirements. The role will be based in Limassol, Cyprus.

In this role, you will perform laboratory analyses, review analytical data, maintain accurate documentation, and support the efficient operation of the Quality Control laboratory. You will play an important role in ensuring product quality, reliability of test results, and compliance with cGLP, cGMP, and company procedures.

Key Responsibilities

• Perform testing and analysis of raw materials, in-process/intermediate products, finished products, and stability samples in accordance with approved procedures and specifications.
• Complete laboratory documentation accurately and in a timely manner, ensuring compliance with Good Documentation Practices (GDP).
• Conduct analyses in accordance with approved analytical methods and established laboratory procedures.
• Review analytical data and documentation to verify accuracy, validity, and compliance with applicable requirements.
• Monitor laboratory equipment performance, maintain a clean and organized work area, and report equipment issues when required.
• Communicate analysis progress to QC Supervisors and participate in investigations as necessary.
• Ensure all activities are performed in accordance with SOPs, current Good Laboratory Practices (cGLP), and current Good Manufacturing Practices (cGMP).
• Perform any other duties assigned by QC Supervisors.

What We're Looking For

• Bachelor's Degree in Chemistry, Chemical Engineering, or another relevant scientific field.
• Previous laboratory or pharmaceutical industry experience will be considered an advantage but is not required.
• Hands-on experience with HPLC is considered an advantage.
• Organized, cooperative, and adaptable approach to working in a structured laboratory environment.
• Ability to work effectively within a team and follow instructions.
• Ability to work in a laboratory environment, including standing for extended periods and performing repetitive analytical tasks.
• Good knowledge of Greek and English.
• Basic knowledge of Microsoft Office applications.
• Familiarity with laboratory software and ERP systems will be considered an advantage.

Why Join Us?

This is an excellent opportunity to join a dynamic and quality-focused environment where you will gain valuable experience in pharmaceutical Quality Control. You will work alongside experienced professionals, develop your technical expertise, and contribute to ensuring the quality and safety of products that make a difference to patients worldwide.

Ready to Make an Impact?

Apply today and take the next step in your Quality Control career with Remedica!

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.