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.
The purpose of this position is to familiarize with relevant Quality Control methods, execute assigned products/materials’ analysis, and complete the required documentation according to established specifications and procedures.
Duties & Responsibilities
Performing the necessary tests for raw materials, and the products’ intermediate, final and under stability studies, according to written procedures and specifications. Proceeding with the completion of the required documentation.
Ensuring that all executed analysis follow the procedures of the analytical methods.
Checking the documentation and results of the analysis prepared by the QC Department, as and when requested to ensure the validity of the analysis and conformity with regulations.
Monitoring equipment maintenance needs, keeping the working area clean and tidy and promptly informing Laboratory Engineers of any equipment troubleshooting needed.
Reporting updates as regards the status of analysis to QC Supervisors and conducting relevant investigations when necessary.
Completing tasks and analysis in accordance with established regulations and guidelines such as Standard Operating Procedures (SOPs), current Good Laboratory Practices (cGLP), and current Good Manufacturing Practices (cGMP).
Carrying out any other duties as assigned by Supervisors
Requirements
Education: Bachelor’s degree in Chemistry, Chemical Engineering, or another relevant scientific field.
Non‑Regulated Training: On‑the‑job training provided on company processes, analytical methods, and regulatory requirements (SOPs, GMP, GLP).
Experience: Previous work experience is considered an advantage but is not a prerequisite.
Language knowledge: Good knowledge of Greek and English languages.
Digital Skills: Basic knowledge of Microsoft Office tools. Familiarity with laboratory software and ERP systems is an advantage.
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