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.

Job Purpose

The purpose of this position is to gain familiarity with relevant Quality Control procedures and analytical methods, perform assigned analyses of drug products and raw materials in accordance with established specifications and procedures, and complete all required documentation accurately and in a timely manner.

Duties and Responsibilities

• Perform the required tests and analyses of raw materials, in-process/intermediate products, finished products, and products under stability studies, in accordance with approved written procedures and specifications. 
• Complete all required documentation accurately and in a timely manner, in accordance with applicable procedures and Good Documentation Practices (GDP) 
• Ensure that all analyses performed are conducted in accordance with the approved procedures of the relevant analytical methods. 
• Review the documentation and analytical results prepared by the QC Department, as requested, to ensure the validity of the analyses and their compliance with applicable regulations. 
• Monitor equipment maintenance needs, maintain the laboratory work area in a clean and orderly condition, and promptly inform Laboratory Engineers of any equipment malfunctions or troubleshooting requirements. 
• Report updates on the status of analyses to QC Supervisors and conduct relevant investigations when necessary. 
• Perform all tasks and analyses in accordance with established regulations and guidelines, including Standard Operating Procedures (SOPs), current Good Laboratory Practices (cGLP), and current Good Manufacturing Practices (cGMP). 
• Perform any other duties as assigned by QC Supervisors. 

Qualifications and Skills

• Bachelor’s degree in Chemistry, Chemical Engineering, or another relevant scientific field. 
• Previous work experience is considered an advantage but is not a prerequisite. 
• HPLC hands on experience is preferred and considered an advantage
• Organized, cooperative, and adaptable to structured laboratory environments.  
• Ability to work effectively in 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 languages.
• Basic knowledge of Microsoft office tools
• Familiarity with laboratory software and ERP systems is an advantage. 

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.