Remedica is a leading pharmaceutical company located in Cyprus with pharmaceutical products being distributed in more than 160+ countries worldwide. Originally founded in 1980, it went through various development stages. Today Remedica is specialising in the development, production, and sale of high-quality, safe, and efficacious pharmaceutical products for human use. Our pharmaceutical range consists of a product portfolio of more than 300 generic, branded generic, and over-the-counter (OTC).

Over the last few years, Remedica went through a massive transformational program from a locally recognized 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.

We are looking for:

A Junior Analyst to familiarize him/herself with relevant QC methods, execute the assigned products/materials’ analysis and complete the required documentation according to the relevant specifications.

 As a Junior QC Analyst you will be:

• 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/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 conduct the relevant investigation when necessary.

• Completing tasks and analysis in accordance with the established regulations and guidelines such as Standard Operating Procedures (SOPs), current Good Laboratory Practices (cGLP), and the current Good Manufacturing Practices (cGMP).

• Carrying out any other duties as assigned by Supervisors.

 What you will bring:

•  University degree in Chemistry, chemical engineers or any other relevant field. 

• Good communication and analytical skills.

• Good command of Microsoft Office

• Excellent command of the English language

• Previous work experience will be considered as 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.