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 assist in the execution of Quality Control tasks. Duties include processing and sampling materials, supporting analytical activities, performing physical tests, inspecting products and packaging materials, and accurately recording and maintaining quality data in accordance with approved procedures.

Duties and Responsibilities

• Testing identification of raw materials, intermediates, and bulk and packed products.
• Undertaking administrative duties, reporting, and filing using defined documentation and computerized systems.
• Performing sampling procedures for raw materials, intermediates, and bulk and packed products.
• Performing product physical control testing (such as weight, appearance, dimensions, disintegration, hardness, amongst others).
• Inspecting finished packed products to ensure they meet quality standards.
• Inspecting packaging materials to ensure compliance with quality standards.
• Handling stability samples, including receiving, storage, updating, and monitoring of relevant databases.
• Placing labels (Released, Quarantine, Rejected) on products and raw material containers.
• Collecting and storing samples in designated areas and registering them in databases or relevant electronic systems.
• Providing supplementary support activities related to the execution of analysis.
• Ensuring that bench work areas and laboratory equipment used are clean and properly maintained.
• Contributing to general laboratory housekeeping duties.
• Carrying out 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).

Qualifications and skills

• Previous work experience is considered an advantage but is not a prerequisite.
• Ability to work effectively within a laboratory team environment.
• Willingness to follow instructions and support team members.
• Ability to understand and follow written and verbal instructions.
• Accurate reporting and documentation of work performed.
• Ability to stand for extended periods.
• Ability to perform repetitive laboratory tasks.
• Accuracy and close attention to detail.
• Outstanding analytical abilities appropriate to the role.
• Good organizational skills and willingness to learn.
• Good knowledge of Greek and English languages.
• Ease with laboratory software, databases, and basic computerized systems.

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.