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 R&D Operator supports formulation and process development activities through the execution of laboratory- and pilot-scale manufacturing and packaging operations, as well as equipment- and compliance-related activities.The role is responsible for equipment setup, material handling, batch execution, process documentation, cleaning activities, and the support of scale-up operations, in compliance with cGMP requirements, SOPs, safety standards, and data integrity principles.

Duties and Responsibilities:

• Execute formulation and process development batches, collect process data and report observations in accordance with approved protocols and batch records.
• Execute physical parameter testing for all materials.
• Prepare placebo batch records in accordance with instructions.
• Perform activities and operate laboratory- and pilot-scale equipment related to dispensing, blending, granulation, compression, encapsulation, coating and packaging.
• Set up, clean, assemble, and disassemble equipment.
• Maintain cleanliness and organization of laboratory and pilot plant areas.
• Conduct routine equipment checks and ensure calibration and maintenance status prior to use.
• Perform basic troubleshooting and support engineering team during qualification or repair activities.
• Complete GMP documentation, logbooks and batch records accurately and contemporaneously.
• Ensure compliance with SOPs, safety standards and data integrity principles at all times.

Qualifications and Skills:

• High school diploma or qualification at equivalent level
• Technical School Certificate in a mechanical field is preferred
• Some exposure to similar work (<1 year). Learning period: 3–6 months.
• Previous experience in a laboratory or production environment, or in a mechanical field involving sophisticated equipment, will be considered an advantage.
• Good communication skills
• Strong attention to detail 
• Good knowledge of Microsoft Office
• Excellent command of Greek and a basic level of English are required.

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.