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 conduct formulation and process development trials for the development of new products and the re‑development of existing generic pharmaceutical products, in accordance with established procedures and regulatory requirements

Duties & Responsibilites

• GFormulation and process development of new products including background research on planned new Remedica products and the carrying out of experiments in order to arrive at a stable formulation and a feasible manufacturing process
• Coordination and supervision of work at other companies for contract development of Remedica products
• Cooperate with Analytical Method Development and Validation for the assessment of prototype formulation performance. Based on this evaluation, planning of further formulation activities to ensure satisfactory development outcome
• Improvement of existing products in terms of stability, formulation and process
• Scale-up of R&D formulations into full-scale production
• Project management of technology transfers (to and from Remedica)
• Good Manufacturing Practices (cGMP).
• Carrying out any other duties as assigned by the immediate supervisor

Qualifications & Skills

• Education:  Bachelor’s degree in Chemical Engineering, Chemistry or Pharmacy; Master’s degree in pharmaceutical sciences preferred
• Experience: 0-2 years of experience in relevant field
• Interpersonal Skills: Ability to work both independently and as part of a team; Ability to work under supervision and collaborate across departments.
• Communication Skills: Good verbal and written communication skills
• Cognitive Skills: Attention to detail and ability to analyse data and support formulation decision‑making.
• Language knowledge: Good knowledge of Greek & English
• Digital Skills: Good knowledge of Microsoft office tools

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.