Job Description
Job Title:  Junior Formulation & Process Development Scientist
Job Location (Short):  Cyprus, Limassol
Req ID:  1032

Remedica is a leading pharmaceutical company located in Cyprus with pharmaceutical products being distributed in more than 140+ 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.

 

Job Description: 

 

We are looking for:

A Junior Formulation Scientist is to conduct Formulation and process development trials for new product development and re-development of existing generic drug products.

As a Junior Formulation & Process Development Scientist you will be responsible for:

  • Formulation 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.

 

What you will bring:

  • Bachelor’s in chemical engineering, Chemistry and Pharmacy
  • Master’s degree in pharmaceutical sciences preferred
  • 0-2 years of experience in relevant field
  • Very good spoken and written English required.
  • Ability to communicate in Greek is an advantage.
  • Proficiency in Windows, Word, Excel.
  • Prior knowledge of pharmaceutical research or manufacturing is an advantage but not an absolute requirement.

 

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.