Job Description
Job Title:  Senior Formulation & Process Development Scientist
Job Location (Short):  Cyprus, Limassol
Req ID:  790

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.

 
Job Description: 


We are looking for:

A  Senior Formulation & Process Development Scientist to conduct research and formulation trials for product development and re-development of new and existing generic drug products

 

As a Senior Formulation & Process Development Scientist you will be:

  • Evaluating the product’s technical suitability at Remedica, especially for the critical and complex molecule/product

  • Conducting literature research on the originator drug product

  • (RLD)/drug substance prior to the initiation of lab activities

  • Designing of the formula & process as per QbD, evaluate equipment feasibility, API physical characterisation, DEC study, feasibility/prototype trials/scale up trials including the optimization of process and process parameters, stability testing in accordance to the specifications

  • Working closely with IP and reviewing patents and proposes non-infringing strategies for active pharmaceutical ingredients, compositions and manufacturing processes.

  • Planning, organising, follow-ups must be made to achieve target timelines among technical teams

  • Compiling/reviewing formal documentation required for product registration purposes

  • Ensuring that all performed tasks comply to the established regulations and guidelines such as Standard Operating Procedures (SOPs), Good Documentation Practices (cGDP) and the current 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

  • Minimum 7 years of previous Job experience in pharma sector

  • Attention to detail, accurate and precise in recording data and batch information

  • Strong analytical skills and mindset

  • Good leadership skills and timely decision making

  • Multi-tasking and ability to work under pressure with minimum supervision.

  • Excellent communication and organization skills

  • Fluency in English writing and speaking

  • Good MS skills (Word, PowerPoint, Excel)

 

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.
Apply now