Job Description
Job Title:  Formulation & Process Development Scientist
Job Location (Short):  Cyprus, Limassol
Req ID:  1086

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 Formulation Scientist to be responsible for formulation and process development activities from early development through scale-up, validation, and technology transfer. The role requires a high level of technical expertise, independent decision-making, cross-functional leadership, and contribution to strategic R&D objectives, ensuring robust, scalable, and compliant pharmaceutical products..

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

  • Evaluate product technical feasibility and strategic fit for development projects
  • Independently conduct and/or oversee literature, patent, and regulatory research for RLDs, APIs, excipients, and manufacturing processes to support product development strategy.
  • Design, develop, and optimize formulations and manufacturing processes using Quality by Design (QbD) principles, including:
    • API and excipient characterization
    • Risk assessments (e.g., DEC/FMEA)
    • Prototype development
    • Process parameter definition and optimization
  • Execute feasibility, prototype, scale-up, and industrial-scale trials, ensuring processes are robust, reproducible, and commercially viable.
  • Execute formulation and process changes (including API changes) for both new and existing R&D-developed products, ensuring regulatory compliance and minimal impact on product performance.
  • Collaborate closely with Analytical Development, Stability Studies, Quality Assurance, Production, Regulatory Affairs, and Project Management to ensure aligned and timely project execution.
  • Provide scientific input for the preparation, review, and approval of stability protocols, reports, and shelf-life assessments.
  • Review and evaluate technical documentation and transferred-in formulations from external partners, ensuring robustness and successful integration into internal processes.
  • Perform in-depth analysis of scale-up and manufacturing data to identify trends, risks, and opportunities for continuous improvement.
  • Author and review high-quality technical documentation for development reports, technology transfer packages, regulatory submissions (CTDs), and responses to regulatory queries.
  • Ensure full compliance with SOPs, GDP, cGMP, and internal quality systems throughout all development activities.
  • Ensure strict adherence to health, safety, and environmental requirements, promoting a strong safety culture within the laboratory and production areas.
  • Prepare and review CRFs, technical justifications, and internal/external reports as required.
  • Evaluate latest amorphous solid dispersion technologies like Hot Melt Extrusion, Spray drying etc. as per product requirement
  • Perform any other duties assigned by the Head of Formulation and Process Development for the product development 

 

What you will bring:

  • Bachelor’s in chemical engineering, Chemistry and Pharmacy
  • Master’s degree in pharmaceutical sciences preferred
  • 7-10 years of experience in a relevant field
  • Previous experience Oncology product development and experience in HME is preferable
  • Excellent communication skills
  • Problem solving and Critical thinking
  • Very good spoken and written English required.
  • Proficiency in Word, Excel D.O.E Software. Basic use of tools specific to the profession.

 

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.