Formulation & Process Development Scientist
Why REMEDICARemedica is a leading pharmaceutical company with a vision for a healthier world through high quality, safe and efficacious products at affordable prices.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..This role is based in Cyprus and requires relocationAs a Formulation & Process Development Scientist you will be responsible to:Evaluate product technical feasibility and strategic fit for development projectsIndependently 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 characterizationRisk assessments (e.g., DEC/FMEA)Prototype developmentProcess parameter definition and optimizationExecute 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 requirementPerform any other duties assigned by the Head of Formulation and Process Development for the product developmentWhat you will bring:Bachelor’s in chemical engineering, Chemistry and PharmacyMaster’s degree in pharmaceutical sciences preferred7-10 years of experience in a relevant fieldPrevious experience Oncology product development and experience in HME is preferableExcellent communication skillsProblem solving and Critical thinkingVery good spoken and written English required.Proficiency in Word, Excel D.O.E Software. Basic use of tools specific to the profession.What’s in it for you?13th and 14th salary.Provident Fund.Group Medical Plan.Discount scheme.If you are interested you can apply via our website: Formulation & Process Development Scientist Job Details | Remedica Limited