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.
We are looking for:
A 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 Formulation & Process Development Scientist you will:
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Perform evaluation of the product technical suitability at Remedica.
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Conduct literature research on the originator drug product (RLD)/drug substance prior to the initiation of lab activities including Product & API patent (if applicable).
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Focus on technical aspects: 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 as per the guidance of Supervisor/Head.
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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.
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Cooperate with Technology Transfer and Scale up for the smooth transition of the prototype formulation to the production area.
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Cooperate with Project Management for verification of project status and establishment of department schedule.
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Do planning, organising, follow-ups must be made to achieve target timelines among technical teams as per the guidance from the Supervisor/Head
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Review of technical documents from external parties, undertaking communications with them, verifying the robustness of received formulations when transferred-in at small scale in the R&D unit. Preparation of summary reports to the Supervisor/Head.
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Proceed with Compiling/reviewing formal documentation required for product registration purposes.
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Provide scientific written responses, backed up with references to the applicable guidelines/literature, to deficiency letters from authorities.
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Maintain accurate records of the Formulation development activities.
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Be responsible for the proper application of personal protective equipment and safety procedures.
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Conduct preparation of the technical, non-technical reports (wherever applicable), product related documentation as per the SOPs & GDP.
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Prepare CRF’s when required.
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Ensure 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).
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Carry out any other duties as assigned by the immediate supervisor.
What you will bring:
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Bachelor in Chemical Engineering, Chemistry and Pharmacy
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Master’s degree in pharmaceutical sciences preferred
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Attention to Detail
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Strong analytical skills and mind set
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Demonstrated ability to work both independently and in team environments
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Excellent communication skills
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Good organization skills
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Ability to work under pressure
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Good command of English language and computer
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.