Formulation R&D

As a Formulation Design & Development specialist, you will be responsible for: - Designing and developing robust, scalable formulations for oral solid dosage forms (OSDs) like tablets, capsules, and granules. - Selecting appropriate excipients, processing techniques (e.g., direct compression, wet/dry granulation), and equipment to meet target product profiles. - Conducting pre-formulation studies to evaluate properties such as solubility, hygroscopicity, flow, and compressibility. - Performing drug-excipient compatibility studies using thermal and analytical methods like DSC and FTIR. - Planning, executing, and supervising laboratory-scale, exhibit, and pilot batches while ensuring compliance with cGMP. - Optimizing manufacturing processes using tools such as QbD and DoE and evaluating scalability and reproducibility for commercial manufacturing. - Designing and initiating stability studies as per ICH guidelines and monitoring product behavior under different storage conditions. Qualifications required for this role include: - Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or related field. - Experience in formulation development for oral solid dosage forms. - Knowledge of cGMP guidelines and regulatory requirements. - Strong analytical and problem-solving skills. - Excellent communication and teamwork abilities. If you are looking for a challenging opportunity in a dynamic and innovative pharmaceutical company, this role might be the perfect fit for you. As a Formulation Design & Development specialist, you will be responsible for: - Designing and developing robust, scalable formulations for oral solid dosage forms (OSDs) like tablets, capsules, and granules. - Selecting appropriate excipients, processing techniques (e.g., direct compression, wet/dry granulation), and equipment to meet target product profiles. - Conducting pre-formulation studies to evaluate properties such as solubility, hygroscopicity, flow, and compressibility. - Performing drug-excipient compatibility studies using thermal and analytical methods like DSC and FTIR. - Planning, executing, and supervising laboratory-scale, exhibit, and pilot batches while ensuring compliance with cGMP. - Optimizing manufacturing processes using tools such as QbD and DoE and evaluating scalability and reproducibility for commercial manufacturing. - Designing and initiating stability studies as per ICH guidelines and monitoring product behavior under different storage conditions. Qualifications required for this role include: - Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or related field. - Experience in formulation development for oral solid dosage forms. - Knowledge of cGMP guidelines and regulatory requirements. - Strong analytical and problem-solving skills. - Excellent communication and teamwork abilities. If you are looking for a challenging opportunity in a dynamic and innovative pharmaceutical company, this role might be the perfect fit for you.