Formulation Scientist - Topical and Oral Liquid

Role Overview: As an R&D Executive at PTC - CHANGODAR, your main responsibility will be the formulation development of topical dosage form and oral liquid dosage form for regulatory markets. Having additional experience in solid dosage form will be advantageous. You will be required to conduct literature search for assigned projects, plan and organize day-to-day research activities under the guidance of the group leader to ensure timely completion of projects. Additionally, you will be responsible for preparing various documents such as PDR, MFC, BMR, scale-up protocol, and other technology transfer and regulatory documents. You will also provide support in manufacturing clinical, scale-up, and exhibit batches whenever required. Key Responsibilities: - Formulation development of topical dosage form and oral liquid dosage form for regulatory markets - Conducting literature search for assigned projects - Planning and organizing day-to-day research activities for timely project completion - Preparation of various documents like PDR, MFC, BMR, scale-up protocol, and other technology transfer and regulatory documents - Supporting in manufacturing of clinical, scale-up, and exhibit batches when needed Qualifications Required: - Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or related field - Prior experience in formulation development of topical dosage form and oral liquid dosage form - Knowledge of regulatory requirements for pharmaceutical products - Strong organizational and time management skills - Excellent written and verbal communication skills (Note: No additional details of the company were provided in the job description.) Role Overview: As an R&D Executive at PTC - CHANGODAR, your main responsibility will be the formulation development of topical dosage form and oral liquid dosage form for regulatory markets. Having additional experience in solid dosage form will be advantageous. You will be required to conduct literature search for assigned projects, plan and organize day-to-day research activities under the guidance of the group leader to ensure timely completion of projects. Additionally, you will be responsible for preparing various documents such as PDR, MFC, BMR, scale-up protocol, and other technology transfer and regulatory documents. You will also provide support in manufacturing clinical, scale-up, and exhibit batches whenever required. Key Responsibilities: - Formulation development of topical dosage form and oral liquid dosage form for regulatory markets - Conducting literature search for assigned projects - Planning and organizing day-to-day research activities for timely project completion - Preparation of various documents like PDR, MFC, BMR, scale-up protocol, and other technology transfer and regulatory documents - Supporting in manufacturing of clinical, scale-up, and exhibit batches when needed Qualifications Required: - Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or related field - Prior experience in formulation development of topical dosage form and oral liquid dosage form - Knowledge of regulatory requirements for pharmaceutical products - Strong organizational and time management skills - Excellent written and verbal communication skills (Note: No additional details of the company were provided in the job description.)