Energy Jobline ZR
Formulation Scientist
Prana Biosciences is seeking a highly motivated formulation scientist to join the drug product formulation department. In this role, you will design and execute formulation experiments for innovative pharmaceutical development projects. Primary focus will be on developing tablet and capsule formulation using state of the art techniques. Demonstrate resourcefulness in running multiple activities related to solid oral dosage forms. The successful candidate will be expected to work effectively in a collaborative team environment. Responsibilities
This role offers a unique opportunity to contribute to the design and development of innovative drug formulations intended to follow the 505-B-2 regulatory pathway. Work closely with cross-functional teams to support formulation screening, preparation, and process development for novel formulations. Design and execute formulation studies for solid oral dosage forms. Prepare prototype formulations and conduct pre-formulation characterization (e.g., solubility, excipient stability, compatibility, flow property). Develop stable and bioavailable in-process materials such as amorphous pharmaceutical systems into solid oral dosage forms. Multi-tasks to effectively manage efforts on multiple activities and/or projects. Support analytical testing and interpretation of data related to physical and chemical stability. Prepare technical reports, presentations, and regulatory documentation. Stay current with scientific literature and industry trends in formulation and delivery. Qualifications/Skills
BS/MS degree in pharmaceutical sciences/pharmaceutics or related discipline. B.S. with 1-4 years or M.S. with 1-2 years of relevant experience. Familiar with tablet and capsule formulation techniques (wet granulation, dry granulation, direct compression) and stability studies. Familiar with Pre-formulation (solubility/compatibility/flow properties), excipient selection and compatibility studies. Familiar with FDA/ICH cGMP, GLP, CMC and Biopharmaceutics guidelines. Understanding of analytical test methods (Dissolution, disintegration, friability, hardness, weight variation, pH, moisture content, UV/IR and HPLC). 6 Preparation of batch manufacturing and formulation development records. Documentation as per GLP / cGMP standards.
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Prana Biosciences is seeking a highly motivated formulation scientist to join the drug product formulation department. In this role, you will design and execute formulation experiments for innovative pharmaceutical development projects. Primary focus will be on developing tablet and capsule formulation using state of the art techniques. Demonstrate resourcefulness in running multiple activities related to solid oral dosage forms. The successful candidate will be expected to work effectively in a collaborative team environment. Responsibilities
This role offers a unique opportunity to contribute to the design and development of innovative drug formulations intended to follow the 505-B-2 regulatory pathway. Work closely with cross-functional teams to support formulation screening, preparation, and process development for novel formulations. Design and execute formulation studies for solid oral dosage forms. Prepare prototype formulations and conduct pre-formulation characterization (e.g., solubility, excipient stability, compatibility, flow property). Develop stable and bioavailable in-process materials such as amorphous pharmaceutical systems into solid oral dosage forms. Multi-tasks to effectively manage efforts on multiple activities and/or projects. Support analytical testing and interpretation of data related to physical and chemical stability. Prepare technical reports, presentations, and regulatory documentation. Stay current with scientific literature and industry trends in formulation and delivery. Qualifications/Skills
BS/MS degree in pharmaceutical sciences/pharmaceutics or related discipline. B.S. with 1-4 years or M.S. with 1-2 years of relevant experience. Familiar with tablet and capsule formulation techniques (wet granulation, dry granulation, direct compression) and stability studies. Familiar with Pre-formulation (solubility/compatibility/flow properties), excipient selection and compatibility studies. Familiar with FDA/ICH cGMP, GLP, CMC and Biopharmaceutics guidelines. Understanding of analytical test methods (Dissolution, disintegration, friability, hardness, weight variation, pH, moisture content, UV/IR and HPLC). 6 Preparation of batch manufacturing and formulation development records. Documentation as per GLP / cGMP standards.
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