Responsibilities
The incumbent will be responsible for leading a team of scientists engaged in conducting formulation research and development activities on generic molecules, reformulation of existing drug products for life cycle management and new chemical entities. The area of formulation research includes solid and liquid dosage forms for oral, topical and parenteral administration to animals. The scope of research activities would typically include pre-formulation, prototype formulation and scale up studies as part of product development and subsequently the transfer of processes and technologies to commercial manufacturing sites. The position will involve developing and executing technical plans to meet target drug product profiles through in house research as well as external collaborations. The incumbent will be expected to ensure effective collaboration with various stake holders and customer groups such as global development team, regulatory, quality, manufacturing, marketing and clinical organizations for successful and timely delivery of clinical supplies and manufacturing process transfers. Other than the research activities the candidate will also be responsible for maintaining and delivering required documentation such as protocols, reports, SOPs, CMC technical sections for regulatory submission etc. Effective communication skills, leadership skills and people development skills are essential. The position would involve managing direct reports and travel up to about 25% of time.
Apply here
The incumbent will be responsible for leading a team of scientists engaged in conducting formulation research and development activities on generic molecules, reformulation of existing drug products for life cycle management and new chemical entities. The area of formulation research includes solid and liquid dosage forms for oral, topical and parenteral administration to animals. The scope of research activities would typically include pre-formulation, prototype formulation and scale up studies as part of product development and subsequently the transfer of processes and technologies to commercial manufacturing sites. The position will involve developing and executing technical plans to meet target drug product profiles through in house research as well as external collaborations. The incumbent will be expected to ensure effective collaboration with various stake holders and customer groups such as global development team, regulatory, quality, manufacturing, marketing and clinical organizations for successful and timely delivery of clinical supplies and manufacturing process transfers. Other than the research activities the candidate will also be responsible for maintaining and delivering required documentation such as protocols, reports, SOPs, CMC technical sections for regulatory submission etc. Effective communication skills, leadership skills and people development skills are essential. The position would involve managing direct reports and travel up to about 25% of time.
Apply here
Posts
