 Responsible for developing suitable dosage forms related to HHP & AHP requirements Support in conducting Scale-up trials for commercial production and provide support to production department in trouble shooting Provide costing for new products and existing products for AHP and HHP requirements Co-ordinate bioavailability/pharmacokinetic studies Providing support for determining the compatibility of extracts in food forms Clarifying roles, responsibilities and performance of subordinates and facilitate smooth and safe functioning of department Ensure appropriate documentation related to all aspects of the department activities To coordinate with purchase for alternate vendor development Support in introducing the implementation of quality systems and policies for efficient functioning of the department

Preformulation studies, formulation development and stability studies of the developed formulations in lab scale batches in coordination with other departmentsHighly capable in developing formulations in dosage forms like Tablets (Conventional, Sustained release, Delayed release, Mouth dissolving tablets etc), Capsules, Oral liquids, Dry Suspension, Creams etc.,Having good exposure to drugs from class I, Class II and Class III (Biopharmaceutical classification system.Development of New products of various dosage forms of Domestic and ROW MarketsReview the stability data of the new products developedDocumentation of new product development as per QAPReview of operating documents and Master documentsTechnology transfer of developed formulationsFamiliar with various Pharmaceutical processes, equipment used- their design, operation, GMP aspects, trouble shooting, critical factors involved in scale up activities etc., Sourcing of Raw Materials, reference sample and other requirements related to R&D

 Preformulation studies, formulation development and stability studies of the developed formulations in lab scale batches in coordination with other departments Highly capable in developing formulations in different dosage forms like Tablets (Conventional, Sustained release, Delayed release, Mouth dissolving tablets etc), Capsules, Oral liquids, Dry Suspension, Semi solids (Creams, Ointments, Gel, Lotions) Having good exposure to drugs from class I, Class II and Class III (Biopharmaceutical classification system). Development of New products of various dosage forms of Domestic and ROW Markets Review the stability data of the new products developed Documentation of new product development as per QAP Review of operating documents and Master documents Technology transfer of developed formulations Familiar with various Pharmaceutical processes, equipment used- their design, operation, GMP aspects, trouble shooting, critical factors involved in scale up activities etc.,  Sourcing of Raw Materials, reference samples and other requirements related to R&D