Key Responsibilities:Lead and oversee multiple R&D projects, focusing on the development of innovative pharmaceutical formulations, including long-lasting injections and oral dosage forms.Closely interact and work with various cross functional teams like procurement, QC, QA, finance, manufacturing, regulatory affairs, to ensure that project is executed on time.Identify & co-ordinate with suppliers of raw materials, packaging materials, equipment, etc. and external agencies for analysis, preclinical & clinical studies to ensure that project is executed on time.To arrange scale up trials of various dosage forms developed.Preparation of high quality technical documents.To mentor and develop junior scientists and researchers, fostering their growth and enhancing their technical expertise.Foster a culture of innovation and continuous improvement within the R&D team.To collaborate with external partners, CROs, and academic institutions to enhance R&D capabilities and accelerate product development.To represent the Company in scientific conferences, industry forums, and customer meetings, showcasing R&D achievements and capabilities.To provide technical support to business development teams in identifying and evaluating new business opportunities.Candidate profile: Ph.D. / M Pharm in Pharmaceutics with 10+years of experience in formulation R&D.

Role & responsibilities 1. Shall have an exposure to SRA inspections like USFDA, EU, TGA etc.2. Should have experience of implementation and handling and troubleshooting any of QAMS software like Trackwise /calibre(DMS, QMS), nichleone(TMS), LIMS,SAP etc.3. Should have experience of handling QAMS notifications like change control, deviation, OOS, incidents, risk assessment, market complaint, etc.4. Should have an experience of MRM/ IPQA / participation in internal.Preferred candidate profile B. Pharm/M. Pharm with 4+yrs of experience in implementation of QAMS software, LIMS, SAP, nichleone.