The Executive PMO will be primarily working in the domain of Launch Management and Life Cycle Management of commercial products for the US and other regulated generics markets such as EU, Canada etc. The primary responsibilities will be as follows:…
The Manager Portfolio will be responsible for evaluating, prioritizing, and managing the company’s pipeline of generic drug development projects intended for highly regulated markets (US, EU, UK, etc). This role requires strong analytical skills, market awareness, cross functional coordination, and…
Job Summary: Performs microbiological testing of raw materials, intermediate/finished products, and environmental bio burden. Independence, leadership, and technical skills are required to maintain a functional, current and GMP compliant microbiology laboratory. Responsible for continually evaluating the laboratory systems to ensure…
The Stability Coordinator will be responsible for overseeing and coordinating stability testing activities for pharmaceutical development, ensuring timely execution of stability pull and testing schedules in collaboration with Contract Manufacturing Organizations (CMOs) and Contract Testing Organizations (CTOs). This role involves…
Managing Project Management activities for both internal and client projects. Managing New Product Launch Activities for both internal and client projects. Work with clients, contract manufacturing sites and other partners for timely delivery of the projects. Implement project management tools…
Operation, Maintenace and troubleshooting of BFS machine Lead Technology Transfer activities from FRD to internal and external (CMO) manufacturing sites for sterile dosage forms. Drive CMO selection based on technical capabilities, capacity, regulatory compliance, and project feasibility. Plan and execute…
1) Analytical method validation 2) Analytical method transfer 3) Analytical method verification 4)Having instrument knowledge on HPLC, UPLC,GC Master of Science Master of pharmacy
Candidate shall be capable of handling Formulation development, documentation and Tech transfer of complex injectables like Microspheres & other injectables/Ophthalmic products. M.Pharm with 7+ years experience
Candidate shall be capable to handle Formulation development activities in lab & plant for sterile products like Injectables, Ophthalmics, lyo products, Inhalations etc.. M. Pharm with 2 to 4 years experience