Support feasibility evaluations with database and literature searches as well as data generation.
serve as project manager for assigned projects.
Establish contacts with CRO/CDMO’s for development of wide range of generic products.
Monitor and report progress of generic product development at CRO/CDMO.
Conduct dossier evaluation as pharmaceutical experts.
Frequent travelling to initiate and monitor collaborations with CRO/CDMO’s is required.
Other tasks assigned by supervisors.
Qualifications
Master's degree in Science or Business (MBS/MSc/M Pharm or equivalent) from a reputed College / University
7 to 10 years of experience in formulation and generic product development of small volume and large volume parenterals, including complex injectables. Experience in semisolid/solid dosage forms would be an added advantage.
Capability to take project manager role/ or should have basic knowledge with respect to project management.
Assisting, planning, coordinating with the CROs for developing the product as per the agreed timelines.
Evaluation and identification of CRO, monitoring their activities to ensure activities are undertaken as per the agreed timelines with CRO.
Providing technical and feasibility support to CRO on time-to-time basis.
Should have understanding of product development timelines, milestones and estimated budgets.
Task oriented with learning attitude and Teamwork skills.
Good English communication skills (both verbal & written).
