Description
- 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).
Apply