Contribute to the development and implementation of new safety-related systems, processes, and procedures within the process.
Support a performance-driven culture.
Plan and coordinate with various departments like QA, QC and Production, to project the document requirements for appropriate submissions. Co-ordination with clients for the tracking and status update of project plans.
Master, Integrated Masters in Physics or Natural or Agricultural or Pharmaceutical Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University
Candidates having hands-on experience in Analysis of Raw Material, Packaging Material, Finished Goods, Stability, Method Transfer and Laboratory Investigations. Should have sound knowledge of QMS like Deviations, Change Control, Vendor Management etc.
To author and gain approval of scientific and regulatory submission documents that comply with global regulatory standards. To maintain key business relationships with appropriate cross-functional product team members.
Master, Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences, MVSc, Animal Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement
Masters in Natural or Agricultural or Pharmaceutical Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement; Establishing an IP search resource center at NCL
Monitor Global and Europe and Canadian markets for new product opportunities in both branded and Generic space In depth understanding of new product selection processes including portfolio management Primary responsibilities for executing out-licensing activities for the companies approved and In-development projects including financial modelling