Candidate must have an injectable background. Candidate must have knowledge of Software like Lab Solution, Chromeleon & Spectrum. Candidate must have knowledge of Instruments like UV, HPLC, FUR, GC, LPC, TOC, Polari meter, Refractometer.
As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file.
Candidates with laboratory experience in human cell culture, animal handling and prior knowledge of developing therapeutics for different infectious and non-communicable diseases will be preferred
Genome-wide evaluation of host genetic variations that associate with high risk for neonatal sepsis and sepsis related mortality. PhD in any branch Life Sciences from a recognized University. OR M.Sc or equivalent degree in any branch of Life Sciences from a recognized University
Successfully launch assigned brands in a specialty segment in line with brand strategy. Plan and consistently achieve patients on therapy, unit targets and value targets. B.Pharm / M.Pharm / M.Sc. candidates preferred.
Participate in function-specific sub teams and fulfill assigned project tasks and responsibilities under supervision -Uses professional concepts and company's policies and procedures to solve a wide range of difficult problems in imaginative and practical ways.
AstraZeneca contributes meaningfully to the UK beyond the provision of our medicines and the benefits they provide to the health of the nation. We commissioned a report in 2009 to measure our significant investment to the UK economy, which includes investment in jobs and wealth creation. Oxera, an independent economic consultancy provided the analysis for this report.
Post : Associate Director, Clinical Regulatory Writing