Master Degree in Pharmaceutical Sciences First-class with GPAT qualification Preferably in Pharmaceutics from a recognized University. developing nanoformulations, mammalian cell cultures, and in vivo experiments. Synthesis of Polymers, peptides Characterization of physicochemical Parameter, Determination of anticancer therapeutic effect in the in vitro assay systems, Validation of the in vitro results in the in vivo animal models of tumor-bearing mice model and infectious disease models
Masters degree in Natural or Agricultural sciences or Bachelors degree in Engineering and Technology from a recognized university or Doctoral Degree in Science, Engineering, Technology, Pharma, MD, MS from a recognized university or equivalent
Graduate in Science, relevant subjects from a Consolidated recognized university with 3 years of work experience from a recognized institution or master's degree in the relevant subject or Pharm.D Doctor of Pharmacy from a recognized institution.
PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.
Post : Senior Regulatory Affairs Associate (Labelling)
Completes basic job-related responsibilities, including time sheets, expense reports, maintenance of CVs, training compliance, project deliverable archiving, participation in internal initiatives, projects as requested by management
Vendor Management, Contract testing laboratories qualification, Qualification and management of contract vendors and external service providers, QMS and compliance.
The candidate should have a Masters degree MS, M.Pharm, M.Sc preferably in any stream of Pharmaceutical sciences preferably in pharmaceutics and pharmaceutical analysis. Candidate age should not exceed more than 28 years on the last date of the application.
Ph.D. or M.Sc./M. Pharm in Chemistry, Pharmaceutical Science, Analytical Science, or other relevant field; Provides leadership to scientists working in monograph and standards development and revision by established SOPs, business practices, and procedures.
MSc in Organic, Analytical Chemistry with 2 years research experience in analytical chemistry especially mass spectrometry, HPLC or other analytical tools Or B. Pharmacy in Pharmaceutical Analysis with 2 years research experience in analytical chemistry especially mass spectrometry, HPLC or other analytical tools
PhD in life sciences those who have submitted thesis experience of working in a lab or training in the skills required is mandatory. Should have an ability to absorb the published information, design experiments and sharp sense for high quality aspects in research.