Discovery of Small Molecule based Cancer Immunotherapeutics and Vaccine Adjuvants. M.Pharm in Pharmacology, Pharmaceutical, Pharmaceutical Chemistry with 2 years research experience in Industry or Research Institutions or Universities.
Having experience in Injectable, Review of Calibrations, Preventive maintenance programmes. Review of utility systems and process equipment data. Review of alarms, Audit trails, drawings, investigations and Handling of Break downs.
Professional Science degree such as B.Pharma./B.Tech./M.Sc. Provide service support to the technical and scientific staff to ensure that all the specialized technology platforms are always kept in running conditions.
A Masters M.Pharm or M.Sc. or M.Tech. or M.E. or Bachelors B.Tech or B.E. or B.Pharm. An understanding of the Process Development and Industrial perspective of Biotherapeutics/ Biosimilars. Basic understanding of analytical techniques, statistical analysis, data management and analysis.
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.