PhD in Life Sciences and 2 years of experience in research and development in academic institutions or Science and Technology organisations. Masters Degree in Life Sciences, MVSC.
Ability to develop key partnerships internally and externally, influence and negotiate with key personnel, and plan strategically with a systems thinking approach.
Regulatory Affairs Manager prepare dossiers and execute actions that support the license security and product compliance on the markets, and that meet company's and health authorities’ requirements. Encounter the challenges to enable representatives from all major disciplines involved to reach agreement on the licence management strategy and approach.
Doctorate in Life Sciences or allied sciences from a recognized University with at least 10 years experience excluding the Ph.D. tenure, if any in at least 2-3 sectors including Industry, CRO, Technology Business Incubators, Start-ups, Innovation Management, or Academic, Research organizations.
Responsible to monitors activities at clinical study sites to assure adherence to Good Clinical Practices GCPs, Standard Operating Procedures, and study protocols under supervision of Clinical Operations Manager, Clinical Research Specialist.
Investigation on the Cohesive Roles of Glycogen Synthase Kinase 3 alpha and FTO in Regulation of Mammalian Spermatogenesis. M.Pharm., with first class and a minimum of 1 year of research experience after obtaining the highest degree.
Candidates having prior experience in plant-soil- microbial interactions, soil microbiology and microbiome analysis metagenomics, microbial screening, cultivation, characterization and enrichment studies, pathway/mechanisms analysis, microbial consortia development, state-of-the art molecular biology techniques, and detection of xenobiotics and secondary metabolites, LC-MS, GC- MS are encouraged to apply.
M.Sc, Microbiology, Biotechnology, Zoology, Botany from a recognized university or M.Sc. in life Sciences, Zoology, Botany, Marine Sciences, Chemistry, Environmental Sciences from a recognized university or equivalent.
Hands-on experience in DNA sequence data analysis from FASTQ files, particularly on Human genomic or Metagenomic samples using standard data analysis pipeline. M.Sc / M.Tech in Life Science or experience in bioinformatic analysis of genomic/meta genomic data or Ph.D.in Life Science