Microbiology

Experience in Pharmaceutical Company in Parental, responsible for line clearance activity, responsible for in process checks, responsible for sampling. Finished product checking before release, management and execution of process validation & media fill simulation.

To carry out nanoparticle formulations and basic cell culture work related to the project. BPharm OR MPharm or equivalent degree with one publication in SCI Journal and should have at least one year research experience are eligible to apply. Candidates with National level examination qualifications such as NET-JRF/NET-LS/GATE or equivalent. 

Master Degree in Biotechnology, Biochemistry from a recognized university. Research / working experience in regulatory framework, and having the experience of handling small laboratory animals, etc. Analysis of Micro- Nanoplastics in food matrices; Micro and Nanoplastics as emerging food contaminants : Establishing validated methodologies and understanding the prevalence in different food matrices

The candidate will be responsible for performing a range of wet-lab based analyses, which include routine semen analysis, sperm DNA Fragmentation Index assessment, Y-chromosome microdeletion testing, RNA extraction, DNA extraction, protein extraction, PCR analysis, and ELISA assays. These tasks will be carried out as part of the broader study objectives, ensuring high standards of accuracy and consistency.

The Manager Drug Safety Content Analysis will manage and supervise project’s PV Operations/training staff on a day-to-day basis, guiding performance of PV Operations staff in ongoing projects in terms of training, quality of deliverables, compliance with the timelines and relevant trainings.

handle R&D projects independently in the areas of epidemiology, big data analytics, drug/ target/ biomarker discovery, preclinical and clinical evaluation of medical devices, IVDs, therapies, vaccines, field feasibility studies of the novel interventions, and experience/ exposure to regulatory aspects of health technologies, IP protection, Technology transfer. Health policy development and implementation. MD, MS or equivalent degree recognised by MCI, NMC OR MBBS or equivalent degree recognized by MCI, NMC, with MPH from a recognised university OR M.Sc or MBBS or equivalent degree, recognised by MCI, NMC, with Ph.D. from a recognised University.

Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article. Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments.

Exposure to aseptic process activities, aseptic techniques, aseptic filling and sealing activities, and media filling activities. Experience in operating autoclaves and terminal sterilizers. Preparation of autoclave loads, loading and unloading of autoclaves and sterilizers

The candidate will work in the areas of biocatalysis, enzyme engineering and applied microbiology. Biocatalytic Manufacturing of Industrially Important Enantiopure β-Amino Acids. Masters degree in Microbiology, Biochemistry, Biotechnology, Microbial Biotechnology, Industrial Biotechnology, Pharmaceutical BioTechnology, Biochemical Engineering.