February 2025

Bachelors Degree in life sciences with Full Time Post Graduate degree in Hospital or health care from a recognized university. At least 1 Year of experience in Hospital after acquisition of the aforementioned qualifications

Tracking Driver Mutations via sequential genomic profiling of Circulating Tumour Cells CTCs and Circulating Tumour DNA ctDNA in Cervical Cancer and their correlation with disease out come. Impact of elective para-aortic nodal radiotherapy on Human papillomavirus HPV circulating tumour DNA ctDNA kinetics in patients with cervical cancer: A nested biomarker discovery study in a RCT

Experience in polymer synthesis, polymer characterization, experience in animal experimentation, sample collection for serum analysis. Clinically relevant Three-Dimensional Bioprinted Liver Construct and its efficacy evaluation in Procine Liver Disease Model.

To monitor the Demo, Scale up, exhibit, and launch batches. To take scale up batch, Exhibit batches and work on Trouble shooting. To perform investigation for Deviation/ OOS/ OOT observed at plant.

Applications are invited for the temporary position of Junior Research Fellow for the Indian Council of Medical Research, Govt. of India sponsored project entitled, Cold Atmospheric Pressure Plasma for the treatment of chronic wounds – A Geroscience based approach under the Principal Investigator Dr. Kamatchi Sankaranarayanan, Physical Sciences Division, Institute of Advanced Study in Science and Technology, Guwahati, Assam.

This is a non-supervisory position in the Compendial Development Laboratory within Global Laboratory Operations. The incumbent will be responsible for performing analytical method development and validations for USP, NF monographs and maintaining safety and a GLP environment in the lab. Prepare and review project plans, reports, laboratory notebooks/Laboratory Management System LMS, and compile project data as required. Masters Degree in Chemistry Analytical/Organic or Pharmaceutical Sciences

Performing medical writing tasks for trial and/or non-trial activities within clinical reporting including but not limited to preparation of Protocols, Clinical Trial Reports CTRs, Non-interventional study reports NSRs, Layperson Summary LPS, Investigator Brochure and Regulatory response documents. PhD, MSc, MPharm, PharmD

Experience in IT, healthcare, or pharma; expert understanding of technology and methodologies as applied in the respective area. Good experience in technical planning, system integration, verification and validation, evaluating alternatives including cost, risk, supportability and analyses for systems total cost of ownership

Experience in injectable plant IPQA, GLP- QA, Tech Transfer, Validation, Qualification, QMS. Preference will be given to the candidates having experience of working in sterile pharma plant. M.Pharm, B.Pharm, M.Sc