Supervision of Micro Section Microbiological Analysis of Raw Material, Finished Product, Water Samples, Stability ad Hold Time study Samples. Review and Verification of Micro documents, Preparation of Protocols and SOP, QMS, Environment Monitoring Media Preparation, GPT Test, Microbial, Limit Test of Finished Product and Raw Material, Water Testing etc. - Calibration and Validation of Microbiological Instruments.

To Perform analytical activity of Development, Scale-up support, Method validation, Method transfer, Release, Stability, Drug product characterization, E&L study, In-Vitro study, routine analysis of inhalation dosage forms. M.Pharm, MSc

Diclofenac is having a cardiovascular health risk compared with non-use, paracetamol use, and use of other traditional non-steroidal anti-inflammatory drugs, as per research. The research was conducted by Morten Schmidt and published at the BMJ.

M.Pharma Medicinal Plant, M.Sc. Botany with specialization in taxonomy, Ayurvedic Medicinal Plants from recognized University, Institute. Project staff in the programme Management Unit of Regional Raw Drug Repository of Trans Ganga Plain Region RRDR at All India Institute of Ayurveda, Sarita Vihar, New Delhi, India. M.Sc Chemistry/ Analytical Chemistry/Medicinal Plants/Phytochemistry.

Ph.D. submitted in Microbiology, Plant Pathology, Agriculture, Life Science, Biological Science, equivalent. Plant Biochemistry, Microbiology Plant Microbe Interaction, Business Development, Agricultural Engineering, Bioprocessing, GIS & Remote Sensing, Knowledge Management, Fungus/ Mushroom, Material Chemistry , Crop Protection Plant Pathology

Knowledge in Computer Application. Eligible for training only if the date of commencement of training and the date of issue of last mark list of D.Pharm is less than three years.

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

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

Pyzchiva is a key biosimilar value driver for Sandoz, contributing to the company’s overall growth strategy. The company ranks number one in biosimilars globally and across key markets in Europe. The commercial availability of Pyzchiva, which builds on the US launch of Hyrimoz in July 2023, marks an important step in the Sandoz strategic ambition to become number one in biosimilars in the US.

Diploma in Pharmacy from any recognized Institution of the Central or a State Government for which the period of training in two years followed by an internship of which the practical training shall not be less than five hundred hours spread over a period of not less than three months, provided that not less than two hundred and fifty hours are devoted to actual dispensing of prescriptions

M. Pharmacy. B.Pharmacy from a recognized University, Institution. Preference will be given to the candidates possessing M.Pharmacy qualification.

Human Platelet Lysate Hydrogels As Therapy For Angiogenesis And Liver Regeneration. Preference will be given only to those with post graduate degree in Life Sciences, Biochemistry, Microbiology, Genetics, Pharmacology. Know-how and experience in Basic Animal handling and experimentation, Mammalian cell cultures, Molecular biology techniques.