Master, Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences, Doctoral Degree in Science, Engineering, Technology, Pharma, MD, MS from a recognized University or equivalent.

Master Degree in Chemistry from a Recognized University with minimum 55% Marks. Masters degree in Pharmaceutical from recognized University OR Equivalent with minimum 55% Marks.

Postgraduate degree in Public Health, Statistics, Epidemiology, Health Sciences, Environmental Sciences, Life Sciences, Population Sciences, Demography, Health Economics, HTA, M.Pharm Pharmacy Practice with 3 years of experience

M.Sc. in Biotechnology, Biochemistry, Zoology, Life Sciences OR M. Pharma in Pharmacology. Hands on experience on cell culture, animal handling, molecular techniques

Master Degree in Biotechnology, Biochemistry, Botany, Biological Sciences, Life Sciences from a recognized University or equivalent.

Bachelor, Master of Science in Biology, Biotechnology or relevant discipline. A candidate with experience in molecular biology, immunology techniques, and animal mice, goat handling is desirable. Candidates with experience working as technical staff in a research laboratory will be preferred.

Method transfer of Pharmaceuticals Products and Materials. Analysis of In-process, Finished products and Stability study samples. Sampling and testing of Raw Materials, Packaging Materials and Water samples.

You will be responsible for executing or assigning the execution of batch records and log books, filling in various applicable formats, including line clearance and sampling formats, along with batch records review sheets.

Candidate should be proficient in GLP. HPLC. GC. Instrumentation, Chemical Analysis, Raw Material Analysis, FG Analysis, UV, FTIR, In-Process Sample Analysis, and Stability Sample Analysis. 

Good analytical hand, well experienced in wet chemical analysis. Hands on experience of GC, HPLC, UV preferred. Aware of Good Manufacturing and Good Laboratory practices. Well versed with documentations related to a pharma laboratory.

Execution of batch process as per batch processing record in Granulation, Compression and Coating, Packing. Execution of equipment operation & cleaning activities as per SOP

Alembic Pharmaceuticals Limited announced that it has received final approval from the US Food & Drug Administration for its Abbreviated New Drug Application Diltiazem Hydrochloride Extended-Release Capsules USP, 120 mg, 180 mg, and 240 mg.

Investigating and translating genomic evidence for public health response to SARS-CoV-2; M.Pharma, ME, M.Tech with 3 years of research/teaching and design and development experience with at least one research paper in Science Citation indexed journal

PhD, MD, MPH, Doctor of Pharmacy or any other equivalent Degree with minimum two years of experience in research. A minimum of three SCOPUS indexed Q1 publications in peer-reviewed journals are viewed positively.

Development of Animal Feed Products from Eri Silkworm; Indian Institute of Technology Guwahati, the sixth member of the IIT fraternity, was established in 1994.

For the last six decades Central Government Health Scheme is providing comprehensive medical care to the Central Government employees and pensioners enrolled under the scheme. Interested retired officials who are eligible to the Pharmacist Homeopathy/ Pharmacist Ayurveda/ JHAA post may apply

PhD in Life Sciences, Chemical Biology, Cell Biology, Life Sciences, Biochemistry, or Neurobiology. Expertise in mammalian cell and tissue culture, sample preparation and data analysis skills for proteomics and genomics. Knowledge of glycobiology, glycoproteins, and glycoproteomics.

The BioDelivery Center is embedded in the Drug Delivery and Biophysics of Biopharmaceuticals group comprising four senior scientists, more than 10 junior researchers, as wells as several undergraduate and visiting students at Department of Pharmacy

M.Sc. / B.Pharma; review the latest pharmacopeial updates, supplements and amendments by evaluating the updates required in the available document to ensure the compliance with the current pharmacopoeia through consent with regulatory body