Host-Diet-Gut Interaction Post Vegan Diet in Pediatric Autoimmune Hepatitis Project. Graduate in Life Sciences from a recognized university; AND Three years work experience from a recognized institution. OR Masters Degree in Life Sciences.

B.Pharmacy from recognized institute, Approved Diploma in Pharmacy recognized by the pharmacy council of India and registered as pharmacist under the Pharmacy act 1948.

Organize and dispense the drugs, medicines to the employees, pensioners. Maintain digital records of all the dispensary items, drugs. Any other work as assigned by the Competent Authority from time to time. experience as an apprentice trainee from a recognized Institution in Pharmacy trade

Lead optimization and in vivo proof-of-concept studies of novel alpha-ketoamide based protein aggregation modulators for Alzheimers disease. First class M.Pharm / M. S. Pharm. / M.Tech Pharm/ M.Tech in Medicinal Chemistry/Pharmaceutical Chemistry with GATE/ GPAT/ CSIR UGC-NET including lectureship or equivalent examination

Applications are invited from suitable candidates for the post of Research Associate to work on various NDDS level drug delivery systems for clinical applications in the IPCA foundation industrial project sanctioned to undersigned. M. Pharm, M.S. Pharmaceutics , Industrial Pharmacy or any other equivalent discipline.

B.Pharm with degree, diploma in Clinical Research Methodology. The candidate with a minimum 1 year experience in conducting clinical trial will be given preference. The candidate having experience in insurance sector will be preferred. TMC is an autonomous body funded, controlled by the Department of Atomic Energy, Government of India.

Exposure to OSD Manufacturing operations like Granulation, Compression, Pellet coaling, Capsule filling, Primary Packing & Secondary Packing. Expertise in e-BPR and e-log will he added advantage. Experience of HPLC, UV spectrophotometer and Dissolution Tester operation. Experience of Analytical Method Validation/Transfer. Experience of GC, ICPMS and/or LCMS operation.

Redaction of clinical trial documents in accordance with evolving global regulations. Develop training and drive change management for novel processes related to the EU Clinical Trial Regulation and other regulations. Manage and Coordinate redaction of clinical documents in accordance with EMA Policy 0070, Health Canada Public Release of Clinical Information, PRCI, EU Clinical Trial Regulation, and other global regulations. 

B.pharmacy and approved diploma in pharmacy. ECHS invites application to engage featuring medical, paramedical and non-medical staff on contractual bases in ECHS polyclinics ie Amritsar, Tarn Taran and Ajnala for a period of one year

Depyrogenation tunnel, Filling Machine, vial washing Machine, Autoclave operation, Aseptic practices etc. Shift handling, QMS, External vial washing, Sealing Machine, Filling machine, Aseptic practices

Support Analytical project leader for setting analytical development strategy. Support in data interpretation, results compilations and sharing the information with critical observations and proposals to project team.

Established in 1991, Lactose India Limited is a young and innovative company specializing in the manufacturing of Excipients Lactose, Colour Coatings, Lactulose, Solid Dosage Forms, Liquid Dosage Forms, at Vadodara, Gujarat.

B.Pharm or Diploma in Pharmacy from a recognized institution or board. Experience in dispensing and or storage and dispensing of drugs in a reputed hospital or institution or in a drug store or a pharmaceutical concern will be an asset.

Overall coordination and conduct of the project activities including analysis and report writing along with the study team. Candidate is required to coordinate with Institute, other Centers selected under this call for proposal and monitoring the work under of multicentric project and assist the Program officer in review of the data collected and preparation of reports and any other work assigned by Program Officer. 

Ph.D. with research in relevant area OR 1st class M.Tech or equivalent in Biotechnology, Food Technology, Dairy Technology OR 1st Class M. Pharma from a recognized University, Institute. Atleast 2 years analytical experience in the relevant field after essential qualification.

1st Class M.Sc, Masters degree in related discipline life sciences, Genetics, Biotechnology with 2 years research experience.

Syngene is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.

Hands on Experience for handling critical lab instruments like HPLC, GC, Dissolution, UV Spectrophotometer, LIMS, FTIR , experience in Analysis of RM, FP and IP stability in QC.

Candidate must have 2-7 years of experience in production, including operations and supervision of autoclave processes terminal sterilization and components, filter integrity testing, aseptic and controlled area operations, as well as proficiency in vial washing and filling machine operations.