Pune

Membrane preparation and characterization. Prior experience of working in research laboratory, industry desired. Direct Sea Water Electrolysis by electrolyte engineering & by coupling electrolyser directly with FO module.

research experience and knowledge in theoretical or computational biophysics, biophysical chemistry, protein dynamics, molecular dynamics simulations; Candidate should be familiar with enhanced sampling methods and MATLAB coding. Site-Specific Mechanism Of Aberrant Inter-Molecular Self-Assembly Of Full-Length TDP-43 In Neurodegeneration

Looking for clinical Database Developer experience in eCRF build and edit checks build in Veeva studio; Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process. Providing support for the mapping and transformation of clinical data to CDISC SDTM standards. Work independently and accountable for study Data Management deliverables; Coordinate with Biostatistician, Clinical, Medical and local study team as applicable

To achieve the sales objective for the Area of operation in order to meet the business targets for the area in a given time frame. To achieve the activity objective by ensuring the compliance to the field process in order to build an orientation towards activity process among the team.

After carefully observing all the instructions, the application should be submitted in the prescribed manner. Based on the information and documents provided in the application, the candidate's eligibility, ineligibility will be checked and based on that, he, she will be included in the further selection process. However, acceptance of the application or inclusion in the further selection process will not mean that the candidate is eligible for that contractual post.

B.Pharmacy from a recognized Institute. Or 10 plus 2 with Science stream Physics, Chemistry, Biology from a recognized Board. And Approved Diploma in Pharmacy from an Institute recognized by the Pharmacy Council of India and registered as Pharmacist under the Pharmacy Act 1948.

Oversee daily QC laboratory operations, ensuring compliance with cGMP, FDA, and other regulatory requirements. Validate, and implement analytical methods, including HPLC and plate-based assays as well as General assays. Ensure accurate and timely testing of raw materials, packaging materials, in-process samples, and finished products.

Conduct QC testing on raw materials, packaging, stability, in-process, and finished products. Capable of Handling Instrument like HPLC, GC,KF, IR,UV instrument. To review analytical data & handling of QMS i.e. Deviations, 00S, 00T, Laboratory incidences, OOC, CAPA and Effectiveness of CAPA.

Post Graduate Degree including the integrated PG degrees in Life Science Specialization required in Virology, Microbiology, Biotechnology, Biochemistry, Zoology.