Bangalore

Candidates with strong background in protein biochemistry, molecular biology and cell biology are encouraged to apply. Candidates are expected to have the ability to work independently, have good organizational skills, work in an interdisciplinary team, and manage multiple tasks. They will also be responsible for data documentation, validation and compilation, for preparation of manuscripts. Master degree in Life Sciences subjects or MVSc or Bachelors degree in engineering or technology

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

The educational qualifications remain the same as for the regular candidates. Qualifying in one of the national entrance tests like CSIR-UGC NET for JRF, UGC-NET for JRF, DBT JRF, ICMR JRF, GATE, and NBHM is desirable but not mandatory. Further, the candidate should have completed two years of full-time employment in the current organization after completion of degree. The candidates must be officially sponsored by their employing organizations and compulsorily fill in an online application form and submit the printed version, in duplicate, on or before 07th April 2025.

Good knowledge of triple quodrupole mass spectrometer platforms and demonstrated operational independence on these platforms. Experience in bioanalysis of small molecules is must to have and knowledge about other modalities such as biomarkers, cyclic peptides is preferred.

Drive science-based marketing strategies, focusing on PvP Product vs. Product, CvP Customer vs. Product, positioning, and differentiation to create unique brand identities. Graduation/Masters in Pharmacy / Biotechnology, with an MBA preferred. Take ownership of planning, implementing, and executing marketing activities in line with the brand’s calendar, brand plan, and Go-To-Market strategy.

Lab experience for Analytical Method Development, regular and stability sample analysis. Handling of HPLC for Assay, Dissolution, Related substances tests for solid orals. Perform pre-formulation studies, R and D trials and support scale-up activities Conduct R and D trials for oral solid dosage forms tablets, capsules, etc. M.Pharm / MSc

experience in drafting, filing and prosecution of Patent applications in India, coordinating with legal teams, advising clients on IP strategy and monitor compliance. Experience in performing comprehensive patent searches in curated database to identify relevant prior art and assess patentability.

Downstream and Upstream Manufacturing Mammalian and Microbial, QMS; DP Medical Device, Packing and Visual Inspection Labelling, Cartoning, Pick and Place Robotic Machines Handling and Track and Trace; DP and DS Engineering, Maintenance Automation, Instrumentation, Injectable Maintenance, QMS; M.Pharm, B.Pharm, MSc Chemistry, Biotechnology, Life science, Microbiology

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