Gujarat

Deciphering the cellular heterogeneity in unstable atherosclerotic plaques using single cell RNA sequencing and spatial whole transcriptomics for developing RNA based prognostic markers; Candidates with prior research experience in human clinical samples, scRNA techniques are encouraged to apply. MSc in Biotechnology/Life Science

B.Pharm / M. Sc. Analytical Chemistry. Experience or Fresher Can also Apply; Preparation of Specifications in LIMS. Preparation of Methods in LIMS. Preparation of Standard Testing Procedures in LIMS.

GLP, Raw Material -Packaging Material, In Process-Finished Product, Method Verification Protocol preparation & Document Section Knowledge required; Water sampling/testing, EM Observation, Culture Handling, Media Management, Having Digital exposure for LIMS/ MODA Software B.Sc/ M.Sc/ B.Pharm; Lead QC operations as Shift In-Charge. Review analytical data, Ensure compliance with LIMS, GLP, ALCOA ICH/FDA

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

Responsible for designing overall marketing and communication strategy of brands; Good at Sales & Market data analysis; Must possess knowledge of product strategy, product launch. Torrent Pharmaceuticals announces hiring for a Product Management Team; B.Sc. /B.Pharma plus MBA

M.Pharm / M.Sc; HPLC/GC/IC method development, feasibility, verification, equivalency, validation for API, complex OSD products, oncology products, topical products having exposure to regulated, Semi Regulated and India markets; Good understanding and hands on experience of analytical instruments like HPLC, IC, GC etc.

Emcure is fast-growing Indian pharmaceutical company engaged in developing, manufacturing, and marketing a broad range of pharmaceutical products globally.

Experience in regulatory strategy, dossier review, and submission for the US, EU, and Brazil markets. This role requires a deep understanding of CMC requirements and the ability to lead the regulatory strategy for various dosage forms, including complex injectables and ophthalmic products.