Stelis Biopharma (A Strides Enterprise), We are a fully integrated pure-play biologics Contract Development and Manufacturing Organization (CDMO), offering the complete spectrum of services, from cell line technology transfer to clinical and commercial manufacturing with capabilities to convert drug substance into stable formulations and fill and finish formats. We have proven technical expertise in microbial, mammalian, viral vectors, and various other technology platforms with world-class cGMP manufacturing facilities that offer high-quality services for your global programs.
Stelis Biopharma -Walk in
- Qualification: Any Graduate
- Experience : 02-07+years
- Department: DP manufacturing
- Job Location: Bangalore Rural,Karnataka
Job description
01. Responsible for DP Manufacturing activities like compounding, Filtration, filling and Lyophilization of vial line products as well as cartridges.
02. Assist in Qualification and requalification of filling line Formulation vessels, Sterilizers Lyophilizer and isolators in Vial as well as Cartridge line.
03. Preparation and review of OQ, CLIA, QRM, BMR, SOPs and production related documents. 04. Ensure BMR, E-logbooks, protocols, QMS documents for compliance during manufacturing activities.
05. Interdepartmental coordination for the execution of the production batches as per the schedule.
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