Sadman Sakib Bin Rashed Email and Phone Number

Performing production of recombinant proteins using single use bioreactor, such as the Wave™ system (upstream and downstream operations, media and buffer preparations, equipment and materials handling, production, and facility support). Documentation of activities according to QMS by recording events in BPRs, logbooks, stock cards. Identification and participate in deviation investigations, CAPA and change control activities. Protein purification by using ÄKTA™ systems & Protein analysis by using SDS-PAGE, Western blot, UV spectroscopy, etc.BioLamina is a Swedish biotechnology company with a global presence. It offers an expansive portfolio of defined human recombinant laminin proteins, Biolaminins, for a variety of applications, including reliable expansion of human pluripotent stem cells and differentiation and maintenance of different specialised cell types, such as hepatocytes, cardiomyocytes and neural cells. By providing the cells with their biologically relevant matrix proteins, the natural, cell-specific cell-matrix interaction can be mimicked, leading to improved cell functionality, robust culture systems and safe cells for therapy. BioLamina is the only company on the market to provide full-length and chemically defined laminin proteins and the technology has been scientifically validated in many high impact journals.

Research, analyzing, and developing formulations in the early manufacturing of solid dosage of cardiovascular and anti-diabetic drugs. Designing and development of preclinical and phase I/II formulations, encompassing both small molecules and new modalities such as mRNA and oligonucleotides. Working within a GMP (Good Manufacturing Practice), GLP environment and also contribute to the delivery of clinical results. Operating the timely manufacture of various cardiovascular and anti-diabetic pre-clinical formulations and finished drug products, operating with practical hands-on processes in GMP facilities, monitoring regulatory requirements, and supporting documentation activities. My experience in Cardiovascular (Renata) and Psychiatric (Eskayef) portfolios have equipped me with a comprehensive understanding of in-sourcing, out-sourcing, and technology transfer activities related to Active Pharmaceutical Ingredients, Formulation, Packaging & labeling. Additionally, I have been actively involved in teaching and providing training to assistant scientist, operators and others to ensure GMP and SHE standards.Looked after the Cardiovascular & Diabetic Portfolio at Renata Ltd .

Conducting research, analysing, developing formulations, supporting & working in Research & Development unit, Production unit with proper flow of knowledge regarding small molecular drugs. Working within a GMP (Good Manufacturing Practice), GLP environment and also contribute to the delivery of clinical results. Teaching & providing training to the Medical Service Officers about the therapeutic & pharmacological activity of locally available generic drugs. . Responsible with activities like in-sourcing, out-sourcing and technology transfer of Active Pharmaceutical Ingredients, Formulation, Packaging & labelling.