Promea Therapeutics is a Biotech, diagnostics and medical devices manufacturing company specialising in immunodiagnostics, molecular diagnostics, and large volume parenterals. We aim to make a significant difference to domestic and ROW healthcare markets through greater access to quality diagnostics as well as critical care parenterals.

We have a dedicated team of highly qualified R&amp;D who are in constant pursuit of precision, quality, and innovation.

Our state-of-the-art manufacturing facilities drive quality production of our kits and devices to satisfy the needs of our customers.

Responsibilities: To learn SOP’s in the facility of work and carry out the following activities as per Sr Executives instructions: <ol><li>Make sure the facility is clean and tidy.</li><li>Prepare stocks and buffers required for purification.</li><li>Carry out the sterilizations of vessels as per the BPR’s and SOP’s.</li><li>Carrying out purification, pegylation, refolding and filtration process.</li><li>Cleaning and carrying out tangential flow filtration process.</li><li>Cleaning of chromatography columns and executing the purification using chromatography column and system.</li><li>Recording the process details in BPR and log books online.</li><li>Coordinating and sampling at different stages of the process as per the batch processing record and transferring the samples to Quality control for analysis.</li><li>Observation of any deviations and discrepancies in the batch stages and report to the Sr Executive / assistant production manager.</li><li>Inform to superior if there is a spillage, breakage of laboratory ware, leakage of air / steam / water in the facility.</li><li>Inform the Sr. Executive / Asst. Manager incase of equipment malfunctions or breakdowns.</li><li>Actively participate in the internal and external audits and work towards the compliance to GMP’s.</li><li>Participate in the training programs conducted in the company.</li></ol>

Responsibilities:To follow SOP’s in the facility of work and carry out the following activities as per the SOP’s.<ol><li>Make sure the facility is clean and tidy.</li><li>Prepare stocks and buffers required for purification.</li><li>Carry out the sterilizations of vessels as per the BPR’s and SOP’s.</li><li>Carrying out purification, pegylation, refolding and filtration process.</li><li>Cleaning and carrying out tangential flow filtration process.</li><li>Cleaning of chromatography columns and executing the purification using chromatography column and system.</li><li>Recording the process details in BPR and log books online.</li><li>Coordinating and sampling at different stages of the process as per the batch processing record and transferring the samples to Quality control for analysis.</li><li>Observation of any deviations and discrepancies in the batch stages and report to the Sr Executive / assistant production manager.</li><li>Inform to superior if there is a spillage, breakage of laboratory ware, leakage of air / steam / water in the facility.</li><li>Inform the Sr. Executive / Asst. Manager incase of equipment malfunctions or breakdowns.</li><li>Actively participate in the internal and external audits and work towards the compliance to GMP’s.</li><li>Participate in the training programs conducted in the company.</li></ol>

Promea Therapeutics

Executive

Executive Trainee