Trained on and support execution of DSP unit operations (chromatography, virus inactivation, virus filtration, ultrafiltration-diafiltration and drug substance final fill) with the applicable production protocols and planning schedules, in a clean room environment under cGMP conditions.
A pro-active attitude and personal initiative is encouraged to identify practical problems and communicates to the responsible person.
Contribute in their DSP functions, such as maintaining production suite, supplies, equipment, logbooks, and data, as well as closing out batch record and material reconciliation in accordance with site SOPs and policies.
Perform equipment maintenance and testing related to technical skills of Bioprocess Scientist DSP. Support and implement new procedures and/or equipment in the OPS department in consultation with other owners and users.
Revise and author SOPs and logbooks.
Adhere to Patheon cGMP Quality Management System and the Patheon EH&S requirements.
Complete corrective and preventive actions, contribute in deviation investigations and support the timely closure of deviation reports and change controls.
Implement lean (OE) initiatives and continuous improvements.
Contribute to the transfer and understanding of specific new technologies to DSP.
Connect with supplier about issued of technical nature.
Either experience in pharmaceutical industry OR tertiary education in science or engineering-based field (i.e. biopharmaceuticals manufacture, biotechnology, process technology).
Good understanding of cGMP practices.
Ability to work unsupervised. Good communication, flexibility, reliability and assertiveness. Responsible and proactive.
Qualifications
Either experience in pharmaceutical industry OR tertiary education in science or engineering-based field (i.e. biopharmaceuticals manufacture, biotechnology, process technology).
Good understanding of cGMP practices.
Ability to work unsupervised. Good communication, flexibility, reliability and assertiveness. Responsible and proactive.
