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I am Busisiwe Madlala a biotechnology graduate with working experience in various fields such as beverages, pharmaceutical and a SANAS accredited water testing laboratory.
I am actively seeking employment.
National Diploma Biotechnology
I am a biotechnology graduate with working experience in various fields such as beverages, pharmaceutical and a SANAS accredited.
Work & Experience
Provide full admin support to the team and department. Perform data entry, documentation,printing and filing duties Maintain a proper and user friendly filing and document control systems Recording and tracking all documents Support the officers in daily admin roles and to keep stock of stationary supplies Put up purtchases requests for all approved purchases for the necessary approvals Verify invoices for the raised purchases upon delivery of goods and services Create and maintain useful databases for the department Responsible for receiving of all incoming specimen samples Capturing of data in the LIMS systems Responsible for sending out reports to clients once signed out by Phlebotomists/doctors Data capturing of excel input Create and prints fax sheets, memos ,mail,reports and other documents Schedule appointments maintaining and updating calendars,reminding respective personnel of the appointments Updating of master documents as per SOPs/Company policies.
Analyse all incoming raw and packaging materials for non-conformaties against company specifications and SOPs Maintain the quality management system for the area of responsibility to describe how the company complies with cGMP and operates to maintain a state of control. Keep abreast of changes to regulations and guidelines, advising the management team of any business implications of these changes. Assist in investigations with affected departments to establish the root cause(s) Assists in Training of Employees as required Review and updating of SOPs and WIs as required Assist in validation activities as required. Assist in laboratory quality assurance as required. Compiling and emailing weekly QMS tracker. Compiling and emailing monthly quality scorecard. Compiling information for APQR review for deviations and CAPAs. Compiling and emailing information for deviation and CAPAs for QMR. Manage the Deviation system to ensure the effective and timely implementation of non-conformances. Review and recommend improvements to the deviation system as and when identified. To ensure the organized collection and review of supplied supporting information to allow for proper evaluation of the proposed deviations. Liaise with Customer and other units (global) on an ongoing basis (e.g. changing of info on master docs, including tracking of documents couriered to them so that we do not experience delays in production). Close out of deviations. Trending and review of deviation logbooks. Follow up of outstanding information for deviations Generate and manage the collaboration of CAPAs with cross functional teams. Scanning and emailing all approved CAPAs to the respective teams and departments.