Quality Assurance Manager

• Jan 2023 - Present

Quality Assurance • Implement and champion an ISO QMS system, of an agreed upon best system e.g ISO9001 or ISO22000 •Liaise / ensure cooperation with all management to ensure harmonious and holistic implementation of a QA system • Amend/improve current QC systems to improve current workflows of all material stages from raw to finished • Implement any additional QC systems thought to be lacking • Analyze trends and improve product consistency and quality. • Create raw and FP specs • Liaise with management to create workflows, flowcharts around production lines • Create organogram • With managers, improve and optimize workflows to increase efficiency and reduce wastage • Curate retention production samples. • Oversee possible hygiene audits and/or any food audits (halaal/kosher/Food/GMP) (currently only have Halaal) • Ensuring legal obligations are followed and ensuring compliance with regulatory bodies and with health and safety guidelines • Gaining feedback from the clients, attending meetings, submitting reports, and assisting external auditors and inspector. QC • Carry out manual QC tests of all stages of material from raw materials coming in, intermediate / work in progress and finished goods. Training • Carry out staff training •Implement and carry out initiation training for all staff relating to the QMS and general company policy and procedures, e.g cleaning, behavioral, clocking etc…, as well as yearly refresher courses •Arrange for upskilling of staff and training relevant for specific requirements e.g ,health and safety, ISO courses •Train staff for new procedures implemented. Product development • Assist with concept and product development • Formalize a system for recording tests and results • Assist with interpreting results of tests • Assist in devising tests for product development and applications • Establish/formalize the process for product development from idea to final product approval Show less

Quality Assurance Specialist

• May 2022 - Dec 2022

Establish and Maintain the Quality Management Systems in relation to ISO9001:2015 by controlling external established and provided processes, products, and services to ensure they conform to requirements as follows: -Determining the controls be applied to externally provided processes, and products. Determining criteria for selecting suppliers. -Writing SOPs, and managing goods receiving inspection and warehouse processes. -Ensuring internal and external provided processes remain within the control of its quality management systems. - Assisting it in writing and compiling Supplier Agreements. -Managing the reused quarantine stock and offcut waste. -Report on monthly critical external providers and report on their performance in meetings. -Coach, mentor, and ensure the personal development of the team so that required expertise and skills are maintained. -Maintaining root cause analysis and corrective actions procedures. -Reporting To mansion a few. Show less

Quality Assurance Administrator

• Nov 2021 - Jun 2022

• Requesting and downloading release documents, ensuring that the correct documents have been furnished by the supplier. • Initiate, investigate, and close CC, CAPAs, and Deviations. • Conduct Product Trend Charts, Annual Product Quality Review, and Technical Quality Agreements. • Liaise with third party vendors to obtain the necessary qualification forms for new vendors and request updated documents for existing vendors when required. • To save and maintain all relevant documentation aligned to legislative requirements. • Receive products and initiate product release. • Log samples and Download data logger information. • Request order numbers for testing from Finance. • File release records (hardcopy and electronic). • Request sampling tracker if not sent by UPD on a weekly basis. • Complete checklist to ensure required docs for QA. • File reviewed data and completed report (hardcopy and electronic). • Request APQR when it is due. • Update the audit tracker and register once audit report is filed. Create lot release master documentation, when required. Show less

QC Chemical Stability Analyst

• Oct 2020 - Jan 2022

Is an area of great interest in preformulation studies. It is a complex set of procedures performed on candidate drug molecules or dosage forms that are in their final immediate packaging intended for marketing, and where appropriate, novel formulation excipients. By investigating the intrinsic stability of candidate drug molecules, useful information which is likely to improve the integrity of the drug products, as well as, prevent alteration in its physical properties, chemical properties and pharmacological effects are obtained. Preformulation stability analysis includes solid-state stability analysis, solution-state stability analysis and drug-excipients compatibility studies Show less

Medical Transcriptionist

• Aug 2019 - Jan 2020

health profession dealing with the process of transcribing voice-recorded medical reports that are dictated by physicians, nurses and other healthcare practitioners. health profession dealing with the process of transcribing voice-recorded medical reports that are dictated by physicians, nurses and other healthcare practitioners.

Classroom support assistant

• Apr 2019 - Nov 2019

CSS provides both reactive support - such as repairing faulty equipment - and proactive support, which helps to reduce technical faults that would otherwise delay lectures or hamper teaching time. CSS also maintains a pool of spare stock items so that audio-visual equipment can be quickly replaced or repaired as needed. CSS provides both reactive support - such as repairing faulty equipment - and proactive support, which helps to reduce technical faults that would otherwise delay lectures or hamper teaching time. CSS also maintains a pool of spare stock items so that audio-visual equipment can be quickly replaced or repaired as needed.

OTC Dispenser & Merchandiser

• Jul 2016 - Jan 2018