MAIN JOB PURPOSE:
To assist with the quality assurance service to the business so that products produced by the company are fit for use by the consumers according to Company’s specifications and standards.
To drive zero defect culture within the organization.
JOB SUMMARY
Operational
Carry out on line trouble shooting to identify product quality issues and generating of NCA in the event that quality defects are identified.
Carry out monthly checks discarding retention samples that are older than the specified retention period plus one-month.
Maintain an environment of 5s within retention storage area.
Participate in taste panels as approved tester and make decisions on status of products in terms of acceptance or rejection. (Mandatory that person does not smoke due to the negative effect this has on sensory evaluation which is a key component of the job)
Retrieval of samples from retention location and setting-up against Customer complaint sample and preparing all the necessary forms for evaluation.
Evaluating customer complaints against standards and completing evaluation documentation.
Prepare and write reports for consumer services team regarding investigated complaints.
Review of ex-factory CRQS data, entry onto SAP and trend and analyse reports.
Trending and analysing of CRQS EOLAS reports.
Lead problem solving kaizens derived from Q prioritization matrix to obtain zero defects.
Administrative
Daily filling of all reports/forms as listed below·
Retention Sample Register and generating of NCA's.
Weekly reporting consumer/customer complaints
Kaizen review and archiving of documentation to take place every two months.
Interact with QC technicians ensuring that information regarding non-conformance is logged and addressed.
Interact with production in the communications of quality problems identified in the packing process (during shift handovers)
Run all consumer and customer complaint investigations and generates reports for CEC feedback.
KEY REQUIREMENTS
Completed N.Dip or Degree in Microbiology/Biotechnology/Food Technology
Working Knowledge of HACCP and GMP's.
Working Knowledge of OHS act and safe operating procedures.
Ability to analyze data and information.
Please Attach:
ID copy
Qualification Certificate
Note: If you don’t hear from us within 14 days from the date that you applied, please regard your application as disqualified.
Unilever is an organisation committed to equity, inclusion and diversity to drive our business results and create a better future, every day, for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. At Unilever we are interested in every individual bringing their ‘Whole Self’ to work and this includes you! Thus if you require any support or access requirements, we encourage you to advise us at the time of your application so that we can support you through your recruitment journey.