Eugene Baxter Email & Phone Number

Epping/Stellenbosch

Extrinsic ControllerManage packaging Lab activities. • Ensure correct work instructions are used and adhered to.• Ensure that all equipment used is in good working order and calibrated where necessary.• Reporting and handling of non-conforming materials. • Communicate rejections to internal clients.• Ensure proper identification of suspect materials. Verification of master data for dry goods on system • Ensure that valid specs exist for dry materials.• Communicate all deviations regards material specs to QM&R • SAP Notifications• Monthly ReportKeep the Quality Manager informed of any non- conforming materials on incoming inspection and actions decided on.Assist with packaging related problem solving. Attend Supplier Meetings in the absence of the Quality Manager • Ensure instructions on lab tidiness and 5 S principles are maintained. • 5S audit results.Innovation and business improvements in support of operational and segment goals • Corrective action taken when deviations occur Risk, Health, and safety • Ensure compliance to OHSACT and all Distell Risk, Health and Safety procedures and statutory requirements.Health and Safety procedures and statutory requirements.Achieved business plan of Quality department • % Of initiatives successfully completed as agreed Quality management systems • Ensure compliance to the QMS (ISO 9001, ISO 14001, BRC, IFS, HACCP, Organic,ISO 17025, SANS 1841)• Ensure subordinates adheres to all relevant policies, procedures, work instruction andSOPs at all times• Initiate and motivate changes required to QMS system • QMS Audit findingsMaintain SANS 1841 certification for the site • Updating of documentation.• No of findings in internal and external audits.• Assist and evaluate product quality in the Trade Internal Audits • Compile & complete findings• QMS Audit findings

Epping

Stellenbosch, Western Cape, South Africa

Ensure at Plant level, in liaison with the Plant Manager that all quality related policies and procedures are adhere to.Drive improvement initiatives and process improvement projects. Drive Quality processes and ensure adherence of processes across the production siteFacilitate problem solving in Quality and the packaging environment. Manage suppliers according to the company's development strategy. Drive service level agreements between Quality and other departmentsBuild effective and trusting relationships with customers/suppliers to deliver on service level agreements. Drive and reduce write-off cost and implement improvement opportunities.Develop plans and review performance against targets regularly to ensure continuous improvements. Build trusting leadership development opportunities amongst all in the quality department.Provide targeted and regular feedback about company performance in line with organizational objectives. Ensure that the Quality team have clear, measurable goals.Develop & build talent management Manage projects within the Quality department as well as assist with projects in production.Form part of problem-solving teams and develop peers to deliver excellent problem-solving results. Create an environment for risk rating improvements and sharing of knowledge.Prepares monthly reports and quality documentation.Drive and enhance the quality site systems, 5's and lean methods. Make critical quality decisionsRoot cause analysis and implementation of corrective actions. Provide technical support in packaging and process improvement. Management of Non-conforming products and packaging.Management of consumer and customer complaints.Manage Supplier/Customer relationships.Facilitate Supplier performance meetings.

Administration-Logs packaging components and test data in LIMS.-Prints Certificates of Analysis, labels and various reports.Files COA’s, control envelopes, specifications and retention samples-Controls the destruction of retention samples and records as per Procedure.Controls the issue of quality status labels aproved’&’rejected’)Print daily and monthly packaging laboratory reports and LIMS-Issues Laboratory reports, copies of COA’s, etc. for rejected packaging Components containers.-Back-ups lot record data (from LIMS) onto diskettes.Testing and Lot Release-Statistically samples packaging components as per specifications.-Tests compliance of packaging components as per cumented-Specifications and Approved artwork.-Ensures that applicable SOPs are followed and required records are completed.-Records results as per GLP requirements.-Reviews results for accuracy and reports and anomalies to Packaging Laboratory Manager.-Performs ‘peer review’ of data as required by Packaging Laboratory-Completes supplier alert form for faulty packaging components.-Enter the packaging component status (i.e. release or reject) onto the BPCS systemGLP & QMS - Ensures cleanliness of working and surrounding area.-Ensures preparation and storage of reagents as per SOPs.-Ensures that chemicals and supplies are ordered timeously.-Ensures that SOPs in use are current and notifies the ManagerInhouse TrainingGMP, Documentation practises, business senseGLP, leading edgeOperational excellence 6’sOE Advocate trainingBusiness writing @ workPrimeserv.ReferencesMrs. Ruwayda Vlotman Packaging Lab Manager – GSK 021 507 6197Mr. Michael Brink Stores Controller -GSK 021 507 6174Rameez Abrahams Quality Controller -Distell 021 530 2353Hennie Botha Quality Control Manager -Distell 021 530 2372

Diploma In Stores Management, Packaging Technologist

Matric