Adcock Ingram is a leading South African pharmaceutical company with a proud 130 year heritage. It has a portfolio of trusted, quality brands and generics and an entrenched value system that assures integrity. Growing from humble beginnings as a small Krugersdorp pharmacy in 1890, Adcock’s portfolio includes an extensive range of Prescription, Over-the-co...
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Ensure that the production plan is updated as required
Translate targets into outputs
Ensure timeous availability of production materials
Ensures that the areas and equipment are clean and ready for use as per SOP
Ensure that documentation /materials are checked as per SOP
Ensure that sign off processes are done before declaration of areas
Authorisation of production documentation
Ensure yields are compliant
Initiate investigations for non-compliances
Audit documents post manufacturing
Perform transactions on Oracle
Prioritise action on arising shift problems
Report deviations to Pharmacist and Production Manager
Participate in internal and external quality audits
Participate in stock take
Monitor downtimes and drive problem solving and corrective actions
Ensure daily, weekly shift targets are met
Timekeeping of staff
Ensure training is completed as per plan
Improve and maintain machine availability
Improve productivity
Ensure change overs are done timeously (SMED)
GMP and regulatory compliance
Keep scrap/losses at a minimum
Ensure that safety standards are met
Provide a safe environment
Take necessary actions to manage production costs and improve profitability
Operate within and meet budget requirements
Maintains budgeted or better recovery to expense ratio
Lead cost saving projects
Provide an environment that promotes productivity, empowerment and learning
Ensure employees are empowered through MBU
Ensure and maintain high levels of performance as per output targets
Resolve IR issues
Requirements
Appropriate Degree or Diploma in Production Management/ Industrial Engineering, Operations Management and/or (Mechanical/ Electrical Engineering) or Equivalent
Preferably 3 - 5 years’ experience in a Manufacturing Environment
Knowledge of GMP/Pharma QMS
Computer Literacy – MS Office (proficient in Excel, Word and Power Point.