capacity creation, and reduction of cycle time Quality by obtaining SAHPRA site compliance, QMS /Cipla from stores Ensure timeous receipt of batch manufacturing and batch packaging records Co-ordinate daily calculations in real time Assists in re-design of manufacturing methods Performs training of staff on SOPs, Generation and close out of deviations and change controls Conduct regular internal and external audits Review ensuring the ‘real time' completion of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR)
internal document relating to the testing and manufacture of Active Pharmaceutical Ingredients (APIs) Responding authority queries Ensuring that annual product quality reviews are compiled according to cGMP standards to the testing and manufacturing process Compilation and /or update of manufacturing and cleaning instructions experience in pharmaceutical, cGMP, or chemical manufacturing environment Proven technical documentation compilation
internal document relating to the testing and manufacture of Active Pharmaceutical Ingredients (APIs) Responding authority queries Ensuring that annual product quality reviews are compiled according to cGMP standards to the testing and manufacturing process Compilation and /or update of manufacturing and cleaning instructions experience in pharmaceutical, cGMP, or chemical manufacturing environment Proven technical documentation compilation
Job Outputs: Compilation and/ or update of manufacturing and cleaning instructions according to internal proposed changes Ensuring that annual product quality reviews are compiled according to cGMP standards company procedures relating to the testing and manufacturing process Compilation and update of documents experience in pharmaceutical, cGMP, or chemical manufacturing environment Proven technical documentation compilation
Job Outputs: Compilation and/ or update of manufacturing and cleaning instructions according to internal proposed changes Ensuring that annual product quality reviews are compiled according to cGMP standards company procedures relating to the testing and manufacturing process Compilation and update of documents experience in pharmaceutical, cGMP, or chemical manufacturing environment Proven technical documentation compilation
product quality complaints, adverse events and medical enquiries to the relevant person in quality assurance/
product quality complaints, adverse events and medical enquiries to the relevant person in quality assurance/
Purpose: A manufacturing company that specialises in reinforcement products is seeking a Intercompany
Purpose: A manufacturing company that specialises in reinforcement products is seeking a Intercompany
BBBEE compliance in line with targets set Cost Controls : Manage spend in line with budgets Identify cost