Join to apply for the Production Pharmacist role at Total Recruitment Solutions.Job Purpose: Providing best practice day-to-day manufacturing pharmaceutical services to manage workflow, production, and Document Procedure Compliance to ensure safe and efficacious medicines are manufactured. To comply with cGMP, MCC guidelines, SOP's, and adhere to batch documentation instructions at all times.Required LearningB. Pharm DegreeRegistration with South African Pharmacy Council2-3 years' experience in Pharmaceutical production in a manufacturing environmentcGMP skillsComputer Literacy – MS Office (proficient in Excel, Word, and PowerPoint)Key Job OutputsLead/champion changeovers, line openings, and line closings.Perform line opening checks and closures in manufacturing and packing lines.Review all production documents to ensure proper documentation of manufactured and packaged pharmaceutical products.Prepare weekly production scheduling of product.Ensure online and inline testing resulting in approval of batch documentation and provisional releases.In-process inspection performed as per SOP's.Correct material used per BOM.Non-conforming product has been handled and justification has been written where necessary.Product reconciliation.Submission of full production manufacturing tickets and supporting documentation within one hour of batch completions.Enforce Standard Operating Procedures.Update SOP's to ensure they reflect current practices.The correct SOP/ SPECS/PIC's /BOM were used during the production process.The correct measuring equipment was used and that the equipment was within calibration.Traceability of equipment and materials used has been maintained.The machines were set to the correct process parameters and that the process parameters used are validated.Ensure regulatory compliance with Safety, Health, and Environmental Standards.Develop the team's technical capabilities.Ensure that all production operators are trained for the tasks they are performing.Train operators on updated Standard Operating Procedures.Where necessary, draw up lesson plans and train as per the lesson plan.Lead and be the chief accountable officer for GMP and Micro compliance in the area on shift.Conduct monthly GMP audits, per SOP.Ensure that the working area and operators comply with GMP standards and SOP.Handling of non-conforming production, both inbound, WIP, and produced batches.Ensure the correct action has been taken to control non-conforming product, i.e., rework or discard.Investigate the cause of non-conforming product and ensure that adequate steps are taken to prevent re-occurrence.Ensure correct action instituted immediately.Ensure that if non-conforming products are corrected, it is subject to verification to ensure conformity.Write reports/justification to release the product where necessary.Auditing batch documents for QA closure and release.Assist in preparing Annual Product Quality Reviews.Prepare for audits and ensure compliance to standards.Initiate and close off CAPAs and Non-Conformances.Ensure corrective action is taken on all audit findings.Evaluate the effectiveness of the corrective action.Core CompetenciesAnalyticalNumericalAttention to detailMeticulousOrganizational AgilityExcellent verbal and written communication skillsAbility to plan and work independentlyDecision making and problem solvingAbility to adhere to required standards and objectivesAble to monitor and analyze own progress through available dataSeniority levelEntry levelEmployment typeFull-timeJob functionHealth Care ProviderIndustriesStaffing and Recruiting
#J-18808-Ljbffr
