Job Purpose:The successful candidate will be responsible for ensuring adherence to the quality management system (QMS) and current Good Manufacturing Practices (GMP), as well as ISO 9001.Key Performance Areas:Product Release:• Authorising product releases and record verification.• Managing and controlling the process for the quarantine, sampling and release of product for sale.• Reviewing and releasing packaging material, raw materials, intermediate products and finished goods.• Inspecting retention samples as representative sample of batch.• Recommending product recalls where products do not meet specifications.• Controlling the issuing of labels and controlled printed materials (PIL, PI's, etc).• Serving as a member of the change control committee.QMS Principles:• Implementation of and guidance in QA GMP and ISO principles.• Making decisions according to approved GMP requirements, SOP's and/or corporate procedures and principles, within the scope of Deputy Responsible Pharmacist.• Ensuring compliance to GMP, with specific reference to radiopharmaceutical products - in-process inspections.• Preparing, updating, reviewing and approving procedures.• Updating QMS via structured procedures.• Training on GMP and relevant SOP's and related topics.• Maintaining and ensuring compliance to Quality agreements.• Preparing for and participating in Management Review.• Leading or partaking in risk assessments and validation activities, as appropriate.Product and Process Performance:• Coordinating and controlling stability program.• Performing Annual Product Reviews.• Performing Trend Analysis of various quality parameters for products.• Compiling monthly and quarterly reports.• Administering Continual Improvement System & leading or partaking in CAPA and/or Deviation investigations.• Establishing specifications.Audits and Projects:• Assisting in conducting supplier & internal audits and preparing for audits by third parties.• Reviewing new guidelines, outside inspection reports and current trends in GMP.• Assisting the Project Groups on various projects, in respect of QA activities on new product development and new facilities.Job Requirements:Knowledge and Skills:• Extensive knowledge of QA principles within the ISO and GMP environment.• Knowledge of ISO requirements.• Knowledge of GMP requirements.• GMP training.Competencies:• The ability to communicate effectively and efficiently at all levels in the organisation as well as in supplier organisations.• The ability to utilise the correct computer software and the relevant functionality applicable to the outcomes required.• The ability to manage time effectively and efficiently in accordance with work priorities to ensure qualitative outcomes.• The ability to apply planning techniques to conduct effective planning of work outputs and resources.Minimum Qualifications and Experience:• B.Pharm degree (NQF 8) or equivalent.• Registered as a practicing pharmacist with SAPC.• GMP training.• At least 5 years' experience in a pharmaceutical manufacturing environment of which at least 3 years are in a QA position.• Knowledge of ISO requirements.• Sound knowledge of GMP requirements.
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