Junior Pharmacist (Production) at Adcock Ingram

Responsibilities:

• Ensure all manufacturing processes comply with local and international pharmaceutical regulations.
• Conduct production line opening and line clearance checks as per SOPs.
• Monitor adherence to Standard Operating Procedures (SOPs) and Good Documentation Practices (GDP).
• Participate in regulatory audits and inspections, ensuring site readiness.
• Review batch manufacturing records (BMRs) and packaging records to verify compliance.
• Ensure correct SOPs, specifications, Bill of Materials (BOMs), and process parameters are followed.
• Verify calibration status of measuring equipment used during production.
• Check for proper traceability of raw materials, intermediates, and finished products.
• Handle batch-related deviations and non-conformances, providing justifications where necessary.
• Investigate non-conforming products, ensuring proper root cause analysis (RCA) is performed.
• Implement corrective and preventive actions (CAPAs) for product defects.
• Conduct trend analysis on defects and recommend improvements.
• Investigate and respond to customer complaints, ensuring issues are addressed promptly.
• Develop and update training materials and lesson plans for production staff.
• Train operators and supervisors on GMP, SOP compliance, and quality standards.
• Assess staff competency and ensure training records are maintained.
• Conduct monthly GMP audits and report findings to management.
• Update SOPs to reflect current production and quality assurance practices.
• Participate in internal and external audits, ensuring audit findings are addressed.
• Work on continuous improvement initiatives to enhance product quality and compliance.

Requirements

• Bachelor of Pharmacy (B. Pharm) degree from a recognized institution.
• Registered with the South African Pharmacy Council (SAPC) as a Qualified Pharmacist.
• Additional GMP, ISO 9001, or PIC/S certification would be an advantage.
• Strong knowledge of SAHPRA, GMP, PIC/S, and ISO 9001:2015 regulations.
• Ability to work shifts, weekends, and extended hours when required.
• Detail-oriented with strong analytical skills to evaluate production deviations.
• Proficient in Microsoft Office (Word, Excel, PowerPoint) and electronic documentation systems.
• Ability to work in a cleanroom environment and adhere to pharmaceutical hygiene protocols