Pharmaceutical Manufacturing Operator
CurrentI was responsible for preparing aseptically dispensed products while ensuring strict adherence to Good Manufacturing Practice (GMP). Working as part of a team under the guidance of an Operations Manager, I performed various tasks to support the production of parenteral nutrition, chemotherapy, and compounded intravenous additives (CIVAS) for adults, paediatrics, and neonates in both NHS and private hospital settings.Key responsibilities included: •Aseptic Preparation: Ensured the sterile preparation of products by measuring and mixing components using appropriate apparatus, following specific batch sheets and Standard Operating Procedures (SOPs). •Compliance with SOPs and GMP: Consistently maintained compliance with SOPs, ensuring all processes were carried out in line with regulatory standards and GMP guidelines, ensuring product safety and quality. •Disinfection Techniques: Employed rigorous disinfection techniques such as spraying, cleaning, and wiping down to maintain sterility in the aseptic unit, preventing contamination during production. •Preparation of Equipment and Supplies: Prepared equipment and supplies for use in the aseptic unit, ensuring all necessary materials were available and sterile before compounding. •Stock Management: Monitored and managed stock levels, ensured items were used within their expiry dates. •Documentation and Record Keeping: Completed all necessary documentation in accordance with company policies, ensuring accuracy and traceability of the manufacturing process. •Collaboration and Continuous Improvement: Actively contributed to team meetings and shared best practices, supporting the continuous improvement of production processes within the aseptic unit.Through this role, I gained significant experience in aseptic techniques, pharmaceutical manufacturing, and adherence to regulatory standards, while developing strong teamwork, problem-solving, and attention to detail skills.
