Work Schedule Other Environmental Conditions Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc allowed Job Description Working shifts: 24/7 shift pattern Working environment : Good Manufacturing Practices (GMP) ; cleanroom environment Position Summary: The role provides daily operational support to the Process Coordinator. The technician will focus on manufacturing, filling, inspection, and packing pharmaceuticals (both sterile and non-sterile). They will follow Standard Operating Procedures (SOPs) and Batch Manufacturing Records (BMRs), ensuring compliance with cGMP (current Good Manufacturing Practices). What will you do? Responsibilities: Operation & Manufacturing : Set up and operate bulk formulation, filling, inspection, and packing lines, ensuring correct processes for both sterile and non-sterile products. Quality Control : Complete batch documentation accurately, perform in-process checks, and ensure compliance with SOPs to maintain high-quality standards. Equipment Maintenance : Perform equipment checks, cleaning (including CIP and SIP activities), and report any issues. Operational Support : Assist with project validation, new product introduction, SAP transactions, and work with quality systems for GMP changes. Leadership & Team Support : Monitor team progress, track downtime, ensure accurate batch records, and provide leadership in the absence of the Production Coordinator. GMP Responsibilities Ensure all processes (manufacturing, filling, inspection, and packing) comply with GMP. Support deviations and investigations and carry out good manufacturing practices. Maintain a tidy and compliant environment. EH&S (Environment, Health & Safety) Responsibilities Follow emergency procedures and ensure safe work systems are adhered to. Report accidents, near misses, and breaches of safety protocols. Who we are looking for: Minimum Requirements/Qualifications: Experience in a pharmaceutical or regulated environment (MHRA and FDA regulations). Knowledge of clean room operations and aseptic manufacturing. Strong English and Math skills; a scientific background is crucial (e.g., A-Levels). Previous supervisory experience or ability to develop individuals. Lean systems and continuous improvement experience (Green Belt preferred). Understanding of pharmaceutical systems with HMI involvement. Aseptic block license (if required).