Job Description

• Ensure all training on equipment, processes, and facility and safety procedures are maintained and up to date at all times.
• Perform day-to-day manufacturing and cleaning activities to meet schedules while maintaining a high level of GMP compliance.
• To aid with troubleshooting and resolving operational problems during packaging.
• Ensure all documentation is completed to the required standard and within the specified timelines.
• Review batch records and other manufacturing process records as required.
• Routinely draft and revise standard operating procedures and master batch records.
• To aid in deviation investigations and closures.
• Support continuous improvement initiatives by identifying areas needing improvement, recommending strategies for improvement, and implementing those strategies once approved.
• Maintain a high, and continuously improving, level of GMP compliance to ensure patient safety and to minimize risk to the company business.
• Support Regulatory licensure activities, including agency inspections.
• Report to Area Supervisor on a regular basis on line performance and report any issues that need to be resolved.
• To train and be cross functional across all manufacturing areas of the packaging and warehouse facility.
• To perform any other task or duties as assigned by Area Supervisor.


•Third Level qualification in a scientific or engineering discipline or equivalent experience would be desirable.

• 2-5 years’ experience in Packaging Operations in a GMP environment.
• Must be able to work within and adapt to complex electronic systems such as SAP.
• Experience with warehouse equipment and systems preferred.
• Should be knowledgeable of regulatory and GMP requirements.