Automated Tablet Inspection Operator

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Job Description

Automated Tablet Inspection Operator Part Time (FTC 12 Month)JOB OVERVIEW:

Based on an average working week of 18.375 hours, fixed term contract of 12 months.

Responsible for the operation of automated tablet inspection equipment, ensuring 100% inspection of manufactured tablet batches in accordance with approved procedures and GMP requirements.
The role involves managing the inspection process from receipt of product through to completion, including batch requests, equipment set-up, operation, in-process controls, defect categorisation, batch reconciliation and security tagging of finished product.
The successful candidate will be self-motivated, capable of working independently and confident operating computer-based automated systems. They will take ownership of their work, maintaining high standards of quality, housekeeping and GMP compliance whilst supporting departmental production schedules.

RELEVANT EXPERIENCE:

• Previous experience within a pharmaceutical manufacturing or GMP-regulated environment is preferred.
• Experience operating automated inspection or pharmaceutical manufacturing equipment would be beneficial.
• Confident using computer systems and automated equipment, with the ability to learn and navigate equipment operating software.
• Good attention to detail, particularly when identifying and categorising tablet defects.
• Ability to work independently, manage workload effectively and demonstrate a proactive, self-driven approach.
• Good organisational skills with the ability to prioritise activities and meet production requirements.
• Basic literacy, numeracy and computer skills required.
• Willingness to work within a 24/6 shift operation.

KEY ROLES/RESPONSIBILITIES:

• Operate automated tablet inspection equipment to ensure 100% inspection of manufactured tablet batches in accordance with approved procedures.
• Independently manage daily inspection activities, taking responsibility for the efficient progression of batches through the inspection process.
• Request and coordinate the movement of batches from the warehouse to ensure continuity of inspection operations.
• Responsible for equipment set-up, product changeovers and adjustments in accordance with standard operating procedures.
• Operate and navigate computer-based automated inspection systems, including the selection and adjustment of approved equipment settings within the scope of training.
• Monitor inspection equipment throughout batch processing, ensuring effective operation and minimising downtime.
• Perform and document all required in-process controls (IPCs) during inspection in accordance with batch manufacturing records and approved procedures.
• Following completion of inspection, review and categorise rejected tablets according to established defect classifications.
• Complete accurate batch reconciliations, accounting for inspected, accepted and rejected product in accordance with GMP requirements.
• Responsible for security tagging of inspected product in accordance with site procedures.
• Complete all relevant SAP transactions, batch manufacturing records and associated GMP documentation accurately and in a timely manner.
• Perform equipment cleaning, line clearance and routine operational checks in accordance with approved procedures.
• Identify and report equipment faults, inspection abnormalities and quality concerns, escalating issues appropriately.
• Carry out basic equipment troubleshooting and adjustments, within the scope of training, to minimise operational downtime.
• Take ownership of housekeeping and GMP standards within the inspection area, maintaining a clean, safe and organised working environment.
• Work proactively and independently, demonstrating good time management and the ability to maintain productivity with minimal supervision.
• Liaise with Warehouse, Production, Quality and Engineering teams as required to support efficient batch processing.
• Ensure all activities are performed in accordance with site safety requirements, GMP standards and established quality procedures.