Senior GMP Technician - High Potency ADC/API Manufacturing

Piramal Pharma Limited; United Kingdom; Remote; GBP 42,000 - 56,000; Full time

Job summary

Piramal Pharma Limited is seeking a Senior Manufacturing Technician to supervise the manufacture of high potency ADC/APIs in support of launched products and clinical trials, ensuring compliance with approved procedures.

You will manage suite readiness, line clearance, inventory control, real-time GMP documentation, and maintain 5S and SHE standards; you will train less experienced colleagues and drive schedule adherence.

Responsibilities

• Supervise the manufacture defined cGMP procedures to deliver high potency ADC/API’s in support of launched products and clinical trial programme.
• Proactive approach to suite readiness, structured monitoring, line clearance, BOM /Stock levels, sample control and SAP inventory.
• Takes on a key role with the introduction of new products , liaising and communicating with relevant departments on highlighted issues
• Ensuring all team members are adequately trained and deliver training as and when required
• Effectively utilise and motivate manufacturing team to obtained the required schedule adherence
• Possess good verbal and written communication skills.
• Ensure that all GMP documentation is completed "real time" and accurately in aim of right first time.
• Maintain high SHE Standards, carrying out all work in accordance with appropriate SHE systems.
• Ensure that 5’s and housekeeping standards are adhered too, and suites are "audit" ready at all times.
• Raise any deviations and REW’s as required.
• Progress any investigations , CAPA’s to completion through "Trackwise" within the stated timeframe
• Leads continuous progress within the suites.
• Deputies for Shift Team in their absence.

Job description

Piramal Pharma Limited is seeking a Senior Manufacturing Technician to supervise the manufacture of high potency ADC/APIs in support of launched products and clinical trials, ensuring compliance with approved procedures.

You will manage suite readiness, line clearance, inventory control, real-time GMP documentation, and maintain 5S and SHE standards; you will train less experienced colleagues and drive schedule adherence.