Aseptic Clean Room Supervisor — Senior Assistant Tech

Cambridge University Hospitals NHS Foundation Trust; Cambridge; On-site; GBP 28,000 - 34,000; Full time

Benefits offered by this job

On-site leisure facilities

Day nurseries on-site

Subsidised parking

Job summary

Cambridge University Hospitals NHS Foundation Trust is seeking a Senior Assistant Technical Officer – Clean Room Supervisor to join the Pharmacy Sterile Production Unit in Cambridge. The role involves supervising aseptic preparation and dispensing, generating worksheets, and ensuring compliance with quality systems.

You will contribute to staff training and development while maintaining accurate documentation and audit trails for parenteral nutrition, cytotoxic medicines, and clinical trials.

Qualifications

• Experience of working in a sterile production unit within the NHS or Commercial Sector.
• Experience supervising aseptic preparation and dispensing activities.
• Ability to generate worksheets, labels and maintain documentation and audit trails.
• Ability to ensure correct use of equipment and adherence to SOPs.
• Willingness to contribute to staff training and development.

Responsibilities

• Assist the technician team with day-to-day supervision and coordination of aseptic preparation and dispensing in clean rooms.
• Generate worksheets and labels; assemble, prepare and dispense aseptic medicines for patients and clinics, including clinical trials.
• Manage recording and monitoring of clean room environments and equipment; report faults and deviations.
• Oversee in-process checking of measured dose units in parenteral nutrition and cytotoxic medicines; ensure product quality.
• Support development and implementation of new ways of working and updated policies.

Job description

Cambridge University Hospitals NHS Foundation Trust is seeking a Senior Assistant Technical Officer – Clean Room Supervisor to join the Pharmacy Sterile Production Unit in Cambridge. The role involves supervising aseptic preparation and dispensing, generating worksheets, and ensuring compliance with quality systems.

You will contribute to staff training and development while maintaining accurate documentation and audit trails for parenteral nutrition, cytotoxic medicines, and clinical trials.