Job description
TO supervise and coordinate daily activities within the Aseptic Unit,
acting as the lead point of contact for assigned areas and ensuring staff
activities, workflow, and operational tasks are effectively managed in line
with departmental requirements.
TO undertake the preparation and quality
checking of aseptic and non-sterile medicinal products, including chemotherapy
and parenteral nutrition, by following approved procedures, completing accurate
calculations, and maintaining required technical competencies within controlled
environments.
TO perform supervisory and accuracy checking
duties within Technical Services, including monitoring production processes,
reviewing documentation, supporting Good Manufacturing Practice (GMP)
standards, and ensuring deviations or quality concerns are appropriately
escalated.
TO support the maintenance of safe
pharmaceutical production environments by coordinating cleaning schedules,
monitoring facility standards, ensuring compliance with environmental
requirements, and promoting safe handling practices for hazardous substances.
TO manage stock control activities within
Technical Services by maintaining accurate records, completing stock checks,
investigating discrepancies, supporting procurement processes, and assisting
with the management of specialist and outsourced products.
TO contribute to team development and service improvement by mentoring
colleagues, supporting staff training activities, maintaining professional
knowledge through continued development, and identifying opportunities to
improve technical processes and working practices.
Job description
Job responsibilities
TO supervise and coordinate daily activities within the Aseptic Unit,
acting as the lead point of contact for assigned areas and ensuring staff
activities, workflow, and operational tasks are effectively managed in line
with departmental requirements.
TO undertake the preparation and quality
checking of aseptic and non-sterile medicinal products, including chemotherapy
and parenteral nutrition, by following approved procedures, completing accurate
calculations, and maintaining required technical competencies within controlled
environments.
TO perform supervisory and accuracy checking
duties within Technical Services, including monitoring production processes,
reviewing documentation, supporting Good Manufacturing Practice (GMP)
standards, and ensuring deviations or quality concerns are appropriately
escalated.
TO support the maintenance of safe
pharmaceutical production environments by coordinating cleaning schedules,
monitoring facility standards, ensuring compliance with environmental
requirements, and promoting safe handling practices for hazardous substances.
TO manage stock control activities within
Technical Services by maintaining accurate records, completing stock checks,
investigating discrepancies, supporting procurement processes, and assisting
with the management of specialist and outsourced products.
TO contribute to team development and service improvement by mentoring
colleagues, supporting staff training activities, maintaining professional
knowledge through continued development, and identifying opportunities to
improve technical processes and working practices.