Lead Pharmacists for Manufacturing and Accountable Pharmacist

• GPhC registration
• Aseptic experience
• Post-graduate qualification in clinical pharmacy/ aseptics
• Managing staff

• PTQA / equivalent
• Clinical Trials experience

Hi, my name is Michelle and I'm the Senior Pharmacist Manager for this team. I'm glad that you have looked at the vacancy and are thinking about if it is right for you at this time in your career. Are you a UK registered pharmacist with previous experience of aseptics or manufacturing? 
The role is an exciting one offering you the opportunity to focus on the aseptic dispensing of doses for patients in clinical trials or other novel agents. As the Accountable Pharmacist, you will be leading a dedicated team of pharmacists, pharmacy technicians, SMT and healthcare scientists who are passionate about research.  Can you show that you combine excellent technical knowledge and skills with those of positive people management?
The other aspects of the role is to support our manufacturing units for radiopharmaceuticals and hyperpolarised gas. Perhaps this isn't something you have done before; we can provide training.  
You will work alongside a knowledgeable QA team to ensure that GMP and QAAPS standards continue to be delivered. 
At last inspection CTAS was in March 2025 assessed as Low Risk by the SPS QA inspector and you will be in good hands.
We have strong team values and work together to deliver a timely and efficient service through kindness and support for one another.
If this role is of interest, then please get in touch for an informal chat and I look forward to potentially meeting you at interview. 

You will be the Accountable Pharmacist for the Clinical Trials Aseptic Services (CTAS) & responsible for the management, leadership and co-ordination of the unlicensed unit providing injectable Investigational Medicinal Products, Advanced Therapy Medicinal Products (ATMPs) and selected high risk injectable medicines to all trust divisions..
You will be responsible for the aseptic preparation of doses for a portfolio of c150 trials and ensuring that GCP requirements are met.
For the MHRA MS Radiopharmacy & Hyperpolarising Gas Units you will line manage the Production Manager(s) and ensure the service is run in compliance with current Good Manufacturing Practice (GMP). 
You will work closely with colleagues to ensure that clinical trials for IMPs are set-up  in accordance with sponsor requirements and align with UK,  trust and pharmacy best practices.
You will act as a role model and source of expert advice for pharmacy and clinical staff for aseptic preparation and ATMPs. 
You will act to ensure the safety of the patient and their experience remains at the centre of the service provided, while supporting the well-being of staff across the teams.
You will be supporting the building and commissioning of a new CTAS facility to further enable its extensive research portfolio.

Interview date - Wednesday 21 October - On site

You must have appropriate UK professional registration.

The postholder will have access to vulnerable people in the course of their normal duties and as such this post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service to check for any previous criminal convictions.