Every pharmaceutical innovation, whether biotechnology, or pharmaceutical, starts out life within the Clinical Research stage.

Our client is a leading Clinical Research Organisation, at the forefront of the innovative life science industry, supporting hundreds of blue chip companies in getting their drugs to market and into the hands of patients that need these lifesaving drugs.

Due to securing new clients, and having a higher demand, our client is now looking for a QP to join their Quality Assurance team.

Role

As with all QP opportunities, the primary focus of this role surrounds batch release of products.  This company focussed on Clinical Research and IMP products primarily so may be a busy batch release environment although complexity will vary from batch to batch.

Alongside the core QP role, there will be elements of:

•              Supporting the QA team as part of the QA leadership

•              Providing Mentorship and Training to newer members of staff

•              Helping where needed in QMS workloads etc (however, mostly the other QA team will work on this)

There are also rooms for training and role development as the successful candidate gets into the role.

Requirements

• A Certified QP for Batch release
• Someone with experience of releasing IMPs as a QP or QP IMP (when that designation existed)
• Preferably someone with over 5 years Quality Assurance experience although a Newly Qualified QP would be considered even if they haven’t yet been on a license.

Remuneration

• £85K - £95K
• Strong benefits package including bonus

Respond

Click Apply now for more information, or contact Luke Blaney (Principal Consultant / Life Science Division) at our Falmer office.