£55000 - £65000 per annum + benfits (negotiable)
26 Mar 2013
23 Apr 2013
Jade Tetlow
Full Time

Some general duties could include:

- To certify for release, batches of product manufactured by a third party in accordance with the Qualified Persons Code of Practice.

- Ensure aligned cell's KPI's, plans, targets and your personal/team objectives are effectively monitored and delivered.

- To carry out GMP audits.

- To approve for release or to reject starting materials, packaging materials, intermediate and bulk and packed products.

- Involvement in change control and deviation investigations.

- Manage completion of all documentation (GMP, statutory and regulatory) to the required standard and timescales, to ensure timely and efficient service for our internal and external clients.

You will need to be eligible for appointment as a Qualified Person under Directive 2001/83/EC with at least 5 years Pharmaceutical experience for all of these roles.

If you are interested in hearing more, please send an updated CV or call me on 0207 758 7311.

We also offer a candidate referral scheme where you will get £200 for each succesful candidate.

Keywords: GMP, GDP, batch release, manufacturing, quality assurance, QA, solid dose, sterile, aseptic, liquid, generics, CMO, third party

To find out more about Real please visit www.realstaffing.com