Job description Posted 04 March 2019

Description

Will be part of a team responsible for microbial analysis of the process and materials associated with pharmaceutical manufacturing.

The position involves microbial analysis of raw materials, components, intermediates and final products as well as environmental monitoring of the site.

Will be responsible for the maintenance, culture, speciation and enumeration of microorganisms, and will also support the regulatory area, QA audits and inspections (MCA/FDA).

Preference for a graduate in microbiology, with experience in isolation and speciation techniques.

Good aseptic techniques are required.

GLP knowledge and an understanding of pathogenicity and ecology of microorganisms would be useful. Physical monitoring of areas Aseptic techniques Working to GMP


Additional information about the process

All profiles will be reviewed against the required skills and experience. Due to the high number of applications, we will only be able to respond to successful applicants in the first instance. We thank you for your interest and the time taken to apply.