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.
Also, GLP knowledge and an understanding of pathogenicity and ecology of microorganisms would be useful.
Physical monitoring of areas, aseptic techniques, and working to GMP.
#J-18808-Ljbffr