Quality Engineer - Pharmaceuticals

As the Quality Engineer within a pharmaceutical manufacturing environment you will be responsible for the following;
A focus on improvement activities for site processes,
Working with project teams for the introduction of new products & processes at the manufacturing site
Creation of technical documents & SOPs.
Significant involvement in process mapping and risk assessment activities
Investigation of site GMP issues

Proven experience and skills within the following areas is essential;
Minimum 2 years' experience in a pharmaceutical or Medical Device company in a technical or quality role.
A sound knowledge in GMP.
Experience or awareness of a range of ISO standards would be beneficial.
Previous experience of performing quality audits