We have an opportunity for QA Manager to take on a 6 months contract to manage projects and allocated resources according to required standards and timescales.
Review and recommend disposition of deliverables (e.g. procedures, records,
third party work, contractors, clinical trial material, components) and related
tools (e.g. IT, document systems, training tools, facility validation) to ensure
GMP compliance. Support project related activities (e.g. interpret results, evaluate data, draw
Perform inspections and audits as required
Contribute to the evaluation of new QA tools.
Write GMP relevant documents in own area of responsibility (e.g, SOPs with
Meet internal and external guidelines regarding quality and safety (quality
manuals, regulatory cGMP guidelines, health authority guidance, SOPs, HSE,
Promote and enforce compliance to guidelines
Education BS/MS or equivalent in scientific or relevant discipline Desirable: Advanced degree in scientific or relevant discipline (MS or equivalent)
Languages: Good knowledge in English (oral and written) required;
Relevant experience in the Quality assurance area Very good knowledge of cGMPs, working knowledge of safety and environmental regulations and guidelines.
Good knowledge of drug development .
Good ability to analyze and evaluate GMP compliance
Please send your CV
Michael Bailey International is acting as an Employment Business in relation to this vacancy.