QA Specialist

For our client in Basel, we are seeking QA Specialist for a Drug Supply Management project

Start Date: 1st July 2015
End Date: 30th June 2016
Languages: English (and German is preferred)

Key Deliverables:

Manage a portfolio of projects
Review and recommend disposition of deliverables and related tools to ensure GMP compliance
Support project related activities and project management functions
Perform inspections and audits as required
Contribute to the evaluation of new QA tools
Write GMP relevant documents in own area of responsibility - eg SOPs with global applicability
Provide support to TRD line functions in GMP compliance related issues
Meet internatl and external guality and safety guidelines

Skills/Experience:

Education: Bachelor degree in scientific/relevant discipline; Masters degree or above is preferred
Ability to analyse and evaluate GMP compliance
Ability to negotiate and communicate
Sound scientific, technical and regulatory knowledge
Excellent knowledge of cGMPs, working knowledge of safety and environment regulations & guidelines
Good knowledge of drug development
Good organizational skills Michael Bailey International is acting as an Employment Business in relation to this vacancy.