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I've started a preliminary search for a Biotech Quality Systems
consultant who can help me research and write some of our Corporate
Standards and Guides.
I'm looking for someone with experience in:
- Implementing ISO 9000 or similar systems
- Thorough knowledge of computer, process, and assay validation
principles along with other technical knowledge on such issues
as water systems and HEPA filters.
- Knowledge of cGMPs for Diagnostics and Therapeutics
- Knowledge of documentation management systems
- Ability to coordinate and work with various levels of management
in different countries
- Technical writing skills, MS Word and WordPerfect experience.
I expect this to be approximately a two- to three-month position.
Any help would be appreciated.
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