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Regulatory affairs specialist - medical device manufacturing
Regulatory affairs specialist / RA specialist / Regulatory affairs professional required for an immediate 4 month contract within the medical device / ISO 13485 manufacturing industry.
Professionals from a ISO 13485 / medical device must have worked specifically within regulatory / RA roles as opposed to quality or validation engineering work...View full job description
From CV Library
- 06 Feb 2012
Professionals from a ISO 13485 / medical device must have worked specifically within regulatory / RA roles as opposed to quality or validation engineering work...View full job description
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