Randstad USA is seeking a QA Documentation Specialist in Portsmouth, NH. This role is critical for supporting Quality System Management and involves managing document control processes in a compliance-driven environment.
The position requires 1-3 years of quality experience in the pharmaceutical industry, with a focus on GMP and QA practices. Contract duration is 6 months, and work is exclusively on-site, Monday to Friday, from 9 AM to 5 PM, with competitive salary offerings.
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QA Documentation Specialist (Contract) - Veeva
Randstad · Portsmouth, NH, USA ·
- Job type:
- Contract