CSV / Automation Consultant
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Role details
Tech stack
Requirements
We are looking for an experienced CSV / Automation Consultant with a strong background in the pharmaceutical or life sciences industry to support a 5-6-month project in Massachusetts.
The ideal candidate will have hands-on experience with Computer System Validation (CSV), automation systems, and compliance requirements in regulated pharmaceutical manufacturing environments.
Required Skills & Qualifications
Experience in Computer System Validation (CSV) and/or automation within the pharmaceutical industry.
Strong knowledge of cGMP/GxP regulations and regulated manufacturing environments.
Experience preparing and executing validation documentation, protocols, test scripts, and compliance activities.
Ability to troubleshoot automation systems and validation-related issues.
Strong documentation, communication, analytical, and problem-solving skills.
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Prepare application
- Draft this with your agent
- Open in Claude
- Open in ChatGPT
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