Raw Materials Process Development & Validation Specialist
Listed on 2026-10-12
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Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Avecia Pharma is seeking a Process Development Validation-Raw Material Associate in Milford, MA. In this role you will support the chemical raw material onboarding programs, manage material databases, and contribute to vendor assurance activities within cGMP guidelines.
You will help develop and review raw material specifications, support material release testing data analysis, and coordinate SAP-based inventory workflows while maintaining compliance and thorough technical documentation.
Join us at Avecia Pharma as our next Raw Materials Process Development & Validation Specialist in Milford, MA, United States.
This posting is for the Raw Materials Process Development & Validation Specialist role at Avecia Pharma, based in Milford, MA, United States.
We are looking to fill the Raw Materials Process Development & Validation Specialist position at Avecia Pharma in Milford, MA, United States.
The Raw Materials Process Development & Validation Specialist role at Avecia Pharma is now open for applications in Milford, MA, United States.
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