DeltaV Validation Engineer – FDA QA/CSV Specialist
Listed on 2026-10-09
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Quality Assurance - QA/QC
Quality Engineering -
Engineering
Quality Engineering
ADVENT Engineering in Boston, MA seeks an experienced Validation Engineer to join our pharmaceutical and biotech project teams. You will draft and implement quality system documentation, author URS/IQ/OQ/PQ protocols, and design validation strategies across GMP facilities.
Responsibilities include data integrity assessments, 21 CFR Part 11 compliance, and collaboration with R&D and Manufacturing to support tech transfer and continuous improvement.
The following opportunity is for a DeltaV Validation Engineer – FDA QA/CSV Specialist with Trinity Consultants
- Advent Engineering.
The following position is for a DeltaV Validation Engineer – FDA QA/CSV Specialist with Trinity Consultants
- Advent Engineering.
Our team is growing, and we are hiring a DeltaV Validation Engineer – FDA QA/CSV Specialist in Boston, MA, United States.
This position is for the DeltaV Validation Engineer – FDA QA/CSV Specialist role at Trinity Consultants
- Advent Engineering.
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