Senior QA Specialist – Onsite GMP Compliance & Release
Listed on 2026-10-18
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Quality Assurance - QA/QC
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Healthcare
Kiniksa Pharmaceuticals, based in Lexington, MA, is seeking a Specialist/Sr. Specialist, QA to provide QA support for manufacturing, QC, and analytical development, ensuring batch disposition and regulatory compliance.
This role requires onsite presence five days a week. Responsibilities include reviewing GMP documentation, batch records, regulatory data, and collaborating with CDMOs and internal teams to maintain data integrity and quality systems.
This posting is for the Senior QA Specialist – Onsite GMP Compliance & Release role at Regulatory Jobs, based in Lexington, MA, United States.
The following opening is for a Senior QA Specialist – Onsite GMP Compliance & Release with Regulatory Jobs.
Our group is growing, and we are hiring a Senior QA Specialist – Onsite GMP Compliance & Release in Lexington, MA, United States.
This opening is for the Senior QA Specialist – Onsite GMP Compliance & Release role at Regulatory Jobs.
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