About this opportunity
Regulatory Jobs lists this Senior QA Specialist – Onsite GMP Compliance & Release opportunity in lexington, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
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Worksite address
lexington, MA, 02173, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.