Specialist​/Senior Specialist - Quality Assurance

Position: Specialist / Senior Specialist - Quality Assurance
Kiniksa Pharmaceuticals is a commercial‑stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, with a focus on cardiovascular indications. With deep expertise in immunology and inflammation, Kiniksa is advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST, the first and only FDA‑approved therapy for recurrent pericarditis. Grounded in rigorous science and bold innovation, the company fosters a highly collaborative, patient‑first culture led by accomplished life sciences leaders.

At Kiniksa, talented individuals are trusted and empowered to make a real impact—shaping the future of medicine while improving the lives of patients who need it most.

The Specialist/Sr. Specialist, QA is recognized as a subject matter expert in the application of quality assurance and compliance. The incumbent will provide QA support for internal/external manufacturing and laboratory operations, quality control, analytical development in support of batch disposition activities. The incumbent will perform review of drug substance/drug product/finished drug product manufacturing records and associated documents (e.g. Deviations, change controls, investigations, supplier change notifications) for products that will be released for use in Kiniksa programs.

This role is based in our Lexington, MA office and requires employees to be onsite five days per week.

Responsibilities (including, but not limited to):

Oversee quality operations at Kiniksa and at external service providers (CDMO’s/CTL’s)
Review and approve service provider’s GMP documentation

Review and approve master/executed batch records, packaging records for, drug substances, drug product/finished drug product

Perform GMP raw material release activities for Kiniksa internal manufacturing operations

Review and approve laboratory data related to release and stability of GMP materials, qualification of test methods and reference standards, including protocols, data and reports

Collaborate with external service providers and internally with QA, RA, CMC teams to support the timely review and approval of documents

Review records including audit trails and ensure integrity of data and results generated by Kiniksa and external CDMO’s/CTL’sSupport batch disposition activities, including data upload, review, and documentation in applicable quality systems

Compile data for Quality system reviews

Evaluate and support GMP activities for continuous improvement

Other Quality Assurance responsibilities as assigned

Standout Skills for Impact:

QA experience in a GMP-regulated environment

Experience with Veeva Quality Docs and Veeva QMSExcellent verbal and written communication skills with proven track record of communication with internal and external service providers

Knowledge of industry standards, current GMP (21

CFR Parts 210 & 211 & Part 11 and Eudra Lex) and other agency standards

Qualifications and

Experience:

Bachelors in a scientific discipline with 4+ years of experience in the FDA regulated pharmaceutical/biotech industry with GMP manufacturing operations analytical development and quality

Experience in Biologics and Combination Products (Cell and Gene Therapy, monoclonal antibodies) is preferred

Experience with review of GMP manufacturing records (Master/Executed batch records, change controls, deviations, investigations, change controls, product complaints) associated with clinical programs

Hands-on experience with laboratory testing and method validation

Familiarity with a wide range of test methods needed for evaluation of diverse samples, such as cell banks, drug substance, drug product, and combination products is a plus Strong team player that has a customer…