Specialist / Senior Specialist - Quality Assurance

Kiniksa Pharmaceuticals•Lexington, KY

3d•Onsite

About The Position

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.

Requirements

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 service approach and is solution oriented
Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external service providers in a professional and collaborative manner
QA experience in a GMP-regulated environment
Experience with Veeva QualityDocs and Veeva QMS
Excellent verbal and written communication skills with proven track record of communication with internal and external service providers
Knowledge of industry standards, current GMP (21CFR Parts 210 & 211 & Part 11 and EudraLex) and other agency standards

Responsibilities

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’s
Support 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