Quality Assurance Manager

Quality Assurance Manager Redmond, WA Job Details Full-time $120,000 - $160,000 a year 1 hour ago Benefits Paid holidays Disability insurance Health insurance Dental insurance Paid time off Vision insurance 401(k) matching Qualifications Quality control corrective actions Regulatory inspections Document review (document control) 7 years Immunological laboratory techniques Regulatory compliance Compliance audits & assessments Laboratory information management systems Corrective and preventive actions (CAPA) Quality management GMP Pathology Immunohistochemistry Master's degree Quality assurance audits Bachelor's degree Laboratory regulatory affairs Quality control documentation Continuous improvement Certified Quality Auditor Scientific protocols Quality improvement CLIA regulations Overseeing audit functions Senior level Cross-functional collaboration Document management systems Leadership Communication skills Regulatory compliance management Cross-functional communication FDA regulations Assays Full Job Description Redmond, WA Full Time Translation Science Experienced SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. We are seeking an experienced Quality Assurance Manager to support our Translational Science department, which includes both Clinical Pathology and Bioanalytical functions. This role is responsible for ensuring compliance with Bioanalytical Lab QA (GLP/FDA) as well as

CLIA/CAP

requirements and partnering closely with scientific and laboratory teams to maintain a robust quality system supporting biomarker, IHC, and bioanalytical assay activities. This is a senior individual contributor QA leadership role with no direct reports. This position is full-time onsite in Redmond, WA and will transition to our new Bothell, WA location in the fall. Key Responsibilities Maintain and improve the Quality Management System (QMS) in compliance with Bioanalytical Lab QA (GLP/FDA) and

CLIA/CAP

across Clinical Pathology and Bioanalytical labs Develop, review, and approve SOPs, protocols, and quality documentation Lead FDA inspection readiness and audits for bioanalytical laboratories, including preparation, hosting, and response management Lead internal audits and inspection readiness for CLIA/CAP and external audits Manage CAPA, deviations, change control, and document control systems Ensure training compliance and documentation across both functional areas Support assay validation, method transfer, and fit-for-purpose biomarker and bioanalytical workflows Partner with translational scientists to ensure quality integration across Clinical Pathology and Bioanalytical operations Track and report quality metrics and drive continuous improvement Serve as QA representative during regulatory inspections and client interactions Qualifications Bachelor's or Master's degree in Life Sciences or related field 7+ years of QA experience in bioanalytical (GLP/FDA) and/or

CLIA/CAP

laboratory environments Strong knowledge of QMS processes (CAPA, deviation, change control, document control) Experience supporting or leading FDA inspections for bioanalytical labs Experience supporting laboratory audits and inspections Familiarity with clinical pathology, bioanalytical, biomarker, or IHC-based workflows preferred Preferred Qualifications Experience in CDx, pathology/IHC, or bioanalytical labs Knowledge of GxP environments (GLP/GCP/GMP) Experience with LIMS and electronic QMS systems ASQ certification (e.g., CQA) is a plus Key Competencies Strong understanding of bioanalytical QA and regulated lab environments Hands-on experience with FDA inspection readiness and audit management Ability to work cross-functionally with scientific and clinical teams Detail-oriented with strong problem-solving and communication skills Why Join Us High-impact role supporting both Bioanalytical and Clinical Pathology functions within Translational Science Opportunity to lead FDA inspection readiness and regulatory excellence Collaborative, science-driven environment

Compensation and Benefits:

The expected base salary range for this position is $120,000 - $160,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's level qualifications, experience, and skills. While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role. SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.