We are seeking an experienced Quality Assurance Manager to join a growing translational science organization within a well-funded clinical-stage biotechnology company focused on innovative oncology therapeutics. This individual will play a critical role in supporting both Clinical Pathology and Bioanalytical functions, ensuring quality and compliance across regulated laboratory operations. This is a high-impact, senior individual contributor role suited for someone who is hands-on, detail-oriented, and experienced in regulated bioanalytical and laboratory QA environments. The ideal candidate will enjoy partnering cross-functionally with scientific teams and helping strengthen quality systems that support biomarker, IHC, and bioanalytical assay activities.

Location:

Redmond, WA (onsite; transitioning to Bothell, WA in the fall)

Type:

Full Time Compensation:

Base salary $120,000-$160,000 (DOE)

Industry:

Biotechnology What You'll Do:

Maintain and improve the Quality Management System (QMS) across Clinical Pathology and Bioanalytical labs in compliance with Bioanalytical Lab QA (GLP/FDA) and

CLIA/CAP

requirements Develop, review, and approve SOPs, protocols, and other quality documentation Lead FDA inspection readiness and support bioanalytical lab audits, including preparation, hosting, and response management Lead internal audits and inspection readiness activities 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 closely with translational scientists to integrate quality across Clinical Pathology and Bioanalytical operations Track and report quality metrics and drive continuous improvement initiatives Serve as QA representative during regulatory inspections and client interactions

What We're Looking For:

Bachelor's or Master's degree in Life Sciences or a related field 7+ years of QA experience in bioanalytical (GLP/FDA) and/or

CLIA/CAP

laboratory environments Strong knowledge of QMS processes, including CAPA, deviations, change control, and document control Experience supporting or leading FDA inspections for bioanalytical labs Experience supporting laboratory audits and inspections Ability to work cross-functionally with scientific and clinical teams Strong problem-solving, communication, and organizational skills Comfortable in a hands-on senior individual contributor role with no direct reports Nice to

Have:

Experience in CDx, pathology/IHC, or bioanalytical lab settings Knowledge of GxP environments, including GLP, GCP, and GMP Experience with LIMS and electronic QMS systems ASQ certification such as

CQA Work Environment:

Collaborative, science-driven team environment High-visibility role supporting both Bioanalytical and Clinical Pathology within Translational Science Opportunity to lead inspection readiness and strengthen regulatory excellence Standard onsite work environment with close partnership across laboratory and scientific teams #

IND-SPG Estimated Min Rate:

$120,000

Estimated Max Rate:

$160,000 What's In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements.

Benefits include:

Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week) Health Savings Account (HSA) (for employees working 20+ hours per week) Life & Disability Insurance (for employees working 20+ hours per week) MetLife Voluntary Benefits Employee Assistance Program (EAP) 401K Retirement Savings Plan Direct Deposit & weekly epayroll Referral Bonus Programs Certification and training opportunities

Note:

Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit https:

//www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our

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