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Senior Qa Jobs in Bothell, WA (NOW HIRING)

LeonaBio, Inc.

Quality Assurance Manager

Bothell, WA · On-site

$130K - $145K/yr

Reporting directly to the Senior Director of Quality, this role ensures the integrity, consistency ... Lead QA support and provide strategic quality oversight for outsourced cGMP operations related to ...

LeonaBio, Inc.

Quality Assurance Manager

Bothell, WA · Remote

Reporting directly to the Senior Director of Quality, this role ensures the integrity, consistency ... Lead QA support and provide strategic quality oversight for outsourced cGMP operations related to ...

B.E. Meyers

Quality Assurance Specialist

Redmond, WA · On-site

$28 - $31/hr

Quality Assurance Specialist Department: Quality Reports To: Quality Manager SUMMARY: The Quality ... Ability to effectively present information and respond to questions from the Senior Management Team ...

OSI Systems, Inc

Sr. Manager Quality

Snoqualmie, WA · On-site

$165K - $185K/yr

The Senior Quality Assurance Manager manages quality system processes, internal audits, corrective action preventive action (CARs and PARs), change control, quality system software validations and ...

Omeros

Manager, Clinical QA

Seattle, WA · On-site

We are a fast-growing and dynamic organization seeking a Clinical QA Manager/Sr Manager to join our Reg QA team. This position provides quality and compliance oversight and performs a wide variety of ...

Omeros Corp.

Manager, Clinical QA

Seattle, WA · On-site

We are a fast-growing and dynamic organization seeking a Clinical QA Manager/Sr Manager to join our Reg QA team. This position provides quality and compliance oversight and performs a wide variety of ...

B.E. Meyers

Quality Assurance Technician

Redmond, WA · On-site

$32 - $36/hr

Quality Assurance Technician Department: Quality Reports To: Quality Manager SUMMARY: The Quality ... Ability to effectively present information and respond to questions from the Senior Management Team ...

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Senior Qa information

What is the difference between Senior Qa vs Quality Assurance Analyst?

AspectSenior QaQuality Assurance Analyst
CredentialsTypically requires 5+ years experience, certifications like ISTQB or CSTEUsually 2-4 years experience, similar certifications
Work EnvironmentLeads testing teams, involved in planning and strategyPerforms testing, reports bugs, executes test cases
Industry UsageUsed across software, hardware, and systems industriesPrimarily in software development and IT sectors

Senior Qa roles generally involve more leadership, strategic planning, and mentorship compared to Quality Assurance Analysts, who focus on executing tests and reporting issues. The Senior Qa often oversees testing processes, while QA Analysts perform the hands-on testing tasks.

What is a senior QA?

Senior QA (Quality Assurance) engineers are experienced professionals responsible for ensuring that software products meet quality standards before release. They design and execute test plans, identify bugs, and work closely with development teams to resolve issues. Senior QA engineers often mentor junior team members, develop automated testing frameworks, and contribute to the overall improvement of testing processes. Their role is critical in delivering reliable and high-performing software products.

What is the average salary for a senior QA tester?

The average salary for a senior QA tester typically ranges from $70,000 to $110,000 annually, depending on experience, location, and industry. Senior QA professionals often have expertise in automation tools and testing frameworks, which can influence compensation levels.

How does a senior QA typically collaborate with development and product teams during a software release cycle?

A Senior QA works closely with both development and product teams throughout the software release cycle to ensure quality standards are met. They participate in sprint planning, clarify acceptance criteria, and provide input on testability during design discussions. Senior QAs also coordinate with developers to identify, reproduce, and resolve defects, and often lead the testing effort by mentoring junior team members. Their proactive communication helps ensure that issues are caught early and that releases proceed smoothly.

What are the key skills and qualifications needed to thrive as a senior QA, and why are they important?

To thrive as a Senior QA, you need strong analytical skills, experience with software testing methodologies, and a background in computer science or a related field. Familiarity with test automation tools (such as Selenium or JUnit), bug tracking systems (like Jira), and relevant certifications (e.g., ISTQB) is highly valuable. Excellent communication, attention to detail, and problem-solving abilities set top performers apart in this role. These skills ensure high-quality software releases, effective collaboration with development teams, and efficient identification and resolution of issues.

Is senior QA still in demand?

Senior QA professionals are in continued demand due to the ongoing need for quality assurance in software development. They often require expertise in testing tools, automation, and industry standards, with opportunities across various industries including technology, finance, and healthcare.

What are the most commonly searched types of Qa jobs in Bothell, WA?

The most popular types of Qa jobs in Bothell, WA are:

What cities near Bothell, WA are hiring for Senior Qa jobs?

Cities near Bothell, WA with the most Senior Qa job openings:

Senior Qa jobs near you
Infographic showing various Senior Qa job openings in Bothell, WA as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 80% Full Time, 11% Part Time, 6% Contract, and 1% Nights. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution.

Quality Assurance Manager

LeonaBio, Inc.

Bothell, WA • On-site

$130K - $145K/yr

Full-time

Re-posted 28 days ago

Job description

About LeonaBio:
LeonaBio, Inc., headquartered in the Seattle, Washington area, is a clinical-stage biopharmaceutical company dedicated to the development of novel therapeutics for high unmet medical needs, including amyotrophic lateral sclerosis (ALS) and treatment-resistant metastatic breast cancer, with the goal of improving patients' lives. Our lead drug candidates, lasofoxifene and ATH-1105, are novel, small molecule therapies with the potential to address devastating diseases where current treatment options are limited or ineffective. With a strong commitment to scientific excellence and patient-centered innovation, we are dedicated to developing meaningful new therapies for those who need them most.
About this role:
The Quality Assurance Manager plays a critical role in supporting and strengthening LeonaBio's Quality Assurance function. Reporting directly to the Senior Director of Quality, this role ensures the integrity, consistency, and continuous improvement of quality systems across the organization. The ideal candidate brings strong analytical skills, a proactive mindset, and the ability to partner effectively with cross-functional teams to uphold high standards of quality and compliance.
Responsibilities:
  • Lead QA support and provide strategic quality oversight for outsourced cGMP operations related to the manufacture of drug product used in clinical trials.
  • Lead the review of executed batch records and ancillary documentation to ensure accuracy, completeness, compliance with approved procedures, and readiness for disposition decisions.
  • Oversee and perform product disposition activities for clinical trial materials, ensuring decisions are well documented, risk-based, and aligned with quality and regulatory expectations.
  • Provide QA review and approval for Master Batch Records, protocols, reports, and SOPs, ensuring alignment with internal standards, phase-appropriate regulations, and operational needs.
  • Support and help coordinate computer system validation activities as needed to maintain compliant and effective quality-related systems.
  • Lead the QA review of deviations, product non-conformities, and other investigations to ensure robust root cause analysis, timely resolution, and sustained compliance.
  • Oversee CAPA review and closure activities, ensuring proposed actions are appropriate, effectively implemented, and supported by meaningful effectiveness checks.
  • Provide oversight of change controls and periodic reviews of controlled documents to ensure changes are appropriately assessed, approved, and implemented within the quality system.
  • Support oversight of the training program to help ensure training assignments, completion, and compliance are maintained across applicable quality processes.
  • Author, revise, and approve quality documentation as needed, while driving clarity, consistency, and compliance across documentation practices.
  • Analyze and report quality-related metrics to identify trends, inform risk-based decisions, and support continuous improvement initiatives.
  • Support regulatory audits and inspections by helping prepare the organization, coordinating quality inputs, and assisting with timely follow-through on observations and commitments.
  • Support the external audit process by scheduling, preparing, and performing GCP, GCLP, GLP, and GMP supplier audits with follow-through on completing the audit report and receiving a timely response, as applicable, from the supplier.
  • Support the internal audit process by scheduling, preparing, and performing, or supporting, the audit while assisting with timely follow-through for audit reports and/or responses.
  • Contribute to additional quality and cross-functional initiatives, special projects, and operational priorities as assigned.

Requirements:
  • Bachelor's degree in a life science field.
  • Minimum of 5 years of experience in the pharmaceutical industry plus working knowledge and understanding of GxPs for drugs in development.
  • Experience performing GCP, GCLP, GLP, and GMP audits a plus.
  • Ability to maintain attention to detail, prioritize work, and handle multiple assignments in a fast-paced environment.
  • Ability to critically evaluate and troubleshoot complex problems, while offering timely and informed options for resolution.
  • Ability to adapt the work schedule to participate in teleconferences with CDMOs and CROs in different time zones.
  • Must have excellent verbal, written, and organizational skills.
  • Must have excellent leadership and interpersonal skills with the ability to effectively interact and influence different functional groups at all levels of management.
  • Experience with Veeva and SharePoint a plus.
  • Travel within the US will be required on occasion. Travel outside of the US may be required.
  • Must be authorized to work in the United States; visa sponsorship is not available for this role

LeonaBio is an equal opportunity employer and does not unlawfully discriminate against employees or applicants for employment on the basis of an individual's race, color, religion, creed, sex, national origin, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline and termination.

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