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Pathology Associate Jobs in Everett, WA (NOW HIRING)

Solomon Page

Travel Outpatient Pediatric SLP

Everett, WA · On-site

$1.9K - $2.4K/wk

Speech Pathologists will counsel individuals and their families on ways to improve and support ... Associates can enroll in the 401K plan after they have worked 1000 hours. * ESOP Benefits: As an ...

Uw

Clinical Laboratory Technician 1

Seattle, WA · On-site

$26.33/hr

The UW Medicine - Department of Laboratory Medicine & Pathology (DLMP) in Seattle, WA has a ... Associate or bachelor's degree in science * Experience in a major medical hospital laboratory

Uw

Clinical Laboratory Technician 1

Seattle, WA · On-site

$26.33/hr

The UW Medicine - Department of Laboratory Medicine & Pathology (DLMP) in Seattle, WA has a ... Associate or bachelor's degree in science * Experience in a major medical hospital laboratory

Uw

Clinical Laboratory Technician 1

Seattle, WA · On-site

$26.33/hr

The UW Medicine - Department of Laboratory Medicine & Pathology (DLMP) in Seattle, WA has a ... Associate or bachelor's degree in science * Experience in a major medical hospital laboratory

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Pathology Associate information

See Everett, WA salary details

$11

$21

$36

How much do pathology associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for pathology associate in Everett, WA is $21.95, according to ZipRecruiter salary data. Most workers in this role earn between $16.44 and $22.84 per hour, depending on experience, location, and employer.

What is a pathology associate?

Pathology Associates are professionals who assist pathologists in the examination and analysis of tissue, blood, and other body fluid samples to help diagnose diseases. They typically prepare specimens, operate laboratory equipment, and document results for review by a pathologist. Pathology Associates may work in hospitals, research laboratories, or clinics and play a crucial role in ensuring accurate test results and maintaining laboratory safety standards. Their work supports the diagnosis and treatment of patients by providing essential data to medical teams.

What does a pathology associate do?

A Pathology Associate typically assists with specimen preparation, labeling, and documentation, ensuring samples are processed accurately and efficiently. They work closely with pathologists by preparing slides, maintaining laboratory equipment, and occasionally compiling preliminary data. Collaboration with laboratory technologists and administrative staff is essential to ensure smooth workflow and adherence to safety protocols. Clear communication and attention to detail are crucial, as errors can impact diagnostic outcomes for patients.

What skills and qualifications are needed to be a pathology associate?

To thrive as a Pathology Associate, you need a solid background in biological sciences, laboratory techniques, and typically a bachelor’s degree in a related field. Familiarity with laboratory information management systems (LIMS), microscopy, and safety protocols is crucial, and certifications such as ASCP can be advantageous. Attention to detail, problem-solving abilities, and effective communication are important soft skills for collaborating with pathologists and ensuring accurate results. These skills and qualifications are vital to maintain high standards of laboratory accuracy, reliability, and safety in diagnostic processes.

Associate Director / Director, Regulatory Affairs - IHC Companion Diagnostics (CDx)

SystImmune, Inc

Redmond, WA • On-site

$150K - $230K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 days ago

Job description

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 a Regulatory Affairs leader at the Associate Director or Director level to lead IHC-based Companion Diagnostics (CDx) regulatory strategy and execution in support of our oncology ADC pipeline. This role will serve as the regulatory authority for CDx programs, with direct FDA CDRH engagement, and will build and lead a growing CDx Regulatory team over time.
The successful candidate will set regulatory direction, guide cross-functional teams, and ensure high-quality IDE and PMA submissions, while remaining sufficiently hands-on to provide technical oversight and mentorship when needed. This position reports directly to the Head of CDx and is a core leadership role in the CDx organization.
Key Responsibilities
CDx Regulatory Leadership
  • Lead US regulatory strategy for IHC-based Companion Diagnostics across multiple oncology programs
  • Serve as the regulatory decision-maker for CDx development, submissions, and FDA engagement
  • Establish CDx regulatory best practices, processes, and governance within the organization
FDA CDRH Engagement & Representation
  • Act as the senior regulatory representative to FDA CDRH for IHC CDx programs
  • Lead FDA Pre-Submission (Q-sub), IDE, and PMA interactions at a strategic and executional level
  • Guide preparation of FDA briefing packages and responses, ensuring scientific and regulatory consistency
Team Building & People Leadership
  • Build, mentor, and lead a CDx Regulatory Affairs team, with direct reports added over time
  • Set expectations, review work quality, and develop regulatory talent within the CDx organization
  • Provide regulatory leadership and mentorship to cross-functional partners and junior team members
Cross-Functional & External Leadership
  • Partner with Drug Regulatory (CDER), Clinical Development, Biomarker, Pathology, and QA leaders to ensure aligned drug-diagnostic co-development
  • Lead regulatory coordination with external diagnostic partners, CROs, and central laboratories
  • Represent CDx Regulatory perspectives in senior cross-functional and program governance meetings
Submission Oversight & Quality
  • Provide leadership oversight for IDE, PMA, and PMA supplement submissions for IHC CDx
  • Ensure analytical and clinical performance strategies (including scoring and cutoff rationale) meet FDA expectations
  • Maintain high regulatory quality standards while enabling efficient execution
Risk Management & Readiness
  • Identify and proactively manage regulatory risks related to IHC assay performance, interpretation, and transfer
  • Support inspection readiness and regulatory compliance for CDx partners and internal processes
  • Monitor evolving FDA CDx and IHC-related guidance and assess impact on portfolio strategy

Qualifications
  • Bachelor's degree or higher in Life Sciences, Pathology, Molecular Biology, or related field
  • 8+ years (Associate Director) or 10+ years (Director) of regulatory affairs experience in IVD/CDx
  • Demonstrated experience leading FDA CDRH interactions for Companion Diagnostics
  • Strong background in IHC-based CDx development, including understanding of scoring systems and clinical cutoffs
  • Proven ability to lead cross-functional teams and influence without authority

Preferred
  • Prior experience managing or building regulatory teams
  • Oncology CDx experience supporting patient selection strategies
  • Experience working with automated IHC platforms and external diagnostic partners
  • Familiarity with global CDx regulations (EU IVDR, China NMPA)

Leadership Competencies
  • Strategic decision-making with execution awareness
  • Clear, confident FDA-facing communication
  • Ability to develop people and build scalable regulatory functions
  • Strong judgment balancing regulatory rigor with program timelines

Compensation and Benefits:
The expected base salary range for this position is $150,000 - $230,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's qualifications, experience, and skills.
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.

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