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Extraction Lab Manager Jobs in Oregon (NOW HIRING)

Extract empirical evidence from early commercial and Laboratory Developed Test (LDT) cohorts to ... R&D, commercial, medical, and lab operations functions * Strong ownership mindset with the ...

Cell-Based Assay Scientist

Beaverton, OR · On-site

$36.75 - $46/hr

Travel to conferences, customer sites, workshops and/or open lab events in support of sales ... Competency in basic file management operations on both Windows and MacOS platforms. Proficiency in ...

Cell-Based Assay Scientist

Beaverton, OR · On-site

$36.75 - $46/hr

Travel to conferences, customer sites, workshops and/or open lab events in support of sales ... Competency in basic file management operations on both Windows and MacOS platforms. Proficiency in ...

Showing results 41-43

Extraction Lab Manager information

What is the difference between Extraction Lab Manager vs Extraction Technician?

AspectExtraction Lab ManagerExtraction Technician
CredentialsRelevant certifications, management experienceTechnical certifications, training in extraction processes
Work EnvironmentSupervisory role in lab setting, overseeing operationsHands-on extraction work, operating equipment
Industry UsageUsed in labs, production facilities, overseeing extraction teamsPerforms extraction tasks under supervision

The Extraction Lab Manager typically oversees extraction operations, manages staff, and ensures quality control, requiring management skills and relevant certifications. In contrast, the Extraction Technician focuses on executing extraction procedures, operating equipment, and maintaining safety protocols. Both roles are essential in extraction labs but differ mainly in responsibility level and scope of work.

What are the key skills and qualifications needed to thrive as an extraction lab manager, and why are they important?

To thrive as an Extraction Lab Manager, you need a solid background in chemistry or biochemistry, experience with extraction processes, and often a relevant degree or certification. Proficiency with laboratory equipment, extraction technologies (such as CO2 or ethanol extraction), and familiarity with regulatory compliance systems like GMP are typically required. Strong leadership, attention to detail, and effective communication skills help ensure team coordination and adherence to safety protocols. These skills and qualifications are critical for maintaining product quality, regulatory compliance, and efficient lab operations.

What is an extraction lab manager?

Extraction Lab Managers are professionals responsible for overseeing the extraction of compounds from raw materials, commonly in industries like pharmaceuticals, food and beverage, and cannabis. They manage the daily operations of extraction labs, ensure compliance with safety and regulatory standards, supervise staff, and optimize extraction processes for efficiency and quality. Their role also includes maintaining equipment, managing inventory, and ensuring all products meet quality control standards. Extraction Lab Managers often have backgrounds in chemistry, biology, or related fields and play a key role in product development and process improvement.

What are some common challenges faced by an extraction lab manager in maintaining compliance with safety and regulatory standards?

Extraction Lab Managers often encounter challenges in ensuring their operations strictly adhere to evolving safety and regulatory requirements, especially in industries like cannabis or pharmaceuticals. They must stay updated on local, state, and federal regulations, conduct regular staff training on safety protocols, and maintain meticulous documentation for audits. Balancing efficient production with rigorous compliance can be demanding, but proactive communication, continuous process improvement, and a strong safety culture help mitigate these challenges.
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Infographic showing various Extraction Lab Manager job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 2% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution.

Associate Director, Real-World Evidence & Epidemiology

Natera

OR

Full-time

Posted 7 days ago


Natera rating

7.6

Company rating: 7.6 out of 10

Based on 37 frontline employees who took The Breakroom Quiz

60th of 120 rated laboratories


Job description

POSITION SUMMARY:

We are seeking a Principal Clinical Scientist / Associate Director of Real-World Evidence & Epidemiology to drive observational evidence strategy for our Early Cancer Detection (ECD) portfolio. Population-scale liquid biopsy screening requires robust real-world evidence demonstrating clinical utility, clinical decision-making impact, and downstream patient outcomes. This ownership role uses real-world datasets to accelerate standard-of-care implementation across oncology diagnostics. Working with a builder mindset, you will partner across Clinical Science, Medical Affairs, Market Access, and Data Science to convert population-scale observational data into actionable clinical implementation strategies.

PRIMARY RESPONSIBILITIES:

Epidemiology and Observational Research Strategy

  • Lead the design, protocol development, and execution of prospective observational studies, registries, and retrospective database assessments across early cancer detection programs
  • Shape post-market evidence generation strategies by isolating critical clinical utility and implementation hurdles that can be resolved via real-world data assets
  • Translate clinical and market requirements into rigorous, practical study designs, specifying target populations, clinical endpoints, and analytic frameworks
  • Systematically identify and mitigate sources of bias, confounding factors, and missing data variance inherent in real-world healthcare datasets
  • Design protocols evaluating clinical utility across diverse populations, ensuring the data generated directly supports precision interventions for individual patients and families

Cross-Functional Scientific Leadership

  • Partner across Clinical Science, Medical Affairs, Product Management, and Market Access to prioritize evidence generation initiatives based on regulatory and clinical urgency
  • Collaborate with Biostatistics and Data Science to engineer statistical analysis plans, interpret data findings, and deliver clinical contextualization
  • Extract empirical evidence from early commercial and Laboratory Developed Test (LDT) cohorts to isolate adoption variables, diagnostic compliance, and real-world clinical workflows
  • Deliver real-world data assets that dismantle payer coverage barriers and ground product positioning strictly in clinical utility metrics

Evidence Dissemination and External Engagement

  • Convert complex epidemiological findings into clear, high-integrity scientific narratives for internal product governance and external healthcare stakeholders
  • Spearhead the development of peer-reviewed abstracts, posters, presentations, and core manuscripts for major oncology and diagnostic conferences
  • Engage with external clinical collaborators, investigators, and key opinion leaders (KOLs) to advance the platform base for early cancer detection

QUALIFICATIONS:

  • Advanced degree (PhD, MPH, MS, PharmD, or equivalent scientific credential) in epidemiology, health outcomes research, biostatistics, or a highly quantitative field
  • 7+ years of experience leading real-world evidence generation, observational clinical research, or HEOR portfolios within the life sciences industry
  • Documented experience executing observational studies across the entire asset lifecycle, from initial protocol drafting through statistical analysis and publication
  • Deep data competency across real-world data sources, including longitudinal medical claims, electronic health records (EHR), and clinical registries
  • Direct experience in oncology clinical trials, molecular diagnostics, or early cancer detection programs is preferred

KNOWLEDGE, SKILLS, AND ABILITIES:

  • Take full ownership of complex clinical portfolios as an autonomous strategist
  • Rigorous analytical skills with the ability to pressure-test study assumptions and ground major milestones entirely in data
  • Communicate with technical precision across matrixed lines to align R&D, commercial, medical, and lab operations functions
  • Strong ownership mindset with the capability to balance scientific rigor, speed, and trial resource constraints under tight timelines
  • Comfort with ambiguity and an evolving product surface as underlying genomic science advances

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