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Quality Assurance Biotech Jobs in Bothell, WA (NOW HIRING)

ELITechGroup Inc.

Quality Assurance Associate

Bothell, WA · On-site

$30 - $32/hr

A successful biotech company is looking for an experienced and detail-oriented Associate to join our Quality Assurance team on site in Bothell, WA. Unfortunately at this time no relocation or visa ...

Systimmune

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

We are seeking an experienced Quality Assurance Manager to support our Translational Science ... SystImmune is a leading and well-funded biotech company with a bright future. We offer an ...

SystImmune, Inc

Quality Assurance Manager

Redmond, WA · On-site

$120K - $160K/yr

We are seeking an experienced Quality Assurance Manager to support our Translational Science ... SystImmune is a leading and well-funded biotech company with a bright future. We offer an ...

Omeros Corp.

Manager, Clinical QA

Seattle, WA · On-site

Omeros is an innovative biotechnology company that discovers and develops first-in-class protein ... Provide support and proactive, strategic planning for QA oversight of clinical development ...

Omeros

Manager, Clinical QA

Seattle, WA

Omeros is an innovative biotechnology company that discovers and develops first-in-class protein ... Provide support and proactive, strategic planning for QA oversight of clinical development ...

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Quality Assurance Biotech information

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How much do quality assurance biotech jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for quality assurance biotech in Bothell, WA is $33.18, according to ZipRecruiter salary data. Most workers in this role earn between $21.25 and $38.94 per hour, depending on experience, location, and employer.

What is a Quality Assurance Biotech job?

A Quality Assurance (QA) Biotech job involves ensuring that biotechnology products meet regulatory and company standards for safety, efficacy, and quality. QA professionals develop and implement quality systems, conduct audits, review documentation, and ensure compliance with Good Manufacturing Practices (GMP) and other regulations. They collaborate with various departments, including manufacturing, R&D, and regulatory affairs, to maintain product integrity. Their role is critical in preventing defects, ensuring consistent processes, and maintaining compliance with industry standards.

What are the key skills and qualifications needed to thrive in the Quality Assurance Biotech position, and why are they important?

To thrive as a Quality Assurance Biotech, you need a solid understanding of biotechnology processes, quality control methodologies, and regulatory standards such as GMP, often supported by a degree in biology, chemistry, or a related field. Familiarity with laboratory information management systems (LIMS), documentation software, and industry certifications like ASQ or GMP training is highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills are valued soft skills in this role. These abilities ensure precise compliance with regulatory requirements, facilitate collaboration with cross-functional teams, and help maintain the integrity and safety of biotech products.

What are the most common challenges faced by Quality Assurance professionals in the biotech industry?

Quality Assurance professionals in biotechnology often encounter challenges related to staying up-to-date with evolving regulatory requirements and ensuring that all processes consistently meet strict quality standards. Additionally, managing thorough documentation and collaborating across various departments—such as research, manufacturing, and regulatory affairs—can be complex. Those in the role may also need to respond quickly to deviations or quality events, requiring both proactive problem-solving and excellent organizational skills. However, overcoming these challenges is highly rewarding, as it directly contributes to maintaining the safety and efficacy of biotech products.

What are popular job titles related to Quality Assurance Biotech jobs in Bothell, WA? For Quality Assurance Biotech jobs in Bothell, WA, the most frequently searched job titles are:
What job categories do people searching Quality Assurance Biotech jobs in Bothell, WA look for? The top searched job categories for Quality Assurance Biotech jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Quality Assurance Biotech jobs? Cities near Bothell, WA with the most Quality Assurance Biotech job openings:
Quality Assurance Biotech jobs near you
Infographic showing various Quality Assurance Biotech job openings in Bothell, WA as of July 2026, with employment types broken down into 1% As Needed, 88% Full Time, 8% Part Time, and 3% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $68,107 per year, or $32.7 per hour.

Quality Assurance Associate at Biotech Company-Bothell, WA

Epoch BioSciences

Seattle, WA • On-site

Full-time

Posted 19 days ago

Job description

A successful biotech company is looking for an experienced and detail-oriented Associate to join our Quality Assurance team on site in Bothell, WA. Unfortunately at this time no relocation or visa sponsorship provided.

At ELITechGroup, we are committed to supporting health systems globally. We take pride in our team and strive to maintain a work environment that is both professionally challenging and personally fulfilling. As a valued member of our team, you would contribute to the manufacturing and distribution of in vitro diagnostic products to clients in over 100 countries. You will have the opportunity to work alongside some of the brightest minds in the industry, as our team is dedicated to solving problems and delivering excellent products. This position is ideal for someone with some experience in the biotech industry and audits, who takes pride in learning all aspects of the job and adhering to procedures and standards. You will receive guidance from a supportive team that will ensure you are trained and capable of performing your responsibilities effectively. The primary focus of the QA Associate role is to support commercial production to ensure consistent compliance with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused culture by ensuring documentation is complete, accurate and that Batch records are executed in accordance with approved and effective standard operating procedures and specifications.

Summary

With direction, has part of the responsibility for ELITechGroup MDx Quality Assurance activities.

Essential Duties and Responsibilities

  • Performs review of manufacturing batch records, enter information in Disposition Log, filing of batch records, and ensure the records are complete and stored in a manner where they are readily retrievable.
  • Performs finished product inspection.
  • Performs review and approval of labels.
  • Reviews SPEC sheets, enter information in Disposition Log, file.
  • Assists QA with the tracking and/or completion of CAPAs and Customer Complaints.
  • Assists QA with the tracking and/or completion of NCRs, OOSs, TMPs.
  • Assigns part numbers.
  • Reviews, tracks, and files training forms. Ensures the training log is updated.
  • Reviews calibration/maintenance records, update tracking log, file.
  • Ensure the records are complete and stored in a manner where they are readily retrievable.
  • Participates during audits (FDA, ISO, vendor)
  • Assists Document Control, (assign CC and document numbers, assist in obtaining approvals, auditing external documents, etc.) when necessary.
  • Other duties and task as assigned.

Competencies

To perform the job successfully, an individual should demonstrate the following competencies:

Organizational Support - follows policies and procedures; completes administrative tasks correctly and on time; supports organization's goals and values.

Quality - Demonstrates accuracy and thoroughness; monitors own work to ensure quality.

Written Communication - writes clearly and informatively; able to read and interpret written information.

Qualifications

The requirements listed below are representative of the knowledge, skill, and/or ability required.

  • Bachelor's degree (B.A. or B.S.), or equivalent combination of education and experience.
  • Minimum of 2 years' experience in working in an FDA or ISO regulated environment or equivalent training.
  • Knowledge of ISO 13485, ISO 9001, and FDA QSR preferred

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