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Biotech Associate Jobs in Seattle, WA (NOW HIRING)

GenScript/ProBio

Warehouse Specialist

Redmond, WA · On-site

$26 - $28/hr

About GenScript Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation ... Associate's degree or higher in Supply Chain or a related field preferred * Previous experience in ...

GenScript/ProBio

Warehouse Specialist

Redmond, WA · On-site

$26 - $28/hr

About GenScript Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation ... Associate's degree or higher in Supply Chain or a related field preferred * Previous experience in ...

Danaher

Associate Network Automation Engineer

Seattle, WA · On-site +1

$75K - $85K/yr

Our 60,000+ associates work across the globe at more than 15 unique businesses within life sciences, diagnostics, and biotechnology. Are you ready to accelerate your potential and make a real ...

Danaher

Associate Network Automation Engineer

Seattle, WA · On-site

$75K - $85K/yr

Our 60,000+ associates work across the globe at more than 15 unique businesses within life sciences, diagnostics, and biotechnology. Are you ready to accelerate your potential and make a real ...

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All JobsBiotech Associate JobsBiotech Associate Jobs in Seattle, WA

Biotech Associate information

See Seattle, WA salary details

$12

$22

$37

How much do biotech associate jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for biotech associate in Seattle, WA is $22.61, according to ZipRecruiter salary data. Most workers in this role earn between $16.97 and $23.51 per hour, depending on experience, location, and employer.

What is a biotech associate?

Biotech Associates are professionals who support scientific research, development, and production in biotechnology companies or laboratories. They typically assist in conducting experiments, analyzing data, preparing samples, and maintaining laboratory equipment. Their work helps develop new products or processes in areas like pharmaceuticals, agriculture, and environmental science. Biotech Associates often have a background in biology, chemistry, or related fields and work under the supervision of scientists or senior researchers.

What are the key skills and qualifications needed to thrive as a biotech associate?

To thrive as a Biotech Associate, you need a solid background in biology, chemistry, or a related field, usually supported by a bachelor's or master's degree. Familiarity with laboratory techniques, data analysis software, and compliance with regulatory standards like GLP or GMP is essential. Strong attention to detail, problem-solving abilities, and effective teamwork are standout soft skills in this position. These skills ensure accurate experimental results, regulatory compliance, and efficient collaboration in fast-paced research environments.

What are some typical challenges faced by biotech associates when working in a laboratory setting?

Biotech Associates often encounter challenges such as troubleshooting complex experiments, maintaining strict adherence to safety protocols, and managing multiple projects simultaneously. Working with sensitive biological materials requires attention to detail and the ability to quickly adapt to unexpected results or equipment malfunctions. Collaboration with scientists and cross-functional teams is frequent, so strong communication skills are essential to ensure experiments are aligned with broader research goals.

What is the difference between Biotech Associate vs Laboratory Technician?

AspectBiotech AssociateLaboratory Technician
Required CredentialsBachelor's degree in biology, biotech, or related field; some roles may require experienceAssociate's degree or relevant certification; less emphasis on advanced degrees
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsAcademic labs, industrial labs, healthcare facilities
Employer & Industry UsageBiotech firms, pharmaceutical companies, research institutionsHospitals, research labs, manufacturing plants
Common Search & ComparisonYesNo

The main difference between a Biotech Associate and a Laboratory Technician lies in their educational requirements and work scope. Biotech Associates typically hold a bachelor's degree and engage in research and development activities within biotech companies or research institutions. Laboratory Technicians often have an associate's degree and focus on routine lab tasks, testing, and sample processing. Both roles are essential in laboratory settings but differ in responsibilities and qualifications.

What are the most commonly searched types of Biotech jobs in Seattle, WA?

The most popular types of Biotech jobs in Seattle, WA are:

What are popular job titles related to Biotech Associate jobs in Seattle, WA?

For Biotech Associate jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Biotech Associate jobs in Seattle, WA look for?

The top searched job categories for Biotech Associate jobs in Seattle, WA are:

What cities near Seattle, WA are hiring for Biotech Associate jobs?

Cities near Seattle, WA with the most Biotech Associate job openings:

Biotech Associate jobs near you
Infographic showing various Biotech Associate job openings in Seattle, WA as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $47,030 per year, or $22.6 per hour.

Associate Director / Director, Supplier Quality and Audits

Immunome, Inc.

Bothell, WA • On-site

Full-time

Re-posted 9 days ago

Job description

Company Overview
Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.
Position Overview
The Director / Associate Director, Supplier Quality and Audits supports the Head of GMP Quality Compliance in building and continuously improving Immunome's Supplier Quality Compliance and Audit Program.
This role leads supplier audit management, vendor governance, compliance monitoring, risk management, quality agreements, CAPA management, and inspection readiness for GxP suppliers and service providers, including CDMOs, CROs, contract laboratories, consultants, and other outsourced partners. It ensures supplier compliance and audit processes are risk-based, inspection-ready, and aligned with regulatory requirements and Immunome's Quality Management System, while maintaining an effective audit program and governance of outsourced GxP activities.
As a virtual biotechnology company, Immunome retains ultimate responsibility for the quality and compliance of outsourced operations, and this role is a key partner in ensuring audit effectiveness, governance, and inspection readiness across the product lifecycle. This role partners closely with Quality Operations, which manages day-to-day supplier oversight, while this position provides independent compliance oversight through risk assessments, audits, governance, and remediation follow-up.
Responsibilities
  • Support development and continuous improvement of Immunome's GxP Supplier Quality and Vendor Management Program.
  • Lead supplier qualification, risk classification, onboarding, and ongoing monitoring of GxP vendors and service providers.
  • Maintain supplier quality records, risk evaluations, audit reports, and performance metrics.
  • Support quality oversight of CDMOs, CROs, labs, consultants, and other outsourced service providers.
  • Partner with stakeholders to clearly define and maintain vendor responsibilities and compliance expectations.
  • Lead negotiation and lifecycle management of quality agreements.
  • Plan and conduct supplier audits and follow-up, including responses, CAPAs, and effectiveness checks.
  • Support inspection readiness for outsourced GxP operations, including regulatory and internal audit preparation.
  • Monitor supplier quality performance, including deviations, CAPAs, complaints, audit findings, and service-level trends.
  • Identify, escalate, and support remediation of supplier quality and compliance risks.
  • Support cross-functional vendor governance meetings and document decisions, actions, and follow-up commitments.
  • Develop and maintain supplier quality procedures, Quality Agreement templates, and related trackers and tools aligned with Immunome's Quality Management System and regulatory expectations.
  • Support continuous improvement of supplier quality, oversight, audit effectiveness, and inspection readiness.

Qualifications
  • Bachelor's degree in a scientific, technical, or related field; advanced degree preferred.
  • 8+ years of biopharmaceutical industry experience, including direct oversight of third parties performing GxP activities, cGMP manufacturing, testing, or clinical operations, or equivalent experience.
  • Demonstrated experience performing and managing supplier qualification and supplier audit programs.
  • Experience supporting virtual, outsourced, or external manufacturing and service provider models preferred.
  • Ability to travel domestically and internationally up to 20%, with occasional evening/weekend commitment to support audits and inspections.
  • Professional certifications (e.g., ASQ CQA, CMQ/OE, RQAP, ISO 9001/13485 Lead Auditor, RAC) or equivalent quality/auditing/regulatory certifications are highly desirable.

Knowledge and Skills
  • Strong knowledge of Supplier Quality Management, GxP auditing, Quality Systems, and regulatory compliance within the biotechnology or pharmaceutical industry.
  • Experience managing supplier qualification, governance, quality agreements, risk assessments, and oversight of CDMOs, CROs, labs, and other GxP service providers.
  • Demonstrated experience conducting supplier audits, managing audit programs, supporting regulatory inspections, CAPA management, and inspection readiness activities.
  • Proven Lead Auditor experience with strong knowledge of FDA, EU, ICH, and applicable GxP regulations.
  • Strong understanding of cGMP manufacturing, quality assurance/control, validation, and outsourced pharmaceutical operations.
  • Experience developing audit schedules, audit plans, audit reports, and auditor training programs.
  • Excellent organizational, communication, collaboration, negotiation, analytical, and problem-solving skills.
  • Ability to manage multiple priorities in a fast-paced environment and adapt effectively to changing business needs.

Washington State Pay Range
$175,100-$239,998 USD
E/E/O
Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
E-Verify
Immunome, Inc. is a participant in E-Verify. Please review the following notices: E-Verify Participation Poster | Right to Work Poster (English) | Right to Work Poster (Spanish).

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