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Analytical Development Jobs in Seattle, WA (NOW HIRING)

City of Kent, WA

Training Development Analyst

Kent, WA · On-site

$8.0K - $9.7K/mo

The City of Kent is seeking a proactive and detail-oriented Training Development Analyst to lead city-wide training initiatives that support employee growth, legal compliance, and organizational ...

Collabera

SDET/ Automation Engineer

Bellevue, WA

As a result of these efforts, we have been recognized by Staffing Industry Analysts (SIA) as the ... Job Title: SDET/ Automation Engineer Location: Madison, WI or Bellevue, WA Duration: 6 Months ...

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Analytical Development information

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$42.7K

$85.3K

$126.9K

How much do analytical development jobs pay per year?

As of Aug 6, 2026, the average yearly pay for analytical development in Seattle, WA is $85,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,300.00 and $105,800.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Analytical Development?

To thrive in Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a relevant degree and experience in analytical methodologies. Familiarity with laboratory instruments such as HPLC, GC, and mass spectrometry, as well as knowledge of regulatory guidelines like ICH and GMP, is essential. Strong problem-solving skills, attention to detail, and effective communication set standout professionals apart in this role. These skills ensure the accurate development, validation, and transfer of analytical methods critical for product quality and regulatory compliance.

What is analytical development?

Analytical development is a field within pharmaceutical and biotech industries focused on creating and validating methods to analyze the quality, purity, and potency of drug substances and products. It involves developing techniques such as chromatography and spectroscopy, often requiring knowledge of regulatory standards like GMP and validation processes. Professionals in this area support drug development by ensuring analytical methods are reliable and compliant with industry regulations.

What is the job description of analytical development?

Analytical development involves designing, optimizing, and validating analytical methods to measure the quality and stability of pharmaceutical products. Professionals in this field use techniques such as chromatography and spectroscopy, often working in laboratories under Good Laboratory Practice (GLP) standards. The role requires strong attention to detail, scientific knowledge, and proficiency with laboratory instruments and regulatory guidelines.

What are some common challenges faced in an Analytical Development role, and how can job seekers prepare for them?

Professionals in Analytical Development often encounter challenges such as developing robust methods for complex samples, meeting tight project deadlines, and ensuring regulatory compliance. To prepare, job seekers should build strong problem-solving skills, gain familiarity with a range of analytical techniques (such as HPLC, GC, and spectroscopy), and stay current with industry regulations like ICH guidelines. Collaborating effectively with cross-functional teams, such as Quality Control and Research & Development, is also essential for success in this role.

What is the difference between Analytical Development vs Quality Control Analyst?

AspectAnalytical DevelopmentQuality Control Analyst
Primary FocusDeveloping and optimizing analytical methods for new productsPerforming routine testing to ensure product quality
Work EnvironmentLaboratories involved in method development and validationQuality control labs conducting batch testing and release
Required CredentialsBachelor's or higher in Chemistry, Biochemistry, or related fields; experience in method developmentBachelor's in Chemistry, Biology, or related fields; experience in testing procedures

Analytical Development professionals focus on creating and refining analytical methods for new products, while Quality Control Analysts perform routine testing to verify product quality. Both roles require similar educational backgrounds and work in laboratory settings, but their responsibilities differ in scope and purpose.

What are the most commonly searched types of Analytical Development jobs in Seattle, WA? The most popular types of Analytical Development jobs in Seattle, WA are:
What are popular job titles related to Analytical Development jobs in Seattle, WA? For Analytical Development jobs in Seattle, WA, the most frequently searched job titles are:
What job categories do people searching Analytical Development jobs in Seattle, WA look for? The top searched job categories for Analytical Development jobs in Seattle, WA are:
Analytical Development jobs near you
Infographic showing various Analytical Development job openings in Seattle, WA as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $85,336 per year, or $41 per hour.

Associate Director, Quality Control, Biologics

Immunome, Inc.

Bothell, WA • On-site

Full-time

Re-posted 6 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 submitted to the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-3050, an IND-cleared FAP-targeted radiotherapy; and IM-1617, an IND-cleared solid tumor ADC. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.
Position Overview
Immunome is seeking a highly experienced and strategic Associate Director, Quality Control, Biologics to lead QC strategy and execution in support of our biologics and ADC portfolio. This role will be responsible for oversight of GMP QC activities, including analytical method transfer, qualification and validation, release and stability testing, investigation support, external testing lab management, and QC documentation supporting clinical development and regulatory submissions.
The successful candidate will bring deep technical expertise in biologics and ADC analytical testing, a strong working knowledge of GMP requirements and global regulatory expectations, and the leadership skills necessary to manage cross-functional and external partners. This position offers a highly visible opportunity to build scalable QC processes and ensure Immunome's products are tested with scientific rigor, operational discipline, and patient-centered quality.
Responsibilities
QC Strategy and Governance
  • Develop and implement phase-appropriate QC strategies for biologics and ADC programs across drug substance and drug product development, release, and stability.
  • Provide scientific, technical, and GMP oversight for QC testing, method lifecycle activities, specifications, reference standards and critical reagent strategies.
  • Contribute to the long-term vision for Immunome's QC capabilities, including evaluation of technologies, systems, and external partnerships to support portfolio growth.

Program Oversight and Execution
  • Oversee execution of GMP and non-GMP analytical testing for intermediates, drug substance, drug product, and stability samples in collaboration with CTLs and CDMOs.
  • Lead review and interpretation of QC data, trends, OOS/OOT results, deviations, investigations, CAPAs, change controls, and technical reports.
  • Serve as the QC representative on cross-functional program teams, ensuring QC deliverables are aligned with CMC timelines.

External Laboratory and Partner Management
  • Manage external contract testing laboratories and CDMO QC functions to ensure timely, compliant, and high-quality study execution.
  • Oversee method transfer, qualification, validation, verification, and troubleshooting activities across external laboratories.
  • Establish expectations for documentation quality, sample management, stability pulls, and communication cadence with external partners.

Regulatory and Documentation Support
  • Author and review QC-related SOPs, protocols, validation and qualification plans, method transfer reports, specifications, CoAs, stability summaries, and regulatory submission content.
  • Support preparation of IND, BLA, CTD, and other global regulatory submissions, including responses to health authority questions related to QC and analytical controls.
  • Stay informed of emerging regulatory expectations and compendial requirements, integrating relevant guidance into Immunome's QC strategy.

Leadership and Collaboration
  • Lead, mentor, and develop scientists and technical staff, fostering a high-performance culture grounded in quality, accountability, and collaboration.
  • Partner closely with Analytical Development, Process Development, Manufacturing, Quality Assurance, Regulatory CMC, Supply Chain, and Program Management to align QC plans with broader development objectives.
  • Communicate complex QC data, risks, and recommendations clearly to functional leaders and program teams, enabling timely, science-based decision-making.

Qualifications
  • A Bachelor's or advanced degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, or a related field.
  • 10+ years of experience in Quality Control, Analytical Development, CMC, or related functions within the biotechnology or biopharmaceutical industry or equivalent; advanced degree may offset some experience.
  • Demonstrated experience supporting QC programs for biologics; ADC experience strongly preferred.
  • Proven experience with GMP release and stability testing, analytical method transfer, qualification, validation, and lifecycle management.
  • Prior experience managing CTLs, CDMOs, CROs, or other external partners supporting regulated testing.
  • Experience managing matrixed projects, or external partner relationships in a fast-paced development environment.

Knowledge and Skills
  • In-depth understanding of GMP standards, data integrity expectations, and global regulatory guidance relevant to biologics QC, analytical validation, stability, and CMC submissions.
  • Strong technical knowledge of biologics and ADC product quality attributes, including potency, purity/impurities, charge variants, glycosylation, aggregation, conjugation-related attributes, and linker-payload characteristics.
  • Working knowledge of analytical technologies such as HPLC/UPLC, CE-SDS/cIEF, icIEF, LC-MS, ELISA, binding and potency assays, compendial methods, and microbiological testing.
  • Operational and strategic experience with phase-appropriate method development, qualification, validation, method transfer, compendial verification, and stability program design.
  • Ability to assess QC data trends, deviations, OOS/OOT results, and analytical risks, translating findings into practical recommendations and CAPA plans.
  • Excellent judgment and the ability to transition seamlessly between hands-on technical review and strategic decision-making.
  • Comfortable with ambiguity and complex challenges; adapt quickly and lead teams through dynamic environments.
  • Exceptional communication skills with the ability to collaborate effectively across functions and with external partners.
  • Solution-oriented problem-solving skills, with the capacity to manage multiple projects and prioritize in a fast-paced setting.

Washington State Pay Range
$177,813-$203,985 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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