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Quality Control Stability Jobs in Seattle, WA (NOW HIRING)

Omeros

Director, Quality Control

Seattle, WA

Oversee GMP clinical and commercial stability planning, execution, statistical data analysis and data trending in support of product expiry/shelf-life determination * Oversee Quality Control ...

Omeros Corp.

Director, Quality Control

Seattle, WA · On-site

Oversee GMP clinical and commercial stability planning, execution, statistical data analysis and data trending in support of product expiry/shelf-life determination * Oversee Quality Control ...

nathr

Quality Control Supervisor

Monroe, WA

$32.08 - $38.81/hr

Quality Control (QC) Supervisor Pay: $32.08 - $38.81/hour Schedule: Monday to Friday 8:00am-4:30pm ... If you're looking for stability, great benefits, and a positive work environment, this is the place ...

nathr

Quality Control Supervisor

Monroe, WA

$32.08 - $38.81/hr

Quality Control (QC) Supervisor Pay: $32.08 - $38.81/hour Schedule: Monday to Friday 8:00am-4:30pm ... If you're looking for stability, great benefits, and a positive work environment, this is the place ...

nathr

Quality Control Supervisor

Monroe, WA · On-site

$32.08 - $38.81/hr

Quality Control (QC) Supervisor Pay: $32.08 - $38.81/hour Schedule: Monday to Friday 8:00am-4:30pm ... If you're looking for stability, great benefits, and a positive work environment, this is the place ...

Peregrine Team

Quality Control Analyst

Seattle, WA · On-site

$27.25 - $36.75/hr

Peregrine Team is hiring a Quality Control Analyst to support laboratory testing and ensure product ... Support investigations and deviations * Assist with stability studies and data analysis ...

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All JobsQuality Control Stability JobsQuality Control Stability Jobs in Seattle, WA

Quality Control Stability information

See Seattle, WA salary details

$34.7K

$92.5K

$147.4K

How much do quality control stability jobs pay per year?

As of Jul 18, 2026, the average yearly pay for quality control stability in Seattle, WA is $92,548.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,800.00 and $113,800.00 per year, depending on experience, location, and employer.

What career paths are possible in QC?

Career paths in Quality Control (QC) include roles such as QC Technician, QC Analyst, Quality Assurance Specialist, and Quality Manager. Advancement often involves gaining experience, certifications like ASQ certifications, and developing skills in inspection, testing, and data analysis within manufacturing, pharmaceuticals, or food industries.

What is the difference between Quality Control Stability vs Quality Control Inspector?

AspectQuality Control StabilityQuality Control Inspector
CertificationsOften requires certifications like Six Sigma, ISO auditor, or quality management certificationsTypically requires quality inspection certifications or training
Work EnvironmentFocuses on maintaining process stability in manufacturing or production settingsPerforms inspections on products or materials on the production line
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and industries emphasizing process consistencyCommon in manufacturing, food production, and assembly lines

Quality Control Stability involves ensuring that manufacturing processes remain consistent over time, emphasizing process control and reduction of variability. In contrast, a Quality Control Inspector primarily conducts inspections to verify product quality at various stages. Both roles are essential in quality management but focus on different aspects of quality assurance.

Which pays more, QA or QC?

In the field of Quality Control Stability, Quality Assurance (QA) roles generally offer higher salaries than Quality Control (QC) positions due to their broader responsibilities and focus on process improvement. QA jobs often require more experience and may involve certifications like Six Sigma or ISO standards, which can also influence pay. However, salaries vary based on industry, location, and level of experience.

What are some common challenges faced in a Quality Control Stability role, and how can they be addressed?

Professionals in Quality Control Stability often encounter challenges such as managing tight timelines for stability testing, interpreting ambiguous results, and ensuring compliance with evolving regulatory requirements. Effective communication with cross-functional teams—such as R&D, production, and regulatory affairs—is essential to address discrepancies and maintain data integrity. Staying organized, maintaining thorough documentation, and keeping up to date with industry guidelines help mitigate these challenges and ensure smooth workflow.

What are the key skills and qualifications needed to thrive as a Quality Control Stability specialist, and why are they important?

To thrive as a Quality Control Stability specialist, you need a solid background in chemistry or related sciences, experience with stability testing, and typically a bachelor’s degree in a scientific field. Familiarity with laboratory instruments (such as HPLC, GC), stability management systems, and knowledge of regulatory guidelines like ICH are essential. Attention to detail, problem-solving, and strong organizational skills help ensure accurate data analysis and effective reporting. These abilities are crucial for maintaining compliance, product safety, and reliability in pharmaceutical or biotech environments.

What is a Quality Control Stability role?

A Quality Control Stability role involves monitoring and evaluating the stability of pharmaceutical products, ensuring they maintain their quality, safety, and efficacy throughout their shelf life. Professionals in this position design and execute stability studies, analyze the results, and document findings according to regulatory requirements. They play a crucial part in ensuring compliance with industry standards and supporting product development and release. This role typically requires expertise in analytical testing, regulatory guidelines, and laboratory practices.

Is QC analyst a stressful job?

A QC analyst role involves inspecting and testing products to ensure quality standards are met, which can be demanding during tight deadlines or when addressing product issues. The job often requires attention to detail, adherence to safety protocols, and sometimes working in environments with strict regulatory requirements, which can contribute to stress levels.

What is quality control salary?

The salary for a quality control stability role typically ranges from $40,000 to $70,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced professionals with certifications can earn higher wages. Salaries often include benefits such as health insurance and paid time off.
What are the most commonly searched types of Quality Control Stability jobs in Seattle, WA? The most popular types of Quality Control Stability jobs in Seattle, WA are:
What are popular job titles related to Quality Control Stability jobs in Seattle, WA? For Quality Control Stability jobs in Seattle, WA, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability jobs in Seattle, WA look for? The top searched job categories for Quality Control Stability jobs in Seattle, WA are:
Quality Control Stability jobs near you
Principal, Quality Control

Principal, Quality Control

Lyell Immunopharma

Bothell, WA • On-site

Full-time

Re-posted 2 days ago

Job description

The Principal, Quality Control is responsible for providing subject matter expertise (SME) in analytical method qualification, validation, and regulatory submission authoring for cell therapy products. This role partners closely with Analytical Development, Manufacturing, MSAT, Process Development, Regulatory, and Quality Assurance to support technology transfer, method validation, and commercialization efforts including preparation for Biologics License Application (BLA) submission(s).
The incumbent will serve as a Quality Control representative on cross-functional project teams, ensuring that product-related activities are executed in compliance with GMP requirements while supporting timelines for clinical and commercial milestones.
The Principal, QC will provide scientific and strategic guidance and leadership for method validation programs, including the design, execution, and documentation of validation activities for cell-based, flow cytometry-based, and PCR-based release and stability assays. This role requires expertise in authoring CMC quality sections for IND and BLA regulatory submissions and serves as a key QC interface with Regulatory Affairs, QA, and Manufacturing during inspections and agency interactions.
KEY ROLES AND RESPONSIBILITIES:
  • Serve as the QC analytical SME for the design, development, and validation strategy for cell therapy release and stability methods, including cell-based potency assays, flow cytometry-based phenotyping, and PCR-based methods (e.g., VCN, residual plasmid).
  • Provide technical oversight for method transfers from Analytical Development or external labs, ensuring scientific rigor and regulatory acceptability.
  • Lead method qualification or validation strategy in alignment with ICH Q2(R1)/Q2(R2), ICH Q6B.
  • Evaluate method performance data critically; provide scientific justification for acceptance criteria, method parameters, and specification setting.
  • Serve as QC SME during regulatory agency inspections, partner audits, and internal GMP audits related to analytical methods and testing strategies.
  • Author CMC quality sections for IND and BLA submissions, including analytical method descriptions, method validation summaries, specification justifications, and stability program summaries (Module 3).
  • Contribute to authoring Contamination Control Strategy (CCS) sections in regulatory filings, in alignment with current regulatory expectations.
  • Act as the Quality Control representative on cross-functional project teams supporting product development, tech transfer, method validation, and commercialization activities.
  • Serve as Quality Control Subject Matter Expert (SME) for BLA coordination activities.
  • Drive continuous improvement initiatives within the QC laboratory, including method lifecycle management, assay robustness improvements, and test efficiency optimization.
  • Participate in cross-functional readiness activities to ensure the QC department is prepared for regulatory inspections as applicable.
  • Initiate, lead, and contribute to deviations, Change Controls, and CAPAs associated with QC methods, analytical instrumentation, and release testing. Experience with MasterControl is a plus.
KNOWLEDGE, SKILLS AND ABILITIES:
  • Expertise in cell therapy QC analytical methods, including flow cytometry, PCR-based assays, and cell-based functional/potency assays.
  • Comprehensive knowledge of ICH guidelines applicable to QC, including ICH Q2(R1)/Q2(R2), ICH Q6B, ICH Q1E, ICH Q9, and ICH Q14.
  • Proven capability to design and oversee execution of qualification/validation protocols.
  • Strong working knowledge of GMP-regulated laboratory operations, GDP principles, and LIMS systems.
  • Ability to work effectively both independently and cross-functionally with Analytical Development, Manufacturing, MSAT, Regulatory, Supply Chain, and external partners to set goals, develop sound project plans, monitor progress, and report results.
  • Outstanding communication, emotional intelligence and interpersonal skills.
  • Curious and proactive mindset with a continuous improvement orientation; actively seeks to understand processes, identify risks, and implement sustainable quality solutions.
  • Fast learner, adaptable, and has the desire and ability to work in a fast-paced, start-up environment.
  • Excellent analytical skills and scientific/technical expertise.
PREFERRED EDUCATION:
  • or MSc. in Biology, Immunology, Cell Biology, Biochemistry, Molecular Biology, or a related life sciences field with a minimum of 15 years' experience; or
PREFERRED EXPERIENCE:
  • 10-15 years of experience in GMP biopharmaceutical operations including 4 years in cell therapy and/or lentiviral manufacturing operations.
  • Minimum of 5+ years in Quality Control
  • Direct experience supporting BLA submissions, regulatory filings, and/or health authority inspections.
  • Experience in commercial manufacturing and post-approval lifecycle management.
  • Familiarity with contamination control principles, including Disinfection Studies, Environmental Monitoring Program and aseptic process simulation.

WEEKEND WORK AND HOLIDAY COVERAGE:
Due to the nature of our autologous cell therapies and the need to deliver life-saving treatments to our patients as timely as possible, weekend work, and holiday work will occasionally be required. We are looking for passionate team members to join our team that are willing to learn, grow, and evolve with us. Part of this evolution will be to work together to continually assess and modify our shift structure to best support delivering these critical products to our patients.
The salary range for this position is between $148,000 - $185,000, annually, with the opportunity to earn an annual bonus. The salary range is an estimate, and the actual salary may vary based on Lyell's compensation practices and an applicant's qualifications and experience. Employees are also eligible to participate in Lyell's Equity Incentive Plan.
At Lyell, we believe that highest performing teams include people from a wide variety of backgrounds and experiences who respectfully challenge each other. We are committed to building an open, diverse and inclusive culture for all employees. Lyell is proud to be an equal opportunity employer and does not discriminate on the basis of race, color, citizenship status, national origin, ancestry, sex, sexual orientation, age, religion, creed, physical or mental disability, medical condition, marital status, veteran status or any other characteristics protected under applicable federal, state and local laws.
We've learned from experience that some of the best people don't always match our requirements perfectly - if you're interested and think you could fit, please don't hesitate to apply.

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