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

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

Quality Engineer II

Bothell, WA · On-site

$82K - $138K/yr

With our company's history spanning over 40 years, you will have stability, career growth ... Support Change Control Board function through a technical and procedural review of engineering ...

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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 Aug 28, 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 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.

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 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.

Is quality control stability a good career choice?

Quality Control Stability is a role focused on maintaining product consistency and compliance through testing and monitoring processes. It often requires attention to detail, knowledge of industry standards, and proficiency with testing tools or software. This career can offer steady employment opportunities in manufacturing, pharmaceuticals, or food industries, with potential for advancement and certification.

Is quality control stability a good career path?

Quality control stability involves ensuring products meet quality standards over time, often requiring attention to detail and knowledge of testing procedures. It can offer steady employment and opportunities for advancement in manufacturing, pharmaceuticals, or food industries, especially for those with relevant certifications or experience. The career can be stable, but growth depends on industry demand and individual skill development.

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:

Director, Quality Control

Omeros Corp.

Seattle, WA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 days ago


Job description


We are a fast-growing and dynamic organization seeking a Director, Quality Control to join our CMC team. The Director, Quality Control will provide strategic leadership in managing a growing team of scientists responsible for QC-related activities and operations. This individual will be responsible for providing scientific leadership, defining QC strategy and determining a roadmap for QC related activities and operations to meet corporate objectives. The scope of this role covers all phases of product development (clinical and commercial) at Omeros for both large and small pharmaceutical products.
Good things are happening at Omeros!
Who is Omeros?
Omeros is an innovative biotechnology company that discovers, develops, and commercializes first-in-class small-molecule and protein therapeutics for large-market and orphan indications, with particular emphasis on complement-mediated diseases, cancers, and addictive or compulsive disorders. Omeros' lead lectin pathway inhibitor YARTEMLEA®, which inhibits the pathway's effector enzyme MASP-2, is FDA-approved for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA) in adult and pediatric patients ages two years and older, with a planned U.S. launch in January 2026. A marketing authorization application for YARTEMLEA in TA-TMA is currently under review by the European Medicines Agency, with a decision expected in mid-2026. OMS1029, Omeros' long-acting MASP-2 inhibitor, has successfully completed Phase 1 clinical trials.
Under a recently announced asset purchase and licensing agreement, Novo Nordisk acquired global rights to zaltenibart (formerly OMS906), a MASP-3 inhibitor in clinical development for PNH and other alternative pathway indications, along with associated intellectual property and related assets. Omeros' pipeline also includes OMS527, a phosphodiesterase 7 inhibitor in clinical development for cocaine use disorder and fully funded by the National Institute on Drug Abuse, as well as a growing portfolio of novel molecular and cellular oncology programs. For more information about Omeros and its programs, visit www.omeros.com.
What are your job responsibilities?
  • Lead Quality Control (QC) activities for clinical and commercial products, including management of in-process and release testing of GMP products
  • Lead and manage QC staff including hiring, developing, evaluating and goal setting
  • 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 requirements for compliance with cGMP regulations at external contract manufacturing and testing organizations
  • Oversee product release and stability specification setting and COA generation
  • Oversee and approve release of QC components of GMP manufacturing batch and test records at external contract organizations
  • Develop Quality Control strategy and direction in conjunction with the development of analytical methods and manufacturing processes by the Omeros Technical CMC teams
  • Partner with internal and external stakeholders to transfer, qualify and validate analytical methods
  • Establish and maintain quality control standards applicable to the clinical and commercial product phases
  • Author/review relevant sections of regulatory filing reports and submissions
  • Drive continuous improvement projects in collaboration with internal and external stakeholders

What education and experience do you need?
  • PhD in Analytical Chemistry, Biochemistry, Biology or a related scientific field
  • 10+ years Quality Control experience is required, preferably with both biologics and small molecules
  • Strong knowledge of GMPs, ICH guidelines and Quality management systems
  • Experience with analytical methods technology transfer to third parties
  • Experience with regulatory authority meetings and GMP site inspections
  • Extensive experience with analytical method development and validation
  • Expertise with stability testing, data trending and expiry setting strategy
  • Experience with testing injectable and oral dosage forms preferred
  • Experience in big pharma/biotech; experience in a startup biopharma company is desirable
  • Proficiency in MS Office, Word and Excel; statistical analysis software is desirable

Behavioral Competencies Required:
  • Demonstrated ability to build and maintain positive and collaborative relationships with management, peers, subordinates, and externally with third party contract organizations
  • Excellent written and oral communication skills with a proven track record of developing employees
  • Self-motivated and detail-oriented, with the highest integrity

Other Responsibilities:
  • Occasionally required to travel
  • Ability to travel 10% of the time

Supervisory Responsibilities:
  • Management and supervision of a small team and contractor(s)
  • Responsibilities may include interviewing, hiring and training employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems

Compensation and Benefits:
Omeros is proud to offer a competitive total compensation package designed to support the lives of our employees and their families. The wage scale for Director Quality Control position is ($210,000-$245,000). Salaries will be determined based on knowledge, skills, education, and experience relevant to the role. Employees are offered medical, dental, vision, life insurance, and a 401(k) plan with a company match. Employees accrue three weeks of vacation and 80 hours of sick time on an annual basis and receive twelve paid holidays throughout the calendar year. This position is eligible for incentive and stock options. To learn more about Omeros, please visit www.omeros.com.
Omeros is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to status as a protected veteran or a qualified individual with a disability, or other protected status such as race, religion, color, national origin, sex, age, marital status, or any other factor determined to be unlawful by federal, state, or local statutes.
It is our policy to provide reasonable accommodation to anyone with a disability who needs assistance completing the job application process. If you need assistance, you can either send an e-mail to hr@omeros.com or contact Omeros, asking for Human Resources, at (206) 676-5000.

Omeros logo

About Omeros

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

201 - 500 Employees

Headquarters location

Seattle, WA, US

Year founded

1994

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