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

Omeros Corp.

Director, Quality Control

Seattle, WA · On-site

The Director, Quality Control will provide strategic leadership in managing a growing team of ... Experience in big pharma/biotech; experience in a startup biopharma company is desirable

Omeros

Director, Quality Control

Seattle, WA · On-site

The Director, Quality Control will provide strategic leadership in managing a growing team of ... Experience in big pharma/biotech; experience in a startup biopharma company is desirable

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Quality Control Pharma information

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How much do quality control pharma jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for quality control pharma in Seattle, WA is $23.86, according to ZipRecruiter salary data. Most workers in this role earn between $20.53 and $26.25 per hour, depending on experience, location, and employer.

What is quality control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

What are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

Is Quality Control Pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It requires attention to detail, knowledge of laboratory techniques, and often involves certifications such as GMP training. The role offers stable employment opportunities in the pharmaceutical industry with potential for career advancement.

What are popular job titles related to Quality Control Pharma jobs in Seattle, WA?

For Quality Control Pharma jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Quality Control Pharma jobs in Seattle, WA look for?

The top searched job categories for Quality Control Pharma jobs in Seattle, WA are:

Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma job openings in Seattle, WA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 13% Part Time, 5% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $49,631 per year, or $23.9 per hour.

Director, Quality Control

Omeros Corp.

Seattle, WA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 18 days ago

Key responsibilities

  • Lead Quality Control activities for clinical and commercial products, including management of in-process and release testing of GMP products

  • Manage QC staff including hiring, developing, evaluating, and goal setting

  • Oversee GMP clinical and commercial stability planning, data analysis, and expiry/shelf-life determination

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.
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About Omeros

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

201 - 500 Employees

Headquarters location

Seattle, WA, US

Year founded

1994

Social media

Twitter

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