Director, Quality Control

We are a fast-growing and dynamic organization seeking aDirector Quality Controlto 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!

Come join our Marketing Team!

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 pathways 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 inJanuary 2026. A marketing authorization application for YARTEMLEA in TA-TMA is currently under review by theEuropean 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 agreementNovo Nordiskacquired 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 theNational 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.

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($210000-$245000). 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.

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@ or contact Omeros asking for Human Resources at .