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Qc Biotech Jobs (NOW HIRING)

Omeros Corp.

Director, Quality Control

Seattle, WA · On-site

Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ... Lead Quality Control (QC) activities for clinical and commercial products, including management of ...

Bruker Corporation

QC Inspector

Bothell, WA · On-site

$37K - $66K/yr

At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry. Qualifications Minimum Education: Bachelor's degree in a related ...

SaniSure LLC

Quality Control Inspector

Camarillo, CA · On-site

$22 - $24/hr

S. and Europe, we supply global pharmaceutical and biotech companies with the critical tools they ... Job Summary The Quality Control Inspector inspects materials, parts, and products at different ...

Eagle Labs, Inc

QC Microbiologist

Seminole, FL · On-site

$85K - $87K/yr

Quality Control Microbiology Supervisor Overview: Quality Control (QC) Microbiology Supervisor ... Minimum 5 years of hands-on experience in a cGMP pharmaceutical or biotech microbiology laboratory ...

American Society for Quality

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

... biotechnology and clinical systems, including point-of-care (POC) and in vitro diagnostic (IVD ... The Sr. Quality Control Manager will develop and execute comprehensive quality control strategies ...

BioLegend

Quality Control Supervisor

San Diego, CA · On-site

Bachelor's or Master's Degree in Biology, Immunology or a related Science field * 4 to 6 years of biotech industry experience related to Quality Control * 2 years of experience supervising or leading ...

Neogen

Lead QC Microbiologist

Lexington, KY · On-site

$25.25 - $33.25/hr

Bachelor's degree in Microbiology, Biology, Biotechnology, or a related scientific discipline required. * Five or more years of QC microbiology experience in a pharmaceutical, biotechnology, medical ...

Neogen Corporation

Lead QC Microbiologist

Lexington, KY · On-site

$25.25 - $33.25/hr

Bachelor's degree in Microbiology, Biology, Biotechnology, or a related scientific discipline required. * Five or more years of QC microbiology experience in a pharmaceutical, biotechnology, medical ...

Frontage Laboratories

QC Manager

Exton, PA · On-site

Quality Control (QC) Manager Department: Biomarker & Biologics Location: Exton, PA ( Onsite ... Bachelor's or Master's in Biology, Biochemistry, Immunology, Biotechnology, or related field.

AstraZeneca

Quality Control Manager

Bogart, GA · On-site

Microbiology experience in quality control within a biotech , pharmaceutical , or biopharmaceutical manufacturing environment is helpful. * Prior supervisory experience is preferred. Competencies

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Showing results 41-60

All JobsQc Biotech Jobs

Qc Biotech information

See salary details

$30.5K

$81.3K

$129.5K

How much do qc biotech jobs pay per year?

As of Aug 11, 2026, the average yearly pay for qc biotech in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a QC Biotech?

To thrive as a QC Biotech, you need a solid background in biology, chemistry, and laboratory techniques, usually supported by a degree in life sciences or a related field. Familiarity with analytical instruments such as HPLC, PCR, and ELISA, as well as GMP regulations and LIMS software, is typically required. Attention to detail, strong problem-solving abilities, and effective teamwork are crucial soft skills for this role. These skills and qualities ensure accurate testing, regulatory compliance, and the integrity of biotechnological products.

What is a QC Biotech?

A QC (Quality Control) Biotech professional is responsible for ensuring that biotechnology products, such as pharmaceuticals, vaccines, or biologics, meet strict quality and safety standards. They perform laboratory tests, analyze samples, and document results to ensure compliance with regulatory guidelines. QC Biotech professionals play a crucial role in maintaining the integrity of products before they reach the market, working closely with other departments to resolve any quality issues. Their work helps protect patient safety and supports the success of biotech companies.

What is the difference between Qc Biotech vs Qc Microbiologist?

AspectQc BiotechQc Microbiologist
Required CredentialsBachelor's in Biology, Biotechnology, or related field; GMP/GxP trainingBachelor's in Microbiology, Biology, or related; microbiology certifications
Work EnvironmentBiotech manufacturing labs, quality control departmentsMicrobiology labs, pharmaceutical or biotech settings
Employer & Industry UsageBiotech companies, pharmaceutical manufacturersPharmaceutical firms, biotech research labs
Common Search & ComparisonYesYes

While both Qc Biotech and Qc Microbiologist roles involve quality testing in biotech and pharmaceutical settings, Qc Biotech focuses on overall product quality, including assays and validation, whereas Qc Microbiologists specialize in microbiological testing and contamination control. The roles often overlap but differ in specific expertise and focus areas.

What are some common challenges faced by QC Biotech professionals and how can they be addressed?

QC Biotech professionals often encounter challenges such as adapting to rapidly changing regulatory standards, troubleshooting complex assay discrepancies, and maintaining precise documentation under tight deadlines. Addressing these challenges requires continuous learning, strong attention to detail, and effective collaboration with cross-functional teams like R&D and manufacturing. Leveraging robust Standard Operating Procedures and clear communication with colleagues can help ensure consistent results and regulatory compliance.
More about Qc Biotech jobs
What cities are hiring for Qc Biotech jobs? Cities with the most Qc Biotech job openings:
What are the most commonly searched types of Qc Biotech jobs? The most popular types of Qc Biotech jobs are:
What states have the most Qc Biotech jobs? States with the most job openings for Qc Biotech jobs include:
What job categories do people searching Qc Biotech jobs look for? The top searched job categories for Qc Biotech jobs are:
Qc Biotech jobs near you
Infographic showing various Qc Biotech job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 88% Full Time, 5% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 93% Physical, 4% Hybrid, and 3% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

Director, Quality Control

Omeros Corp.

Seattle, WA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 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.
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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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