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Quality Control Biotechnology Jobs in Washington

Precigen, Inc

QC Manager

Germantown, MD · On-site

$95K - $120K/yr

... and biotech industry under GMP guidelines, with demonstrated expertise in multiple disciplines and assays. * 2+ years of supervisory experience. * Advanced experience with QC testing in ...

Granules

Quality Control Manager

Chantilly, VA · On-site

$100K - $120K/yr

Requires minimum BA/BS in Biochemistry, Chemistry or related field with 10-15 years' experience in the biotech or pharmaceutical industry. Management experience in Quality Control required MS/MA.

Granules

Biochemist I/II (QC Analyst)

Chantilly, VA · On-site

$55K - $80K/yr

The role of Biochemist I/II (QC Analyst) is responsible for supporting the operations and ... or Biotechnology or related field. * Minimum 2 - 5 years of experience in using analytical ...

Quality Agents

Process Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology ... Collaborate cross-functionally with QA, QC, Manufacturing, and Engineering teams. Support ...

Quality Agents, LLC

Process Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology ... Collaborate cross-functionally with QA, QC, Manufacturing, and Engineering teams. Support ...

Quality Agents, LLC

Process Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology ... , QC, Manufacturing, and Engineering teams. • Support commissioning, qualification (IQ/OQ/PQ ...

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Quality Control Biotechnology information

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$33

How much do quality control biotechnology jobs pay per hour?

As of Jul 30, 2026, the average hourly pay for quality control biotechnology in Washington is $23.75, according to ZipRecruiter salary data. Most workers in this role earn between $20.43 and $26.15 per hour, depending on experience, location, and employer.

What are typical challenges faced by professionals in Quality Control Biotechnology, and how can they be addressed?

Professionals in Quality Control Biotechnology often encounter challenges such as maintaining compliance with stringent regulatory standards, managing tight deadlines for product release, and adapting to rapidly evolving technologies. To address these issues, staying updated on regulatory changes, implementing robust documentation practices, and participating in ongoing training are essential. Collaboration with cross-functional teams, such as Research & Development and Manufacturing, also helps ensure that quality standards are integrated throughout the production process.

What are the key skills and qualifications needed to thrive as a Quality Control professional in Biotechnology, and why are they important?

To thrive as a Quality Control professional in Biotechnology, you need a solid background in biology or chemistry, attention to detail, and knowledge of regulatory standards, often supported by a relevant degree. Familiarity with laboratory equipment, analytical techniques (like HPLC, PCR), and quality management systems such as GMP or ISO 9001 is typically required. Strong problem-solving skills, teamwork, and clear communication help you excel in ensuring product integrity and compliance. These skills are crucial for maintaining high product standards, meeting regulatory requirements, and ensuring the safety and efficacy of biotechnological products.

What are Quality Control Biotechnology jobs?

Quality Control Biotechnology jobs involve ensuring that biotechnological products, such as pharmaceuticals, vaccines, or laboratory reagents, meet required quality and safety standards. Professionals in this field design and perform tests, analyze data, and document results to verify that products comply with regulatory guidelines. They often work in laboratories, using specialized equipment to detect contaminants or inconsistencies. These roles are crucial for maintaining product integrity and protecting public health.

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

AspectQuality Control BiotechnologyQuality Assurance Biotechnology
Primary FocusTesting and inspecting biotech products to ensure they meet standardsDeveloping and implementing processes to prevent defects and ensure quality
Work EnvironmentLaboratories, testing facilitiesOffice settings, compliance departments
CertificationsGMP, GLP, laboratory certificationsGMP, ISO, audit-related certifications

While both roles aim to ensure biotech product quality, Quality Control Biotechnology focuses on testing and inspection, whereas Quality Assurance Biotechnology emphasizes process development and compliance to prevent issues. Both are essential for product integrity in the biotech industry.

What are popular job titles related to Quality Control Biotechnology jobs in Washington? For Quality Control Biotechnology jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Quality Control Biotechnology jobs in Washington look for? The top searched job categories for Quality Control Biotechnology jobs in Washington are:
What cities in Washington are hiring for Quality Control Biotechnology jobs? Cities in Washington with the most Quality Control Biotechnology job openings:
Quality Control Biotechnology jobs near you
Infographic showing various Quality Control Biotechnology job openings in Washington as of July 2026, with employment types broken down into 2% Locum Tenens, 4% Internship, 76% Full Time, 15% Part Time, 2% Contract, and 1% Summer. Highlights an 73% Physical, 5% Hybrid, and 22% Remote job distribution, with an average salary of $49,395 per year, or $23.7 per hour.

QC Manager

Precigen, Inc

Germantown, MD • On-site

$95K - $120K/yr

Full-time

Re-posted 16 days ago

Job description

Job Title: QC Manager

Department: Quality Control - Analytical

GENERAL DESCRIPTION:

  • QC Manger is responsible for overseeing a team of QC Analysts and is also responsible for maintaining the QC Laboratory in a state of cGMP compliance.

    DUTIES AND RESPONSIBILITIES:
  • Training, coaching, and development of QC staff
  • Develop, revise, and review SOPs, qualification/validation protocols and reports.
  • Write deviations, CAPA’s and own change controls.
  • Review/Provide guidance for deviations/CAPA’s generated by QC Analysts
  • Responsible for reviewing invalid assays and lead invalid assay investigations
  • Participating in OOS investigations
  • Responsible for ensuring all analytical data generated by QC lab to be initiated on time and completed within established TAT’s.
  • Perform review of QC documentation (equipment logbooks, sol’n prep record, cell line records, TRF’s, etc)
  • Ensure test results are entered into the appropriate reports
  • Track/Trend Ref. Std, Assay Control and Critical Reagents
  • Track equipment cleaning/PM/Calibration schedules
  • Review equipment IOQ’s and Re-Qualifications
  • QC Process/Procedure continuous improvements
  • Perform other duties as needed

EDUCATION AND EXPERIENCE:

  • BS degree in the Biological Sciences, Bioengineering, or Chemistry.
  • 7+ years of experience performing QC activities in the pharmaceutical and biotech industry under GMP guidelines, with demonstrated expertise in multiple disciplines and assays.
  • 2+ years of supervisory experience.
  • Advanced experience with QC testing in pharmaceutical or biopharmaceutical laboratories
  • Familiarity with analytical testing procedures: qPCR, HPLC, ELISA, Cell-based Assays, etc.


DESIRED KEY COMPETENCIES:

  • Demonstrated ability to manage a team and work independently on projects, and review project data and provide summary analysis reports based upon the data
  • Ability to provide support for regulatory and client audits, as well as interact with clients.
  • Ability to effectively negotiate and build collaboration amongst individuals.
  • Ability to be self-motivated, proactive, accountable, and flexible
  • Demonstrate the ability to develop, coach and mentor key employees.
  • Excellent interpersonal, verbal, and written communication skills are essential in this collaborative work environment.
  • High attention to detail, highly organized, and excellent documentation skills
  • Strong scientific, analytical, and problem-solving skills as well as sound judgment, to identify problems and leads efforts to resolve them
  • Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based on upon changing priorities.