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Biotech Quality Control Jobs in Washington, DC (NOW HIRING)

Precigen, Inc

Manager, Quality Control

Germantown, MD · On-site

$105K - $140K/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 ...

Pharmaron

Quality Control Data Reviewer I

Germantown, MD · On-site

$68K - $75K/yr

Quality Control Data Reviewer I Salary Range : $68,000- 75,000 Location : Germantown, MD About ... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ...

Pharmaron

Quality Control Data Reviewer I

Germantown, MD · On-site

$68K - $75K/yr

Quality Control Data Reviewer I Salary Range : $68,000- 75,000 Location : Germantown, MD About ... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ...

ATCC Biotechnology

Senior Director, Quality

Manassas, VA · On-site

$120 - $160/hr

Oversee QC laboratory operations, including method validation and release testing, ensuring consistent product disposition decisions and compliance with applicable standards. * Validation & Data ...

PSG Global Solutions

Quality Analyst

Gaithersburg, MD · On-site

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not ... Participate in QC project teams to accomplish effective results. * Check expiration dates for media ...

PSG Global Solutions

Quality Analyst

Gaithersburg, MD · On-site

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not ... Participate in QC project teams to accomplish effective results. * Check expiration dates for media ...

PSG Global Solutions

Quality Analyst

Gaithersburg, MD · On-site

... biotechnology and medical companies. As specialists in recognising talent we pride ourselves on not ... Participate in QC project teams to accomplish effective results. * Check expiration dates for media ...

Quality Agents

Automation Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology ... Develop, modify, and troubleshoot automation logic (PLC, SCADA, DCS) in support of process control ...

Quality Agents, LLC

Automation Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology ... control and equipment integration. • Work closely with cross-functional teams on system ...

Quality Agents, LLC

Automation Engineer

Rockville, MD · On-site

Quality Agents, LLC offers validation and quality expertise to the pharmaceutical and biotechnology ... Develop, modify, and troubleshoot automation logic (PLC, SCADA, DCS) in support of process control ...

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All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Washington, DC

Biotech Quality Control information

See Washington, DC salary details

$34.9K

$93.1K

$148.3K

How much do biotech quality control jobs pay per year?

As of Aug 25, 2026, the average yearly pay for biotech quality control in Washington, DC is $93,130.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,300.00 and $114,500.00 per year, depending on experience, location, and employer.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What are the most commonly searched types of Biotech Quality Control jobs in Washington, DC?

The most popular types of Biotech Quality Control jobs in Washington, DC are:

What are popular job titles related to Biotech Quality Control jobs in Washington, DC?

For Biotech Quality Control jobs in Washington, DC, the most frequently searched job titles are:

What job categories do people searching Biotech Quality Control jobs in Washington, DC look for?

The top searched job categories for Biotech Quality Control jobs in Washington, DC are:

Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Washington, DC as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 22% Part Time, 3% Contract, and 1% Nights. Highlights an 80% Physical, 1% Hybrid, and 19% Remote job distribution, with an average salary of $93,130 per year, or $44.8 per hour.

Manager, Quality Control

Precigen, Inc

Germantown, MD • On-site

$105K - $140K/yr

Full-time

Posted 4 days ago

Job description

Job Title: Manager, Quality Control

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.

EOE/MFDV