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Qc Biotech Jobs in Reston, VA (NOW HIRING)

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.

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 ...

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

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 ...

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, 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

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 ...

ATCC

Repository Technician

Gaithersburg, MD

$40K - $50K/yr

Great opportunity to gain biotech industry experience for someone with inventory or warehouse ... Ability to learn and follow quality control and quality assurance procedures. * Effective verbal ...

New

CAMRIS

Quality Assurance Manager

Silver Spring, MD · On-site

$128K - $173K/yr

... material control, staff qualification and training, document origination and control, and ... at a biotechnology, pharmaceutical, or related facility, or an equivalent combination of ...

CAMRIS

Quality Assurance Manager

Silver Spring, MD · On-site

$128K - $173K/yr

... material control, staff qualification and training, document origination and control, and ... at a biotechnology, pharmaceutical, or related facility, or an equivalent combination of ...

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Showing results 1-20

All JobsQc Biotech JobsQc Biotech Jobs in Reston, VA

Qc Biotech information

See Reston, VA salary details

$31.7K

$84.6K

$134.7K

How much do qc biotech jobs pay per year?

As of Aug 9, 2026, the average yearly pay for qc biotech in Reston, VA is $84,605.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,900.00 and $104,000.00 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.
What are popular job titles related to Qc Biotech jobs in Reston, VA? For Qc Biotech jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Qc Biotech jobs in Reston, VA look for? The top searched job categories for Qc Biotech jobs in Reston, VA are:
Qc Biotech jobs near you
Infographic showing various Qc Biotech job openings in Reston, VA as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 5% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $84,605 per year, or $40.7 per hour.

QC Manager

Precigen, Inc

Germantown, MD • On-site

$95K - $120K/yr

Full-time

Re-posted 25 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.