ZipRecruiter

Log In

1

Qc Biotech Jobs in Washington (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 ...

New

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

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 ...

next page

Showing results 1-20

All JobsQc Biotech JobsQc Biotech Jobs in Washington

Qc Biotech information

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 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 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 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 popular job titles related to Qc Biotech jobs in Washington?

For Qc Biotech jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Qc Biotech jobs in Washington look for?

The top searched job categories for Qc Biotech jobs in Washington are:

Qc Biotech jobs near you
Infographic showing various Qc Biotech job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 5% Part Time, 2% Temporary, 7% Contract, and 1% Nights. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution.

Manager, Quality Control

Precigen, Inc

Germantown, MD • On-site

$105K - $140K/yr

Full-time

Posted yesterday

New

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