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Senior Qc Analyst Jobs in Silver Spring, MD (NOW HIRING)

Precigen, Inc

Manager, Quality Control

Germantown, MD · On-site

$105K - $140K/yr

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 ...

Precigen

Manager, Quality Control

Germantown, MD · On-site

$105 - $140/hr

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 ...

CACI

Program Control Analyst, Senior

Springfield, VA · On-site

$121K - $121K/yr

Job Title: Program Control Analyst, Senior Job Category: Finance and Accounting Time Type ... Our employees value the flexibility at CACI that allows them to balance quality work and their ...

CACI

Senior Quality Manager

Reston, VA · On-site

... quality control procedures, training materials, and lessons learned Implements continuous ... analysis, and implementing corrective and preventive actions Demonstrated experience leading ...

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All JobsQc Analyst JobsSenior Qc Analyst JobsSenior Qc Analyst Jobs in Silver Spring, MD

Senior Qc Analyst information

See Silver Spring, MD salary details

$55.3K

$113.6K

$147.3K

How much do senior qc analyst jobs pay per year?

As of Sep 7, 2026, the average yearly pay for senior qc analyst in Silver Spring, MD is $113,557.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,600.00 and $141,600.00 per year, depending on experience, location, and employer.

What is a senior QC analyst?

Senior QC (Quality Control) Analysts are experienced professionals responsible for overseeing and conducting quality control tests in laboratories, typically within the pharmaceutical, biotechnology, or manufacturing industries. They ensure that products meet required standards and specifications by performing analytical tests, reviewing data, and troubleshooting issues. Senior QC Analysts also mentor junior staff, help develop testing methods, and ensure compliance with regulatory guidelines such as GMP (Good Manufacturing Practices). Their role is crucial in maintaining product quality and safety before products reach consumers.

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

To thrive as a Senior QC Analyst, you need a strong background in analytical chemistry or life sciences, experience with quality control procedures, and typically a bachelor's degree or higher in a related field. Familiarity with laboratory instrumentation (such as HPLC, GC, or FTIR), LIMS software, and regulatory requirements like GMP and FDA guidelines is essential. Attention to detail, problem-solving, and effective communication skills help you lead investigations and mentor junior staff. These skills are crucial for ensuring product quality, regulatory compliance, and efficient laboratory operations.

What are some common challenges faced by senior QC analysts, and how can they be addressed?

Senior QC Analysts often encounter challenges such as managing tight project deadlines, ensuring compliance with evolving regulatory standards, and troubleshooting unexpected laboratory issues. Successfully navigating these challenges requires strong organizational skills, up-to-date knowledge of industry regulations, and effective communication with cross-functional teams. Building robust documentation processes and fostering a culture of continuous improvement can also help Senior QC Analysts maintain high-quality results while adapting to changing project needs.

What is the difference between Senior Qc Analyst vs Quality Control Technician?

AspectSenior Qc AnalystQuality Control Technician
Required CredentialsBachelor's degree, often with certifications like CQEAssociate's or Bachelor's degree, sometimes with certifications
Work EnvironmentLaboratories, manufacturing plants, quality departmentsManufacturing sites, labs, production lines
Employer & Industry UsagePharmaceuticals, biotech, manufacturingManufacturing, food production, pharmaceuticals
Job ResponsibilitiesData analysis, process improvement, oversightTesting, sampling, data recording

The Senior Qc Analyst typically has more advanced responsibilities, including data analysis and process improvements, while the Quality Control Technician focuses on testing and sampling tasks. Both roles are essential in quality assurance within manufacturing and biotech industries.

What are popular job titles related to Senior Qc Analyst jobs in Silver Spring, MD?

For Senior Qc Analyst jobs in Silver Spring, MD, the most frequently searched job titles are:

What cities near Silver Spring, MD are hiring for Senior Qc Analyst jobs?

Cities near Silver Spring, MD with the most Senior Qc Analyst job openings:

Senior Qc Analyst jobs near you
Infographic showing various Senior Qc Analyst job openings in Silver Spring, MD as of August 2026, with employment types broken down into 1% Internship, 81% Full Time, 11% Part Time, and 7% Contract. Highlights an 80% Physical, 10% Hybrid, and 10% Remote job distribution, with an average salary of $113,557 per year, or $54.6 per hour.

Manager, Quality Control

Precigen, Inc

Germantown, MD • On-site

$105K - $140K/yr

Full-time

Posted 17 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