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Qc Associate Scientist Jobs in Virginia (NOW HIRING)

BGDC Distribution

Inventory Control Associate

Salem, VA · On-site

$22/hr

Under the direction of the Quality Control Manager, the Inventory Control Associate is responsible for maintaining accurate inventory records and supporting overall warehouse operations. This role ...

BeiGene USA

Associate Director, QC Microbiology

Hopewell, VA · On-site

$22.75 - $30/hr

When considering candidates, we look for scientific and business professionals who are highly ... Leads and manages all QC Microbiology laboratory activities to support GMP manufacturing, including ...

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All JobsQc Associate Scientist JobsQc Associate Scientist Jobs in Virginia

Qc Associate Scientist information

See Virginia salary details

$18

$35

$56

How much do qc associate scientist jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for qc associate scientist in Virginia is $35.62, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $40.53 per hour, depending on experience, location, and employer.

What is a QC Associate Scientist?

QC Associate Scientists are professionals who work in quality control laboratories, primarily within the pharmaceutical, biotechnology, or related industries. They are responsible for conducting tests and analyses on raw materials, in-process materials, and finished products to ensure they meet established quality standards and regulatory requirements. Their duties often include preparing samples, operating laboratory equipment, documenting results, and assisting in method development and validation. QC Associate Scientists play a crucial role in maintaining product safety and integrity by identifying deviations and supporting investigations. They usually work under the supervision of senior scientists or QC managers.

What are the key skills and qualifications needed to thrive as a QC Associate Scientist?

To thrive as a QC Associate Scientist, you need a strong background in chemistry, biology, or a related field, typically with a bachelor's or master's degree, and experience in laboratory testing and data analysis. Familiarity with analytical instruments (such as HPLC, GC, and PCR), laboratory information management systems (LIMS), and GMP/GLP regulations is essential. Attention to detail, problem-solving abilities, and effective communication skills help ensure accuracy and collaboration within quality control teams. These competencies are vital for maintaining product quality, regulatory compliance, and the integrity of scientific results.

How does a QC Associate Scientist typically collaborate with other teams within a laboratory setting?

As a QC Associate Scientist, you will often work closely with cross-functional teams such as manufacturing, quality assurance, and research and development. Collaboration involves communicating test results, resolving discrepancies, and ensuring that all products meet regulatory and internal quality standards. Regular meetings and data sharing are common, and you may also participate in investigations or troubleshooting efforts when deviations occur. These interactions are key to maintaining workflow efficiency and upholding product integrity.

What is the difference between Qc Associate Scientist vs Qc Analyst?

AspectQc Associate ScientistQc Analyst
Required CredentialsBachelor's degree in Life Sciences, Chemistry, or related field; often some laboratory experienceBachelor's degree in Science; entry-level to mid-level laboratory experience
Work EnvironmentLaboratories within pharmaceutical, biotech, or manufacturing companiesQuality control labs in similar industries, focusing on testing and analysis
Employer & Industry UsageCommonly used in biotech and pharmaceutical industries for product testing and validationWidely used in manufacturing and quality assurance departments across industries

The Qc Associate Scientist and Qc Analyst roles share similar educational backgrounds and work environments, primarily focusing on laboratory testing within the pharmaceutical and biotech sectors. The Associate Scientist often involves more scientific analysis and method development, while the Qc Analyst emphasizes routine testing and data recording. Both roles are essential for maintaining product quality and compliance.

What are popular job titles related to Qc Associate Scientist jobs in Virginia?

For Qc Associate Scientist jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Qc Associate Scientist jobs in Virginia look for?

The top searched job categories for Qc Associate Scientist jobs in Virginia are:

What cities in Virginia are hiring for Qc Associate Scientist jobs?

Cities in Virginia with the most Qc Associate Scientist job openings:

Qc Associate Scientist jobs near you
Infographic showing various Qc Associate Scientist job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $74,082 per year, or $35.6 per hour.

QA/QC Commissioning Associate III

CPG Beyond, Inc.

Ashburn, VA • On-site

$74K - $112K/yr

Full-time

Re-posted 18 hours ago

Job description

TITLE: QA/QC Commissioning Associate III
LOCATION: Ashburn, VA (100 mile Radius) 75%-80% Travel
POSITION SUMMMARY: The QA/QC Commissioning Associate III assists in quality control and quality assurance of data center critical systems preparing for the commissioning process. The QA/QC Commissioning Associate assists the QA/QC Engineer to ensure that the correct equipment has been purchased and that installation is in accordance with industry standards and equipment specifications. This role will develop skills and industry knowledge to perform increasingly more complex commissioning tasks.
ESSENTIAL DUTIES AND RESPONSIBILITIES: To perform this job successfully, an individual must be able to perform the following satisfactorily; other duties may be assigned. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Develop QA/QC documents of the complete project including certificates, calibration, test results, inspection requests, non-compliance reports and site instruction/observations, permanent materials delivered, and other important QA/QC documents
  • Follow all standards to perform inspection and tests on all procedures and oversee all testing methods and maintain high standards of quality for all processes
  • Review the quality of all materials at the site and ensure compliance with all project specifications and quality and collaborate with the department for all material procurement and maintain a quality of materials
  • Support the effective implementation of all test and inspection schedules and ensure adherence to all procedures and coordinate with various teams to perform quality audits on processes
  • Assist employees to ensure knowledge of all quality standards and ensure compliance to all quality manuals and procedures and collaborate with contractors and suppliers to maintain the quality of all systems
  • Manage to lift all types of equipment and handle the efficient storage of all hazardous materials and perform quality audits as per the required schedule
  • Understand all products and non-conformance processes and evaluate all documents to ensure the maintenance of optimal quality and prepare monthly reports to evaluate performance
  • Monitor an efficient system and record for all project activities and analyze all processes to ensure all work according to quality requirements
  • Understand all work methods and maintain knowledge on all quality assurance standards and monitor continuous application for all quality assurance processes and recommend corrective actions for all processes
  • Support and follow a method statement for the activity including risk assessment and job safety environmental analysis and Inspection Test Plan and Checklist based on specifications of the project
  • Liaise the Technical Engineer for submission of material submittals to Consultant
  • Develop and maintain inspection reports
  • Ensure compliance to federal and state laws, as well as company standards and specifications
  • Maintain calibration of quality testing equipment
  • Perform inspections across all stages of production
  • Advising on procedures to improve production efficiency
  • Prepare and maintain test data for review
  • Evaluate data and draft reports, noting any relevant deviations from existing standards
  • Identify areas for quality control improvement and implement new methods accordingly
  • Communicate quality or compliance concerns with urgency

QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education/Experience (Desired):
  • Technical Military MOS, trade school and/or degree
  • Experience and/or education and internship in complex facilities or mission critical projects is preferred
  • Any civilian or military technical certifications is a plus
  • Experience with writing and enforcing standard operating procedures (SOPs)
  • Solid understanding of test equipment amp; software
  • Minimum of 5-9 years of inspection and/or production experience
  • Strong working knowledge of various mathematical concepts including fractions, ratios, and proportions
  • Demonstrated ability to work independently with minimal supervision
  • Excellent organizational skills
  • Demonstrated ability to analyze and interpret information
  • Must be able to travel 75%-80%
  • Must be a US citizen
Computer Skills:
  • Advanced Excel skills preferred
  • Experience using Microsoft Office Suite, Word and Microsoft Project
  • Basic knowledge of systems design for various projects
Certificates and Licenses:
  • No certificates or licenses required
Supervisory Responsibilities:
  • No supervisory responsibilities for this position.
Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Occasionally lift and or move objects 10 to 50; Frequently required to stand, walk, stoop, kneel, crouch or crawl. The employee is occasionally required to sit and climb or balance. Specific vision abilities for this job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust and focus. Noise Level can be moderate to high.
The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor.
Pre Employment Requirements:

Employment is contingent upon successful completion of a pre-employment background check, drug screening, and motor vehicle record (MVR) review, in accordance with applicable federal, state, and local laws. Positions requiring driving must have an MVR that meets company and insurance carrier standards.

CPG is an equal opportunity employer. We will consider all employment applicants without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
CPG Participates in E-Verify
#:LI-TG1

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