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Quality Systems Associate Jobs in Virginia (NOW HIRING)

... associates on daily issues. · Enter and track quality results in computerized systems. · Comply with SQF, Food Safety Plan (HACCP), and Food Quality Plan (FQP) standards. · Ensure compliance with ...

Senior Systems Engineer

Reston, VA · On-site

$108K - $148K/yr

The successful candidate will have a primary interest in high-quality systems engineering. Job Responsibilities • Support integration and testing on-site at the integration facility • Perform ...

Senior Systems Engineer

Reston, VA · On-site

$108K - $148K/yr

The successful candidate will have a primary interest in high-quality systems engineering. Job Responsibilities • Support integration and testing on-site at the integration facility • Perform ...

Senior Systems Engineer

Reston, VA · On-site

$108K - $148K/yr

The successful candidate will have a primary interest in high-quality systems engineering. Job Responsibilities • Support integration and testing on-site at the integration facility • Perform ...

Senior Systems Engineer

Reston, VA · On-site

$108K - $148K/yr

The successful candidate will have a primary interest in high-quality systems engineering. Job Responsibilities • Support integration and testing on-site at the integration facility • Perform ...

Identify opportunities to improve quality systems and streamline processes across CAPA, document ... OR Associate degree in a science-related field with 1+ years of relevant experience. * Demonstrated ...

Identify opportunities to improve quality systems and streamline processes across CAPA, document ... OR Associate degree in a science-related field with 1+ years of relevant experience. * Demonstrated ...

Identify opportunities to improve quality systems and streamline processes across CAPA, document ... OR Associate degree in a science-related field with 1+ years of relevant experience. * Demonstrated ...

Support Integrated Management System requirements and comply with applicable quality, safety ... Associate degree or technical certification in Quality, Manufacturing, Engineering Technology ...

Showing results 41-60

Quality Systems Associate information

What is the difference between Quality Systems Associate vs Quality Control Technician?

AspectQuality Systems AssociateQuality Control Technician
CertificationsISO auditor, GMP, or quality management certificationsGMP, HACCP, or industry-specific testing certifications
Work EnvironmentDocument control, quality management systems, auditsProduct testing, inspection, sampling
Employer & Industry UsageManufacturing, pharmaceuticals, biotechFood, pharmaceuticals, manufacturing

The Quality Systems Associate focuses on maintaining and improving quality management systems, documentation, and compliance. In contrast, the Quality Control Technician primarily conducts product testing and inspections to ensure quality standards are met. Both roles are essential in quality assurance but differ in their core responsibilities and daily tasks.

Is a Quality Systems Associate an entry level job?

A Quality Systems Associate position is often considered entry level, suitable for candidates with a bachelor's degree in a related field and some familiarity with quality management systems like ISO or GMP. The role typically involves supporting quality processes, documentation, and audits, and may require basic knowledge of tools such as SAP or TrackWise. Experience requirements vary by employer, but many entry-level candidates can qualify with relevant internships or certifications.

What is a quality systems associate?

A quality systems associate is responsible for maintaining and improving a company's quality management system, ensuring compliance with industry standards such as ISO 9001. They often perform audits, document control, and data analysis, and may use tools like quality management software to support continuous improvement efforts.

What are the most commonly searched types of Quality Systems jobs in Virginia?

The most popular types of Quality Systems jobs in Virginia are:

Infographic showing various Quality Systems Associate job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution.

QA Ops Shop Floor Associate (386)

Petersburg, VA • On-site

Civica Rx
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees

$65K - $75K/yr

Full-time

Re-posted 14 hours ago


Job description

Position Summary:

The Quality Assurance Operations Shop Floor Associate is part of the Quality Assurance Operations team at Civica’s Petersburg, Virginia manufacturing facility. The Petersburg site serves as Civica’s new fill-finish facility dedicated to the manufacture and supply of essential generic sterile injectable medications. This role will function to ensure ongoing compliance with cGMP requirements on the manufacturing floor.

Key Responsibilities:

  • Provide Quality Assurance oversight on the manufacturing floor during all operations regarding procedures, reports, batch records, aseptic technique, gowning, nonconformances, product sampling, and/or other records as necessary to support the manufacturing processes.
  • On-the-floor review of batch records during execution to ensure compliance with approved procedures, as well as communicate and resolve discrepancies with manufacturing operators and/or supervisors.
  • Familiarity with electronic management systems such as Veeva, Deacom, and Blue Mountain RAM.
  • Facilitate Quality oversight on the shop floor through walkthroughs, Gemba, and process observations to ensure full adherence to cGMP practices.
  • Identify and implement improvements to procedures and processes as part of broader continuous improvement initiatives.

Essential Duties and Responsibilities:

  • Working across functions to ensure operational compliance in all aspects of product manufacturing.
  • Enforcing adherence to all Civica standard operating procedures (SOPs) while on the manufacturing floor.
  • Promote a quality mindset and quality excellence approach to all activities.
  • Promote a safety mindset and focus on safety for all operations activities.
  • Ensure that on-the-floor review of manufacturing records, batch quantities, and accountability calculations are performed and completed accurately.
  • Provide immediate support in the identification and documentation of nonconformances, deviations, or discrepancies on the manufacturing floor.
  • Provide support as required to all manufacturing and processing areas within the facility, depending on job assignment and schedule.

Basic Qualifications and Capabilities:

  • Bachelor's degree or above in a scientific discipline.
  • Minimum of 2+ years of experience within a pharmaceutical, biotech, cell therapy, or medical device cGMP-regulated manufacturing environment.
  • Experience in sterile pharmaceutical isolator technology, combination products, or medical devices.
  • Demonstrated experience delivering training on cGMP regulations, SOPs, and quality systems.
  • Excellent written and verbal skills and ability to present technical data effectively based on target audience.
  • Ability to work in a fast-paced team environment and lead peers through changing priorities.
  • Detail-oriented and task-focused with the ability to meet deadlines and support work prioritization.

Physical Demands and Work Environment:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions.

While performing the essential duties of this position, the employee is regularly required to speak or hear. The employee frequently is required to use hands or fingers, handle or feel objects, tools, or controls. The employee is occasionally required to stand; walk; sit; and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities this position requires include close vision, distance vision, and the ability to adjust focus. The noise level in the work environment is usually low to moderate. 

The company is an Equal Opportunity Employer, a drug-free workplace, and complies with ADA regulations as applicable.


Civica Rx logo

About Civica Rx

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

51 - 200 Employees

Headquarters location

Lehi, UT, US

Year founded

2018