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Quality Control Stability Jobs in Virginia (NOW HIRING)

The QA/QC Manager makes sure that system holds: inspection and testing are done and recorded ... Internal/External Success Rate, Order Shipment Success Rate, corrective action reports, stability ...

The QA/QC Manager makes sure that system holds: inspection and testing are done and recorded ... Internal/External Success Rate, Order Shipment Success Rate, corrective action reports, stability ...

Observes and documents QC/QA activities to verify compliance with the Quality Management Plan ... stability throughout the employee's career. At WSP, we want to give our employees the challenges ...

Observes and documents QC/QA activities to verify compliance with the Quality Management Plan ... stability throughout the employee's career. At WSP, we want to give our employees the challenges ...

Analyze process capability, stability, and failure modes using data-driven methods to improve ... Identify gaps in process capability, control, and reliability, and coordinate actions to address ...

New

The Quality Systems Coordinator supports product release and testing activities by managing ... control activities. Support product release, commercial stability, end-of-shelf-life, and finished ...

Software Quality Engineer

Staunton, VA · On-site

$70K - $110K/yr

Validate REST APIs and shared schema layers (such as Zod) with a focus on contract stability ... control. * Conduct post-release and post-implementation verification testing in production ...

Software Quality Engineer

Staunton, VA · On-site

$70K - $110K/yr

Validate REST APIs and shared schema layers (such as Zod) with a focus on contract stability ... control. * Conduct post-release and post-implementation verification testing in production ...

Develop and maintain the Program Management Plan, Risk Register, and Quality Control Program ... Oversee transition/phase-in and workforce stability. Minimum Requirements * Bachelor's degree in ...

Develop and maintain the Program Management Plan, Risk Register, and Quality Control Program ... Oversee transition/phase-in and workforce stability. Minimum Requirements * Bachelor's degree in ...

Analytical Scientist I

Lynchburg, VA · On-site

$58K - $94K/yr

Coordinate with QA/QC groups and contract manufacturers and laboratories for method transfer and supporting tests. Ensures the proper documentation of such methods. Prepare stability test reports ...

Coordinate with QA/QC groups and contract manufacturers and laboratories for method transfer and supporting tests. Ensures the proper documentation of such methods. Prepare stability test reports ...

Coordinate with QA/QC groups and contract manufacturers and laboratories for method transfer and supporting tests. Ensures the proper documentation of such methods. Prepare stability test reports ...

... Change Control, CAPA's (including verification of CAPA's) and other quality documents as needed ... specifications, stability reports, technical reports (i.e., Qualification, Validation ...

Responsible for Control and management of stability, retain and reject materials. * Assist in ... Reports to QA Manager Requirements: Knowledge & Skills * cGMP compliance within the pharmaceutical ...

Showing results 41-60

Quality Control Stability information

What is a quality control stability role?

A Quality Control Stability role involves monitoring and evaluating the stability of pharmaceutical products, ensuring they maintain their quality, safety, and efficacy throughout their shelf life. Professionals in this position design and execute stability studies, analyze the results, and document findings according to regulatory requirements. They play a crucial part in ensuring compliance with industry standards and supporting product development and release. This role typically requires expertise in analytical testing, regulatory guidelines, and laboratory practices.

What are some common challenges faced in a quality control stability role, and how can they be addressed?

Professionals in Quality Control Stability often encounter challenges such as managing tight timelines for stability testing, interpreting ambiguous results, and ensuring compliance with evolving regulatory requirements. Effective communication with cross-functional teams—such as R&D, production, and regulatory affairs—is essential to address discrepancies and maintain data integrity. Staying organized, maintaining thorough documentation, and keeping up to date with industry guidelines help mitigate these challenges and ensure smooth workflow.

What are the key skills and qualifications needed to thrive as a quality control stability specialist, and why are they important?

To thrive as a Quality Control Stability specialist, you need a solid background in chemistry or related sciences, experience with stability testing, and typically a bachelor’s degree in a scientific field. Familiarity with laboratory instruments (such as HPLC, GC), stability management systems, and knowledge of regulatory guidelines like ICH are essential. Attention to detail, problem-solving, and strong organizational skills help ensure accurate data analysis and effective reporting. These abilities are crucial for maintaining compliance, product safety, and reliability in pharmaceutical or biotech environments.

What is the difference between Quality Control Stability vs Quality Control Inspector?

AspectQuality Control StabilityQuality Control Inspector
CertificationsOften requires certifications like Six Sigma, ISO auditor, or quality management certificationsTypically requires quality inspection certifications or training
Work EnvironmentFocuses on maintaining process stability in manufacturing or production settingsPerforms inspections on products or materials on the production line
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and industries emphasizing process consistencyCommon in manufacturing, food production, and assembly lines

Quality Control Stability involves ensuring that manufacturing processes remain consistent over time, emphasizing process control and reduction of variability. In contrast, a Quality Control Inspector primarily conducts inspections to verify product quality at various stages. Both roles are essential in quality management but focus on different aspects of quality assurance.

Is quality control stability a good career choice?

Quality Control Stability is a role focused on maintaining product consistency and compliance through testing and monitoring processes. It often requires attention to detail, knowledge of industry standards, and proficiency with testing tools or software. This career can offer steady employment opportunities in manufacturing, pharmaceuticals, or food industries, with potential for advancement and certification.

Is quality control stability a good career path?

Quality control stability involves ensuring products meet quality standards over time, often requiring attention to detail and knowledge of testing procedures. It can offer steady employment and opportunities for advancement in manufacturing, pharmaceuticals, or food industries, especially for those with relevant certifications or experience. The career can be stable, but growth depends on industry demand and individual skill development.

What are popular job titles related to Quality Control Stability jobs in Virginia?

For Quality Control Stability jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Quality Control Stability jobs in Virginia look for?

The top searched job categories for Quality Control Stability jobs in Virginia are:

What cities in Virginia are hiring for Quality Control Stability jobs?

Cities in Virginia with the most Quality Control Stability job openings:

QAQC Manager

Ridgeway, VA • On-site

Brown and Root
Engineering Professional Services • 5 - 10K employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago


Brown & Root rating

6.9

Company rating: 6.9 out of 10

Based on 46 frontline employees who took The Breakroom Quiz


Job description

POSITION SUMMARY

The QA/QC Manager owns the ISO 9001:2015 Quality Management System (QMS) at our Martinsville, VA manufacturing support operation. The site works as a dedicated contract supplier providing Composite Services Processing (CSP) to industrial manufacturing customers.

Customers supply the product instructions and the criteria that must be met. Work is broken into stages so trained employees verify conformity before product moves forward. The QA/QC Manager makes sure that system holds: inspection and testing are done and recorded, records are complete and accurate, nonconforming product is contained, and corrective action closes the loop. The role carries the authority to authorize the quality system and its revisions.

KEY RESPONSIBILITIES

Quality management system ownership

  • Ensure implementation and maintenance of the QMS, along with supporting quality reports.
  • Authorize the quality system and all quality system revisions.
  • Maintain the integrity of the QMS when changes are planned and implemented.
  • Report QMS performance and improvement opportunities to top management.
  • Initiate new standard operating procedures (SOPs) and approve changes to existing SOPs (SOP-105, SOP-107).
  • Provide the ISO registrar with uncontrolled copies of SOPs. Support registrar and customer audits.
  • Promote customer focus and engage personnel across the operation in QMS principles.

Inspection, testing, and product conformity

  • Ensure product inspection and testing is conducted and recorded to meet or exceed customer requirements (SOP-547, SOP-547A).
  • Ensure the current version of customer specifications is in use (SOP-122).
  • Verify stage-by-stage conformity so product does not advance until requirements are met.
  • Maintain product identification and traceability controls (SOP-547-A, SOP-531A).
  • Support accurate, on-time shipments with complete job order documentation.

Calibration and measurement systems

  • Set and approve equipment calibration intervals and procedures with the QA/Calibration Technician (SOP-532A).
  • Ensure inspection, measuring, and test equipment carries a unique control number, is labeled, and is calibrated on schedule using equipment traceable to NIST or equivalent.
  • Ensure expired or suspect equipment is identified, removed from use, and reported to department management.
  • Oversee measurement system studies (SOP-536B) and capability studies performed at customer direction.

Nonconformance, corrective action, and improvement

  • Initiate nonconformance reports.
  • Control further processing, delivery, or installation of nonconforming product until unsatisfactory conditions are corrected.
  • Administer the Corrective Action System (SOP-551) and Preventive Action System (SOP-535): containment, root cause analysis, disposition, and customer notification.
  • Verify that solutions to quality issues are implemented and effective.
  • Maintain corrective action reports and related records.

Audits, data, and management review

  • Plan and run the internal audit program (SOP-114) on the monthly cycle, with impartial auditors, defined scope and criteria, and results reported to management without undue delay.
  • Serve with the General Manager as the quorum for monthly management review of the QMS.
  • Track and report QMS effectiveness measures monthly, and deliver the quarterly Quality Performance Analysis Review: Internal/External Success Rate, Order Shipment Success Rate, corrective action reports, stability testing, and CPK values.
  • Monitor customer satisfaction inputs including the semi-annual survey, customer nonconformance reports, customer portals, and customer scorecards.

Documented information and training

  • Control quality system documentation and record retention (SOP-107, SOP-145).
  • Identify and provide training for department personnel on department operations, SOPs, safety rules, and the quality system (SOP-203).
  • Issue monthly training schedules to department management and maintain department training records.
  • Coordinate quality system activity with QA technicians and department management.

Customer, supplier, and resource interface

  • Act as the quality point of contact for customer specifications, complaints, and audits.
  • Conditionally approve new vendors and subcontractors (SOP-108) and approve purchase orders (SOP-112).
  • Coordinate quality resource, equipment, and staffing needs with department management.

QUALIFICATIONS

Education and experience

  • Bachelor's degree in engineering, quality management, industrial technology, or a related technical field preferred. Equivalent experience will be considered.
  • Five or more years of quality experience in manufacturing, contract manufacturing, or precision machining and composites operations.
  • Two or more years supervising quality personnel.
  • Hands-on experience maintaining an ISO 9001 certified QMS, including registrar and customer audits.
  • Experience working to customer-supplied specifications in a dedicated supplier or contract services model.

Certifications

  • ISO 9001:2015 Lead Auditor certification, or the ability to obtain within the first year.
  • ASQ CMQ/OE (Certified Manager of Quality), CQE, or CQA preferred.
  • Six Sigma Green Belt or Black Belt preferred.

Skills

  • Working knowledge of ISO 9001:2015 clause requirements and how to evidence conformity.
  • SPC, CPK and process capability analysis, measurement system analysis, and Gage R&R.
  • Root cause analysis methods such as 5 Why and cause-and-effect analysis, plus FMEA.
  • Ability to read, interpret, and work from blueprints, customer specifications, and sketches, including GD&T callouts, tolerances, and revision levels.
  • Hands-on skill with micrometers, calipers, gage pins, height gages, indicators, and comparable inspection equipment.
  • Technical writing for SOPs, work instructions, and inspection control plans.
  • Proficiency in MS Office and quality data systems, including customer portals and scorecards.
  • Clear communication with operators, management, customers, and auditors.
  • Disciplined recordkeeping and strong attention to detail.

PHYSICAL REQUIREMENTS AND WORK ENVIRONMENT

  • Regular presence on the manufacturing and warehouse floor, wearing required PPE and following SOP-813 General Safety Policy.
  • Standing, walking, bending, and lifting up to 25 pounds, with close vision work for inspection tasks.
  • Occasional travel to customer or supplier locations.

Brown & Root Industrial Services is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, disability, sex, sexual orientation, gender identity or expression, age, national origin, veteran status, genetic information, union status and/or beliefs, or any other characteristic protected by federal, state, or local law. BENEFITS: Brown and Root offers a selection of competitive lifestyle benefits which include a 401K plan with company match, medical, dental, vision, life insurance, AD&D, flexible spending account, disability, paid time off, and flexible work schedule. We support career advancement through professional training and development.


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About Brown & Root

Sourced by ZipRecruiter

Brown & Root is a prominent player in the industrial service industry, with their headquarters nestled in Baton Rouge, Louisiana, US. With a substantial history dating back to 1919, the company has built a reputation for delivering comprehensive solutions to their customers, primarily in engineering, construction, maintenance, operations, and other related industrial services. Brown & Root’s core mission is echoed in their commitment to safety, customer satisfaction, integrity, and delivering high-quality services. They also take pride in their culture of continuous improvement which has yielded significant achievements such as earning a spot in the Engineering News-Record's top 400 contractors list.

Industry

Engineering professional services

Company size

5,001 - 10,000 Employees

Headquarters location

Baton Rouge, LA, US

Year founded

1919