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Quality Control Stability Analyst Jobs in Virginia

LSI Staffing

Quality Control

Mechanicsville, VA

$21/hr

Quality control Night Shift - 6:45pm to 7am / Pay rate: $22/hr Bilingual applicants are encouraged ... Perform Root Cause Analysis on process and product failures. ? Set an example for best practices ...

Granules

Quality Control Manager

Chantilly, VA · On-site

Supervise the testing of bulk release, finished product and stability testing * Manage and supervise QC laboratory personnel with varying levels of experience, assigning the work schedule and ensure ...

LSI Staffing

Quality Control

Midlothian, VA · On-site

$21/hr

Quality control Night Shift - 6:45pm to 7am / Pay rate: $22/hr Bilingual applicants are encouraged ... Perform Root Cause Analysis on process and product failures. ? Set an example for best practices ...

New

LSI Staffing

Quality Control

Richmond, VA · On-site

$21/hr

Quality control Night Shift - 6:45pm to 7am / Pay rate: $22/hr Bilingual applicants are encouraged ... Perform Root Cause Analysis on process and product failures. ? Set an example for best practices ...

RecruitTalent LLC.

Quality Control

Norfolk, VA · On-site

$50 - $60/hr

... requires strong analytical skills, technical proficiency, and a service-first mindset ... Perform quality control audits on Fleet mishap and hazard records to ensure data integrity and ...

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Quality Control Stability Analyst information

What are Quality Control Stability Analysts?

Quality Control Stability Analysts are professionals responsible for testing and evaluating the stability of pharmaceutical products over time. They design, conduct, and interpret experiments to ensure products maintain their safety, potency, and quality throughout their shelf life. Their work is crucial for regulatory compliance, as they document and report stability data according to industry standards and guidelines. These analysts often work in laboratory environments and collaborate closely with quality assurance and manufacturing teams.

What are the key skills and qualifications needed to thrive as a Quality Control Stability Analyst, and why are they important?

To thrive as a Quality Control Stability Analyst, you need a solid background in chemistry or related sciences, familiarity with Good Laboratory Practices (GLP), and often a relevant bachelor's degree. Experience with laboratory instrumentation such as HPLC, GC, and LIMS, along with knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure accurate data analysis, compliance with regulations, and reliable stability testing to maintain product quality and safety.

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

AspectQuality Control Stability AnalystQuality Control Analyst
CertificationsGMP, GLP, relevant laboratory certificationsGMP, GLP, relevant laboratory certifications
Work EnvironmentPharmaceutical, biotech labs focusing on stability testingManufacturing labs, quality testing environments
Job FocusMonitoring product stability over time, data analysis for stability programsPerforming routine quality tests, raw material and finished product testing

The main difference is that a Quality Control Stability Analyst specializes in stability testing and data analysis related to product shelf life, while a Quality Control Analyst performs general quality testing. Both roles require similar certifications and work in related environments, but their focus areas differ within the quality assurance process.

What are some typical challenges faced by Quality Control Stability Analysts, and how can they be addressed?

Quality Control Stability Analysts often face challenges such as managing multiple projects with tight timelines, accurately interpreting stability data, and ensuring compliance with stringent regulatory requirements. Balancing the need for meticulous documentation with the fast-paced nature of product development can also be demanding. To address these challenges, analysts benefit from strong organizational skills, effective communication with cross-functional teams (like R&D and production), and ongoing training on evolving industry standards and regulatory guidelines.
What are popular job titles related to Quality Control Stability Analyst jobs in Virginia? For Quality Control Stability Analyst jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability Analyst jobs in Virginia look for? The top searched job categories for Quality Control Stability Analyst jobs in Virginia are:
What cities in Virginia are hiring for Quality Control Stability Analyst jobs? Cities in Virginia with the most Quality Control Stability Analyst job openings:
Quality Control Stability Analyst jobs near you
Infographic showing various Quality Control Stability Analyst job openings in Virginia as of June 2026, with employment types broken down into 73% Full Time, 19% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

QC Lab Tech (Stability Coordinator) (Pharmaceutical Manufacturing)

Granules Pharmaceuticals

Chantilly, VA • On-site

$20.50 - $25.75/hr

Other

Posted 11 days ago

Job description

Description

Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!

With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.

Job Summary:

Perform a variety of activities to administer the stability program and manage data generated in support of the company's quality program. 

Essential Responsibilities:

  • Comply with the requirements of stability standard operating procedure.
  • Data entry and usage of stability software.
  • Review stability program annually and recommend revision when necessary.
  • Provide stability summary to QC Director upon completion of study.
  • Assures that stability samples are disposed of according to GMP guidelines.
  • Will assist in preparing and maintaining batch records, certificate of analysis, maintain/control and file records of raw material specification and finished product specification.
  • Responsible for ensuring stability chambers and monitoring system are performing within set requirements. 
  • Employee uses professional skills and concepts to solve a variety of often complex situations. Able to make clear and concise decisions of vast importance in limited period of time. Must be able to perform multiple tasks in the proper sequence to effectively reach desired goals.

Requirements:

  • Minimum Associate's Degree, Bachelor's degree preferred in pharmacy, chemistry or related scientific field
  • 0-2 years' experience in Quality control laboratory.
  •  Knowledge of and ability to work with equipment, supplies, components and technical areas that are utilized in the    pharmaceutical industry.
  • Knowledge of FDA guidelines on Stability requirements is a plus;
  • Must be able to analyze data and work with a high degree of accuracy; 
  • Organized and able to perform duties in a timely manner; 
  • Must be flexible and able to handle multiple activities;
  • Must have excellent computer skills and verbal and written commutation skills.
  • Must be able to work in a team environment; team player.

Additional Preferred: 

  •  Experience in GMP quality control and/or pharmaceutical manufacturing facility; 
  • Pharmaceutical stability operations experience

Physical Conditions


Long periods of sitting, standing, walking, bending, stooping, reaching, and lifting. Will work around powders and other chemicals. Protective eyewear is necessary to wear in the laboratory or manufacturing.

Requirements

Preferred Knowledge & Skills:

  • Strong knowledge of the major analytical techniques: HPLC/UPLC, GC, dissolution, etc. FT-IR, FDA/ICH regulations.
  • Solid knowledge of FDA/ICH regulations.

Required Experience & Education:

  • BS or MS in Chemistry, Pharmacy, Biochemistry, Biology or Biotechnology or related field.
  • Minimum 2 - 5 years of experience in using analytical instrument techniques including HPLC/GC/FT-IR, UV-Vis, Dissolution Apparatus, Ovens/Auto Titrators/KF Titrator/Particle size analyzers/ Ion-Chromatography.

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