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Gmp Quality Control Jobs in Virginia (NOW HIRING)

Kelly Services

Quality Control Technician

Covington, VA · On-site

$20/hr

Quality Control Technician (QC Lab Technician) Kelly ® Science & Clinical is seeking a Quality ... If you're looking to build your career in a GMP laboratory environment and enjoy hands-on ...

advansix

Quality Control Engineer

Chester, VA · On-site

$69K - $103K/yr

Support Quality Control Laboratory operations, including review and validation of analytical ... Familiarity with quality system standards such as ISO 9001, GMP, or ISO 17025. * Excellent ...

advansix

Quality Control Engineer

Chester, VA

$69K - $103K/yr

Support Quality Control Laboratory operations, including review and validation of analytical ... Familiarity with quality system standards such as ISO 9001, GMP, or ISO 17025. * Excellent ...

VB Spine

Quality Control Inspector

Leesburg, VA · On-site

... quality database * Transact parts in the inventory control system (JD Edwards) * Initiate ... Support and follow all company policies, procedures, and GMP requirements * Meet established ...

AdvanSix

Quality Control Engineer

Chester, VA · On-site

$69K - $103K/yr

Support Quality Control Laboratory operations, including review and validation of analytical ... Familiarity with quality system standards such as ISO 9001, GMP, or ISO 17025. * Excellent ...

Akina Pharmacy

Quality Control Technician

Sterling, VA · On-site

$19 - $24.25/hr

Quality Control Technician Company Overview At Akina Pharmacy, the shared purpose that drives us is ... GMP). Collect and analyze data during compounding, filling, or packaging to identify trends or ...

Akina Pharmacy

Quality Control Technician

Sterling, VA · On-site

$19 - $24.25/hr

Quality Control Technician Company Overview At Akina Pharmacy, the shared purpose that drives us is ... GMP). Collect and analyze data during compounding, filling, or packaging to identify trends or ...

Balchem Corporation

Quality Control Lab Technician

Covington, VA · On-site

$16.75 - $21.25/hr

... by GLP/GMP. Apply error recognition and precision analysis to assure accuracy of test results ... Issue the appropriate labels to material handlers that reflect the QC status of material (approved ...

Balchem

Quality Control Lab Technician

Covington, VA · On-site

$16.75 - $21.25/hr

... by GLP/GMP. Apply error recognition and precision analysis to assure accuracy of test results ... Issue the appropriate labels to material handlers that reflect the QC status of material (approved ...

Balchem Corporation

Quality Control Lab Technician

Covington, VA · On-site

$16.75 - $21.25/hr

... by GLP/GMP. Apply error recognition and precision analysis to assure accuracy of test results ... Issue the appropriate labels to material handlers that reflect the QC status of material (approved ...

Vhr_unither

QA/QC Manager - DPF

Christiansburg, VA

... GMP/QSR regulated environment with a Master's Degree - Applied knowledge of GMP/QSR, FDA ... QC microbiology operations - Experience supporting regulatory inspections (FDA, USDA, and other ...

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Gmp Quality Control information

Is GMP quality control inspection a good career?

GMP quality control inspection is a stable career in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training. The role offers opportunities for advancement and consistent employment in regulated environments.

What is the role of quality control in GMP?

In GMP, quality control (QC) is responsible for testing and verifying raw materials, in-process samples, and finished products to ensure they meet specified quality standards. QC helps prevent contaminated or substandard products from reaching consumers and maintains compliance with regulatory requirements through proper documentation and testing procedures.

What is the difference between Gmp Quality Control vs Gmp Quality Assurance?

AspectGmp Quality ControlGmp Quality Assurance
Primary FocusTesting and inspecting products to ensure compliance with standardsDeveloping and maintaining quality systems and processes
ResponsibilitiesSampling, testing, and documenting product qualityAuditing, process validation, and quality system oversight
CertificationsGMP training, laboratory skillsGMP knowledge, quality management system training
Work EnvironmentLaboratories, manufacturing sitesQuality departments, compliance offices

Gmp Quality Control focuses on testing products to verify they meet quality standards, while Gmp Quality Assurance involves establishing and maintaining systems to prevent defects. Both roles are essential in ensuring product safety and compliance in the pharmaceutical and biotech industries.

Is GMP Quality Control a good career?

GMP Quality Control is a vital role in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards through testing and documentation. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training. The career offers stability, opportunities for advancement, and the chance to work in regulated environments that prioritize quality and safety.
What are popular job titles related to Gmp Quality Control jobs in Virginia? For Gmp Quality Control jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Gmp Quality Control jobs in Virginia look for? The top searched job categories for Gmp Quality Control jobs in Virginia are:
What cities in Virginia are hiring for Gmp Quality Control jobs? Cities in Virginia with the most Gmp Quality Control job openings:
Gmp Quality Control jobs near you
Infographic showing various Gmp Quality Control job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.

QC Lab Tech (Stability Coordinator) (Pharmaceutical Manufacturing)

Granules Pharmaceuticals

Chantilly, VA

$19 - $22/hr

Other

Re-posted 5 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.


We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.



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