ZipRecruiter

Log In

1

Gmp Quality Control Jobs in Reston, VA (NOW HIRING)

Precigen, Inc

QC Manager

Germantown, MD · On-site

$95K - $120K/yr

... under GMP guidelines, with demonstrated expertise in multiple disciplines and assays. * 2+ years of supervisory experience. * Advanced experience with QC testing in pharmaceutical or ...

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 ...

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 ...

Merck Group

QC Analyst 1

Rockville, MD · On-site

$23 - $35/hr

As Quality Control Analyst 1, your activities will support assay development through commercial ... Performs basic GMP material control testing on raw materials, finished products and components.

Merck Group

QC Analyst 1

Rockville, MD · On-site

$35/hr

As Quality Control Analyst 1, your activities will support assay development through commercial ... Performs basic GMP material control testing on raw materials, finished products and components.

Merck Group

QC Analyst 1

Rockville, MD · On-site

$23 - $35/hr

As Quality Control Analyst 1, your activities will support assay development through commercial ... Performs basic GMP material control testing on raw materials, finished products and components.

VB Spine

Sr. Quality Engineer

Leesburg, VA · On-site

$100K - $110K/yr

Perform supplier control activities including on-site and desktop audits, maintaining the Approved ... Mentor and train functional groups on GMP, quality concepts, and best practices * Work within the ...

ATCC

Senior Director, Quality

Manassas, VA · On-site

Oversee QC laboratory operations, including method validation and release testing, ensuring ... Progressive Quality leadership experience in ISO- or GMP-compliant organizations providing ...

ATCC

Senior Director, Quality

Manassas, VA

Oversee QC laboratory operations, including method validation and release testing, ensuring ... Progressive Quality leadership experience in ISO- or GMP-compliant organizations providing ...

next page

Showing results 1-20

All JobsGmp Quality Control JobsGmp Quality Control Jobs in Reston, VA

Gmp Quality Control information

See Reston, VA salary details

$12

$22

$34

How much do gmp quality control jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for gmp quality control in Reston, VA is $22.34, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $25.00 per hour, depending on experience, location, and employer.

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 job categories do people searching Gmp Quality Control jobs in Reston, VA look for? The top searched job categories for Gmp Quality Control jobs in Reston, VA are:
What cities near Reston, VA are hiring for Gmp Quality Control jobs? Cities near Reston, VA with the most Gmp Quality Control job openings:
Gmp Quality Control jobs near you

QC Lab Tech (Stability Coordinator) (Pharmaceutical Manufacturing)

Granules Pharmaceuticals

Chantilly, VA • On-site

$19 - $22/hr

Other

Re-posted 6 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.



Apply