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Quality Control Pharma Jobs in Virginia (NOW HIRING)

Granules

Quality Control Manager

Chantilly, VA · On-site

$100K - $120K/yr

... pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through ... Manage and supervise QC laboratory personnel with varying levels of experience, assigning the work ...

Granules

Biochemist I/II (QC Analyst)

Chantilly, VA · On-site

$55K - $80K/yr

... pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through ... The role of Biochemist I/II (QC Analyst) is responsible for supporting the operations and ...

Catalent Pharma Solutions

Maintenance Mechanic

Manassas, VA

$25 - $32/hr

... Quality Plan (FQP.) * Other duties as assigned. The Candidate * Associate degree with 2+ years of ... Technicians should be able to run conduit and wire electrical control panels according to NEC ...

Granules

Formulation Scientist (Solid Orals)

Chantilly, VA · On-site

$100K - $110K/yr

... pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through ... Coordinate with Regulatory Affairs, Operations, QC/QA and Supply Departments to ensure that ...

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Quality Control Pharma information

What are the key skills and qualifications needed to thrive as a Quality Control professional in the pharmaceutical industry, and why are they important?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What is Quality Control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

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

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

What are some of the common challenges faced by Quality Control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.
What are popular job titles related to Quality Control Pharma jobs in Virginia? For Quality Control Pharma jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Quality Control Pharma jobs in Virginia look for? The top searched job categories for Quality Control Pharma jobs in Virginia are:
What cities in Virginia are hiring for Quality Control Pharma jobs? Cities in Virginia with the most Quality Control Pharma job openings:
Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma job openings in Virginia as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 2% Temporary, and 2% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Quality Control Manager

Granules Pharmaceuticals

Chantilly, VA • On-site

$100K - $120K/yr

Full-time

Posted 6 days ago

Job 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
Supervise the work of laboratory personnel engaged in performing routine finished product testing & stability testing, including planning laboratory work, evaluating work performed and handling procedural and technical laboratory problems. Execute according to high standards of quality at the lab through managing and continuously improving the effectiveness of laboratory quality processes and systems
Job Duties & Responsibilities
  • 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 assigned tasks are performed.
  • Review of test results for accuracy and proper documentation.
  • Review of specifications and STMs for in process and finished products.
  • Write OOS investigations, including finding root cause and corrective/preventive actions.
  • Supervise lab processes, including timely management of investigations, CAPA implementation to ensure sustainable compliance
  • Review of SOPs, lab related investigations, stability failure notifications, COAs, and compilation of stability related data. Responsible for timely release of in-process, finished product release COA's
  • Monitor and report the trends in bulk, finished products, and stability samples to QC/QA Management
  • Review of IQ, OQ, and PQ for new instruments, protocols/reports
  • Responsible for coordinating with other departments like warehouse, QA, Maintenance, purchase department, R&D in day to day activity for better operational requirements and to follow the cGMP requirements.
  • Responsible for the coordination of sample management, not limited to in-process, finished product and stability samples.
  • Monitor Quality Control, Safety and cGMP practices to assure compliance with internal and external regulations.
  • Perform other related duties as assigned to meet departmental and Company objectives.

Management Responsibility
  • Manage group of scientists.

Reports to
  • Associate Director / Director

Requirements
Knowledge & Skills
  • Ability to maintain integrity and honesty at all times
  • Ability to communicate and lead with transparency
  • Accountable for performance and results of department
  • Ability to assume additional responsibilities on own initiative.

Experience & Education
  • Requires minimum BA/BS in Biochemistry, Chemistry or related field with 10-15 years' experience in the biotech or pharmaceutical industry. Management experience in Quality Control required MS/MA.

Physical Requirements/Working Environment
  • Regular Laboratory environment with lab coats, safety glasses, 4-6hrs/day of standing while performing chemical test and able to stand for 4-6hrs/day.

Travel
  • No Travel requirement.

Disclaimer
The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.
We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.
Salary Description
$100,000 - $120,000 per year

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