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Quality Control Pharma Jobs in Virginia (NOW HIRING)

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 ...

Granules

Manager, Analytical R&D

Chantilly, VA · On-site

$100K - $130K/yr

... pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through ... Plan and Manage In-process release testing for exhibit batches and coordinate with Quality Control ...

Granules Pharmaceuticals

Trainee Engineer

Chantilly, VA · On-site

... pharma company in the US! With our sites in Chantilly and Manassas, Virginia, we have R&D through ... Review production, quality control and maintenance reports and statistics to plan and modify ...

Stantec

Senior Process Engineer - Industrial Water

Richmond, VA · On-site

$102K - $133K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Municipal, Manufacturing, Energy, Power, Food and Beverage, Hi-Tech, Mining, and Pharma. The role ... Conduct and/or coordinate quality assurance and quality control on assigned projects and facilitate ...

Stantec

Senior Process Engineer - Industrial Water

Richmond, VA · On-site

$103K - $133K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Municipal, Manufacturing, Energy, Power, Food and Beverage, Hi-Tech, Mining, and Pharma. The role ... Conduct and/or coordinate quality assurance and quality control on assigned projects and facilitate ...

Catalent, Inc.

Maintenance Mechanic

Manassas, VA · On-site

$25 - $32/hr

  • Life

  • PTO

... 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 ...

Bilfinger

Superintendent - Stafford, VA

Stafford, VA

... chemicals, pharma, and oil & gas. Bilfinger North America has a national reach spanning from ... Control all job site operations for compliance with contract requirements, noise and dust control ...

Bilfinger

Superintendent - Stafford, VA

Stafford, VA · On-site

... chemicals, pharma, and oil & gas. Bilfinger North America has a national reach spanning from ... Control all job site operations for compliance with contract requirements, noise and dust control ...

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Showing results 21-40

All JobsQuality Control Pharma JobsQuality Control Pharma Jobs in Virginia

Quality Control Pharma information

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 are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

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 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 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.

Is quality control pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It offers stable employment, opportunities for advancement, and requires attention to detail, knowledge of laboratory techniques, and often certifications such as GMP training.

What is the role of quality control in pharma?

The role of quality control in pharma involves testing and inspecting raw materials, in-process samples, and finished products to ensure they meet safety, efficacy, and quality standards. QC professionals use analytical techniques and follow Good Manufacturing Practices (GMP) to identify and prevent defects, supporting regulatory compliance and product consistency.

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 August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

Associate Manager/Manager, Quality Assurance

Granules Pharmaceuticals

Chantilly, VA • On-site

$115K/yr

Full-time

Re-posted 21 days ago

Job description

Job Type
Full-time
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.
The QA Manager ensures compliance with cGMP and internal policies, procedures and specifications. This position is responsible for performing documentation for all quality system functions in accordance with cGMP and related company SOP's, state, federal and local laws as applicable. This person should be knowledgeable of cGMP requirements, FDA regulations and ICH guidelines.
Job Duties & Responsibilities
  • The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements.
  • Managing all quality operations to include inspection of components, bulk, and final products for the Chantilly, VA, ensuring release lead times are met with timely product disposition.
  • Ensure that the facility is meeting all training requirements.
  • Lead the communication of open quality document notification and resolution between all departments regarding Complaints, Investigations, Change Control, CAPA's (including verification of CAPA's) and other quality documents as needed.
  • Manage and maintain audit inspections (Internal and External) for the site.
  • Responsible for supporting the preparation, review, processing, and approval of various validation documents as application for the Granules, Chantilly, facility.
  • Provide QA support, review and approval for relevant documents including relevant procedures, batch records, specifications, stability reports, technical reports (i.e., Qualification, Validation, Transportation.), trend reports, Annual Product Quality Reviews and other documents as needed.
  • Responsible for performance and development of all Quality Assurance staff through mentoring and focusing on personal and professional growth.
  • Work with Quality leadership team for proactive succession planning and a high-performance culture through people.
  • Guide and lead by setting realistic personal goals for staff and provide regularly scheduled feedback throughout the year.
  • Provide the means for incorporating the necessary tools, equipment, and methods into the new and existing processes aimed at continuous improvement.
  • Implementation Quality management system tools and their compliance.
  • Development and execution of quality training modules for the organization.
  • Ensure staff receives appropriate knowledge and skill development and growth opportunities
  • Work with Regulatory Affairs to supply information needed for FDA filings.
  • Other duties as assigned by management.

Requirements
Knowledge & Skills
  • Expert-level knowledge of the FDA guidance for Industry, Title 21 of the Code of Federal Regulations and Compendia (USP/EP/BP/etc...)
  • cGMP compliance within the pharmaceutical manufacturing industry.
  • Writing and maintaining cGMP documentation.
  • Analyze data/information and resolve complex issues.
  • Verbal and written communication skills.
  • Work and communicate with cross-functional teams.
  • Multiple priorities and re-prioritize tasks.
  • Strong computer skills and working knowledge of Microsoft Office Suite and Adobe
  • Demonstrated ability to work on complex assignments in collaboration with various departments.

Experience & Education
  • Bachelor's degree in the life sciences (or equivalent work experience) minimum of 6+ years in a QA role within the pharmaceutical industry
  • Master's degree with 4+ years of pharmaceutical manufacturing experience and at least 3 years of those years in a progressive challenging QA department in the pharmaceutical industry.

Physical Requirements/Working Environment
  • While performing the duties of this job, the employee is regularly required to, stand, sit, talk, hear, and use hands and fingers to operate a computer and telephone keyboard.
  • Specific vision abilities required by this job include close vision requirements due to computer work.
  • Ability to sit at a computer terminal for an extended period of time.
  • Light to moderate lifting up to 10-15 lbs is required.
  • Ability to work in a confined area

We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.
Salary Description
$115K/yr + Bonus

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