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Pharmaceutical Qa Jobs in Reston, VA (NOW HIRING)

Granules

Quality Assurance Manager

Manassas, VA · On-site

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 ...

CAMRIS

Quality Assurance Manager

Silver Spring, MD · On-site

$128K - $173K/yr

PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next ... Manages QA at the WRAIR Pilot Bioproduction Facility (PBF) overseeing Good Manufacturing Practices ...

CAMRIS

Quality Assurance Manager

Silver Spring, MD · On-site

$128K - $173K/yr

PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next ... Responsibilities:Manages QA at the WRAIR Pilot Bioproduction Facility (PBF) overseeing Good ...

Granules

QA Technician- Warehouse Operations

Manassas, VA · On-site

$22 - $25/hr

Summary The QA Technician- Warehouse Operations for documentation at Granules Consumer Health ... Knowledge & Skills * cGMP compliance within the pharmaceutical manufacturing industry. * Writing ...

MicroCoders LLC

Entry level QA/BA

Reston, VA · On-site

Information Technology, Government, Insurance and Financial Services, Healthcare, Pharmaceutical ... MicroCoders LLC , is currently hiring Quality assurance analyst, and Business Analyst for ...

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Pharmaceutical Qa information

See Reston, VA salary details

$11

$48

$76

How much do pharmaceutical qa jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for pharmaceutical qa in Reston, VA is $48.59, according to ZipRecruiter salary data. Most workers in this role earn between $31.01 and $64.52 per hour, depending on experience, location, and employer.

What is a pharmaceutical QA?

Pharmaceutical QA (Quality Assurance) professionals are responsible for ensuring that pharmaceutical products are developed, manufactured, and distributed according to industry standards and regulatory requirements. Their main goal is to maintain product quality and safety by overseeing processes, conducting audits, and implementing quality management systems. They work closely with other departments to ensure compliance with Good Manufacturing Practices (GMP) and other regulations. QA professionals also investigate quality issues, review documentation, and facilitate continuous improvement to prevent future problems.

Is pharmaceutical QA a good career?

Pharmaceutical QA (Quality Assurance) is a stable career that involves ensuring drug manufacturing processes meet regulatory standards and quality requirements. It typically requires attention to detail, knowledge of Good Manufacturing Practices (GMP), and relevant certifications. The role offers opportunities for advancement and employment in the healthcare and biotech industries.

What is the difference between Pharmaceutical Qa vs Pharmaceutical Quality Control Analyst?

AspectPharmaceutical QaPharmaceutical Quality Control Analyst
CertificationsGMP, GDP, ISO certificationsGMP, GLP, ISO certifications
Work EnvironmentQuality assurance departments, regulatory complianceLaboratories, testing facilities
Primary FocusEnsuring quality processes and complianceTesting and analyzing raw materials and products

Pharmaceutical Qa professionals focus on maintaining quality standards through audits, documentation, and compliance, while Pharmaceutical Quality Control Analysts perform laboratory testing to verify product quality. Both roles are essential in the pharmaceutical industry and often work closely to ensure products meet regulatory requirements.

What are some common challenges faced by pharmaceutical QA professionals, and how can they be addressed?

Pharmaceutical QA professionals often encounter challenges such as staying up-to-date with evolving regulatory requirements, managing complex documentation, and ensuring consistent product quality across batches. To address these issues, QA teams typically participate in regular training, implement robust quality management systems, and foster close collaboration with production, R&D, and regulatory affairs departments. Effective communication and proactive problem-solving are also key to maintaining compliance and quickly resolving quality issues as they arise.

What are the key skills and qualifications needed to thrive as a pharmaceutical QA, and why are they important?

To thrive as a Pharmaceutical QA, you need a strong background in quality assurance processes, regulatory compliance, and a relevant scientific degree such as pharmacy, chemistry, or biology. Familiarity with Good Manufacturing Practices (GMP), quality management systems (QMS), and industry-standard audit tools or certifications like ISO 9001 is essential. Attention to detail, analytical thinking, and strong communication skills help professionals excel in identifying issues and ensuring adherence to standards. These skills are crucial for maintaining product safety, meeting regulatory requirements, and upholding a company’s reputation in the pharmaceutical industry.

How to become a pharmaceutical QA?

To become a pharmaceutical QA, candidates typically need a bachelor's degree in pharmacy, chemistry, or a related field, along with knowledge of Good Manufacturing Practices (GMP) and quality assurance processes. Gaining experience through internships or entry-level roles in pharmaceutical manufacturing or quality control is also important, and professional certifications like ASQ Certified Quality Auditor can enhance prospects.
What are popular job titles related to Pharmaceutical Qa jobs in Reston, VA? For Pharmaceutical Qa jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Pharmaceutical Qa jobs in Reston, VA look for? The top searched job categories for Pharmaceutical Qa jobs in Reston, VA are:
What cities near Reston, VA are hiring for Pharmaceutical Qa jobs? Cities near Reston, VA with the most Pharmaceutical Qa job openings:
Pharmaceutical Qa jobs near you
Infographic showing various Pharmaceutical Qa job openings in Reston, VA as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 7% Part Time, 6% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $101,065 per year, or $48.6 per hour.

Quality Assurance Manager

Granules Pharmaceuticals

Manassas, VA • On-site

Full-time

Re-posted 22 days ago

Job description

Job Type
Full-time
Description
*This is an Onsite Role**
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.
  • 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 Manassas, 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, Manassas, 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

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