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Qa Manufacturing Jobs in Washington (NOW HIRING)

Granules

Quality Assurance Manager

Manassas, VA · On-site

The QA Manager ensures compliance with cGMP and internal policies, procedures and specifications ... the pharmaceutical manufacturing industry. · Writing and maintaining cGMP documentation. · ...

PATTERNS

Quality Assurance Manager

Sterling, VA · On-site

Quality Assurance Manager Location: Sterling, VA Type: Fulltime Shift: 3PM to 12AM Key ... Support quality initiatives within a food manufacturing environment. * Identify quality risks ...

VB Spine

Quality Assurance Specialist

Leesburg, VA · On-site

$75K - $90K/yr

Quality Assurance Specialist Location: Leesburg, VA (10% Travel Required) Company: VB Spine Looking ... Develop and review Quality and Operational documents, including SOPs, manufacturing records, test ...

Northrop Grumman

Director Mission Assurance 2

Mclean, VA

$209K - $363K/yr

Ensuring the Quality/Mission Assurance, Manufacturing, and Engineering processes are consistent with industry capability maturity models and QMS standards (AS9100). Provide direct oversight in all ...

AstraZeneca

Director Quality Assurance

Rockville, MD

$174K - $262K/yr

Join us as a Director Quality Assurance, where you will lead and direct the Site Quality Assurance Operations at our Cell Therapy 9950 MCD Rockville manufacturing site. This role offers an ...

AstraZeneca

Director Quality Assurance

Rockville, MD

$174K - $262K/yr

Join us as a Director Quality Assurance , where you will lead and direct the Site Quality Assurance Operations at our Cell Therapy 9950 MCD Rockville manufacturing site. This role offers an ...

AstraZeneca

Director Quality Assurance

Rockville, MD · On-site

$174K - $262K/yr

Join us as a Director Quality Assurance , where you will lead and direct the Site Quality Assurance Operations at our Cell Therapy 9950 MCD Rockville manufacturing site. This role offers an ...

AstraZeneca

Director Quality Assurance

Rockville, MD · On-site

$174K - $262K/yr

Join us as a Director Quality Assurance , where you will lead and direct the Site Quality Assurance Operations at our Cell Therapy 9950 MCD Rockville manufacturing site. This role offers an ...

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All JobsQa Manufacturing JobsQa Manufacturing Jobs in Washington

Qa Manufacturing information

What is a QA manufacturing?

A QA Manufacturing job involves ensuring that products meet quality standards and regulatory requirements during the manufacturing process. Responsibilities typically include inspecting materials, monitoring production, conducting tests, and identifying defects or process improvements. QA professionals work closely with production teams to maintain consistency and compliance with industry standards. Their goal is to prevent defects, reduce waste, and enhance overall product quality before reaching customers.

What are some common challenges faced in a QA manufacturing role?

Common challenges in QA Manufacturing include identifying and correcting process inconsistencies, managing strict production deadlines, and ensuring compliance with company and regulatory quality standards. You may frequently interact with cross-functional teams such as production, engineering, and supply chain to troubleshoot quality issues or implement process improvements. Staying up to date with evolving technologies and standards, as well as adapting to changing product requirements, is essential for long-term success. Overcoming these challenges not only enhances product reliability but also contributes to a more efficient and collaborative workplace.

What are the key skills and qualifications needed to thrive in the QA manufacturing position, and why are they important?

To thrive as a QA Manufacturing professional, you need a solid understanding of quality assurance principles, manufacturing processes, and experience with inspection techniques, usually supported by a degree or certification in a relevant technical field. Familiarity with quality management systems (like ISO 9001), statistical process control (SPC), and tools such as calipers, micrometers, and ERP software is highly advantageous. Attention to detail, strong problem-solving abilities, and effective communication skills are crucial soft skills for this role. These attributes ensure the consistent production of high-quality products, improve process efficiency, and facilitate effective teamwork.

Is QA manufacturing a stressful job?

QA manufacturing can be stressful due to the responsibility of ensuring product quality and compliance with standards, often involving strict deadlines and attention to detail. The role requires focus, problem-solving skills, and sometimes working in fast-paced environments, but stress levels vary depending on the company and workload.

What is the role of QA in manufacturing?

The QA (Quality Assurance) role in manufacturing involves monitoring and inspecting products and processes to ensure they meet quality standards and specifications. QA professionals develop testing procedures, perform audits, and document findings to prevent defects and improve product reliability. They often use tools like inspection equipment and quality management systems to maintain consistent product quality.

What are popular job titles related to Qa Manufacturing jobs in Washington?

For Qa Manufacturing jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Qa Manufacturing jobs in Washington look for?

The top searched job categories for Qa Manufacturing jobs in Washington are:

Qa Manufacturing jobs near you
Infographic showing various Qa Manufacturing job openings in Washington as of August 2026, with employment types broken down into 86% Full Time, 3% Part Time, 2% Temporary, 7% Contract, and 2% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution.

Quality Assurance Manager

Granules Pharmaceuticals

Manassas, VA • On-site

Full-time

Re-posted 18 days ago

Key responsibilities

  • Manage and ensure compliance with cGMP, FDA regulations, and internal policies across quality operations.

  • Oversee inspection, documentation, and release of components, bulk, and final products to meet lead times and quality standards.

  • Lead communication and resolution of quality issues such as complaints, investigations, change control, and CAPAs among departments.

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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