87 QA Engineering Jobs in Washington, DC, United States

Role highlights

• Experience developing, implementing, maintaining, or improving software quality processes or procedures is required.
• Guide software R&D teams through applicable Quality Management System processes, procedures, and documentation requirements.

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• Experience in product quality, reliability, or product engineering for PCB, PCBA and Electronic assembly & Servers.
• Develop and implement supplier quality management strategies that drive manufacturing excellence, product reliability, and compliance with…

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• This position reports directly to Vice President of Quality Assurance/Quality Control (or designated representative in QAQC service center).
• On behalf of VP of Quality Assurance/Quality Control, this position is directly responsible for documenting, managing, implementing and ins…

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• Essential Functions: Design and execute testing strategies for Android and iOS applications and firmware across a wide range of devices…
• Our tight-knit interdisciplinary teams generate thoughtful capability designs and incremental feature releases that reliably deliver world-…

Role highlights

• Essential Functions: Design and execute testing strategies for Android and iOS applications and firmware across a wide range of devices…
• Our tight-knit interdisciplinary teams generate thoughtful capability designs and incremental feature releases that reliably deliver world-…

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• These Quality Engineers will support the development and implementation of mission assurance requirements over the entire project life cycl…
• These Quality Engineers will also focus on supplier surveillance and inspections.

Role highlights

• The QA/QC Manager will work with QA/QC professionals across MEP trade disciplines, General Contractor, and Owner QAQC Leadership to create…
• QA/QC Engineer - Summary: This role is responsible for the implementation and management of Bureau Veritas Primary Integration's (BVPI) Qua…

Role highlights

• Review inspection reports for compliance Assist the site stakeholders in the administration and oversight of the quality control program Pr…
• The QA/QC Manager will work with QA/QC professionals across MEP trade disciplines, General Contractor, and Owner QAQC Leadership to create…

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• Support engineering and Clinical/Commercial GMP runs at assembly sites.
• Primary responsibilities will include: 1) Device/Combination Product Assembly Technical Leadership: Give to the operation of a fill-finish/…

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• Serve as the Submission Management lead for assigned programs, driving submission strategy discussions and ensuring alignment across Cell T…
• Experience supporting Cell Therapy, Gene Therapy, ATMPs, biologics, or other advanced therapies.

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• On-site Quality Assurance / Quality Control for assigned construction projects Witnessing and reviewing site inspections Ensure general con…
• Review inspection reports for compliance Assist the site stakeholders in the administration and oversight of the quality control program Pr…

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• Key Responsibilities Regulatory Document Authoring Author and manage FDA submissions, including PMTAs, MRTPAs, amendments, supplements, pos…
• Serve as a regulatory subject matter expert on cross-functional project teams and monitor evolving regulatory requirements.

Role highlights

• Principal responsibilities will include but are not limited to: The QC/QA Manager will serve as the senior quality authority responsible…
• The QC/QA Manager will develop comprehensive method statements, lead quality initiatives, and ensure all work complies with applicable code…

Role highlights

• EDUCATION, EXPERIENCE & SKILLS 2+ years of Quality Control and/or Quality Assurance experience.
• Explore Opportunities Today This position is responsible for coordinating and overseeing outsourced post-closing quality control activities…

Role highlights

• The QA/QC Manager will work with QA/QC professionals across MEP trade disciplines, General Contractor, and Owner QAQC Leadership to create…
• QA/QC Manager I - Summary: This role is responsible for the implementation and management of Bureau Veritas Primary Integration's (BVPI)…

Role highlights

• Key Responsibilities You will work in a laboratory environment focused on vaccine drug product development, supporting programs from early…
• Desirable Skills & Experience Process Engineering : Experience with unit operations relevant to vaccines (e.g., homogenization/emulsificati…

Role highlights

• The Associate Director will be responsible for providing quantitative measurement support for the execution of patient-centered measurement…
• Participate in or lead processes for data evaluation, such as triage, adverse event interpretation, or anomaly recognition, ensuring high-q…

Role highlights

• Senior Scientist, Vaccine Drug Product Development Introduction to the Role Join our Vaccines Drug Product Development team to shape the…
• Key Responsibilities You will work in a laboratory environment focused on vaccine drug product development, supporting programs from early…

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• Experience authoring or providing strategic leadership for protocol development, CRF design, safety monitoring plans, and clinical study co…
• You will be accountable for the ongoing benefit-risk assessment, safety strategy, signal detection and evaluation, regulatory safety delive…

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• In this role, you will operate at the nexus of the health ecosystem, technological advancement, and regulatory expertise to steer…
• Experience with medical device standards and software as a medical device frameworks.

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• Desirable: Substantive and progressively responsible professional experience in pharmaceutical regulatory systems, including regulatory fun…
• Strong leadership and strategic advisory skills in medicines regulation and regulatory decision-making.

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• Your Role: As the Quality Assurance Specialist 3, you will perform a variety of tasks within the Quality Assurance department…
• Works with cross-functional teams and builds networks within QA and Operations departments.

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• A minimum of FOUR (4) years of active medical device development experience with at least TWO (2) years of direct…
• Support engineering research and development efforts focused on next-generation catheter systems, guidewires, and accessory electronics.

Role highlights

• Your contribution: Develop and implement strategic frameworks for raw material knowledge transfer and lifecycle management Lead cross-funct…
• Working closely with cross-functional teams, you’ll be at the forefront of material science innovation and regulatory compliance, contribut…

Role highlights

• Quality management/quality improvement experience.
• Job duties include but may not be limited to: Supports the Quality and Patient Safety Program through participation in Root…