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Qa Manufacturing Jobs in Washington (NOW HIRING)

Caraballo Consulting & Associates L

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QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

Support quality assurance activities associated with transferring and starting up manufacturing operations at the new site. * Review, execute, and approve validation documentation, including ...

Caraballo Consulting & Associates L

Be Seen First

QA Manufacturing Engineer - Medical Device

Sterling, VA · On-site

$40 - $80/hr

Support quality assurance activities associated with transferring and starting up manufacturing operations at the new site. * Review, execute, and approve validation documentation, including ...

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 ...

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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.

QA Manufacturing Engineer - Medical Device

Caraballo Consulting & Associates L

Sterling, VA • On-site

$40 - $80/hr

Contractor

Posted 19 days ago

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Job description

We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company.  The perfect candidate will perform the following activities:

Key Responsibilities:

    • Support quality assurance activities associated with transferring and starting up manufacturing operations at the new site.
    • Review, execute, and approve validation documentation, including protocols, test scripts, test data, and final reports.
    • Provide QA oversight for process validation activities to ensure processes are qualified, controlled, and appropriately documented.
    • Support equipment qualification efforts, including IQ, OQ, and PQ activities for manufacturing equipment and related systems.
    • Partner with Manufacturing, Engineering, Validation, and Quality teams to ensure validation deliverables are completed on time and in compliance with applicable procedures and regulations.
    • Assess validation packages for completeness, accuracy, traceability, and adherence to GMP and medical device quality system requirements.
    • Support investigation and resolution of validation-related deviations, discrepancies, and change controls.
    • Generate, review, and approve validation summary reports and supporting documentation for management and quality records.                  
    • Support QA activities associated with the QMS integration of 2 companies.
    • Modify SOPs to complete QMS integration.
    • Complete Change Control activities.
    • Complete the bulk download of documents and records from a Quality Management System.

   Required Qualifications:

  • Bachelor’s degree in Engineering, Quality, Life Sciences, or a related technical discipline, or equivalent relevant experience.
  • Experience in the medical device industry within Quality Assurance, Validation, Manufacturing Quality, or a closely related function.
  • Strong working knowledge of process validation, equipment qualification, and GMP requirements in a regulated manufacturing environment.
  • Demonstrated experience reviewing and approving validation documentation and technical reports.
  • Familiarity with manufacturing operations and the practical application of quality requirements on the production floor.
  • Ability to work independently while coordinating effectively with cross-functional stakeholders.
  • Strong technical writing, documentation review, and problem-solving skills.
  • Excellent attention to detail and ability to manage multiple priorities within a time-bound project.

Company Description

We are a specialized Global staffing firm that works for Fortune 500 companies in the Medical Device, Pharmaceutical, and Biotec industries, finding qualified personnel.