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Support Quality Associate Jobs in Virginia (NOW HIRING)

Laminate Technologies

QUALITY INSPECTOR

Ridgeway, VA · On-site

Support quality assurance activities such as First Article Inspections, Gemba walks, and internal ... Technical training or associate degree in a quality-related field preferred. * Minimum 1-3 years of ...

Laminate Technologies Inc

QUALITY INSPECTOR

Ridgeway, VA · On-site

$19/hr

Support quality assurance activities such as First Article Inspections, Gemba walks, and internal ... Technical training or associate degree in a quality-related field preferred. * Minimum 1-3 years of ...

Laminate Technologies Inc

QUALITY INSPECTOR

Ridgeway, VA · On-site

Support quality assurance activities such as First Article Inspections, Gemba walks, and internal ... Technical training or associate degree in a quality-related field preferred. * Minimum 1-3 years of ...

Mpr Associates, Inc.

Quality Engineer

Alexandria, VA · On-site

$77K - $99K/yr

Assemble the information needed to support management review meetings, prepare the resulting report ... About MPR Founded in 1964, MPR Associates provides independent engineering and consulting services ...

Mpr Associates, Inc.

Quality Engineer

Alexandria, VA

$77K - $99K/yr

Assemble the information needed to support management review meetings, prepare the resulting report ... About MPR Founded in 1964, MPR Associates provides independent engineering and consulting services ...

MPR Associates, Inc.

Quality Engineer

Alexandria, VA · On-site

$76K - $99K/yr

Assemble the information needed to support management review meetings, prepare the resulting report ... About MPR Founded in 1964, MPR Associates provides independent engineering and consulting services ...

Mpr Associates, Inc.

Quality Engineer

Alexandria, VA · On-site

$77K - $99K/yr

Assemble the information needed to support management review meetings, prepare the resulting report ... About MPR Founded in 1964, MPR Associates provides independent engineering and consulting services ...

PerkinElmer

Associate Scientist, Quality

Richmond, VA · On-site

The Associate Scientist, Quality supports quality assurance and quality control operations for the insourced laboratory team as part of an End-to-End (E2E) Laboratory Modernization Program. Depending ...

PerkinElmer

The Associate Scientist, Quality supports quality assurance and quality control operations for the insourced laboratory team as part of an End-to-End (E2E) Laboratory Modernization Program. Depending ...

Alfa Laval Mid Europe GmbH

Quality Engineer

Richmond, VA · On-site

$85K - $90K/yr

You'll lead and support quality improvement projects and activities, actively participate in the ... Our benefits-eligible associates enjoy healthcare, dental and vision plans, a robust wellness ...

New

Alfa Laval

Quality Engineer

Richmond, VA · On-site

$85K - $90K/yr

You'll lead and support quality improvement projects and activities, actively participate in the ... Our benefits-eligible associates enjoy healthcare, dental and vision plans, a robust wellness ...

Marvin

Spring 2027 Quality Engineering Intern

Roanoke, VA · On-site

$21.50/hr

Support "Quality at the Source" initiatives via assisting in integration of Quality checks into production processes. * Collaborate with and train associates on Quality specifications and processes ...

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QA Manufacturing Engineer - Medical Device

Sterling, VA • On-site

Caraballo Consulting & Associates L
See more jobs at Caraballo Consulting & Associates Lexternal

$40 - $80/hr

Contractor

Posted 27 days ago

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.